摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

ethyl 4-(furan-2-yl)-2,7,7-trimethyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate

中文名称
——
中文别名
——
英文名称
ethyl 4-(furan-2-yl)-2,7,7-trimethyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate
英文别名
Ethyl 4-(furan-2-yl)-5-hydroxy-2,7,7-trimethyl-4,6,7,8-tetrahydroquinoline-3-carboxylate;ethyl 4-(furan-2-yl)-2,7,7-trimethyl-5-oxo-1,4,6,8-tetrahydroquinoline-3-carboxylate
ethyl 4-(furan-2-yl)-2,7,7-trimethyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate化学式
CAS
——
化学式
C19H23NO4
mdl
——
分子量
329.396
InChiKey
WKOSWJZFFXTFHN-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    2.7
  • 重原子数:
    24
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.47
  • 拓扑面积:
    68.5
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    ethyl 4-(furan-2-yl)-2,7,7-trimethyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate叔丁基过氧化氢 、 sodium dithionite 作用下, 以 乙酸乙酯 为溶剂, 反应 7.0h, 以62%的产率得到
    参考文献:
    名称:
    A new oxidation system for the oxidation of Hantzsch-1,4-dihydropyridines and polyhydroquinoline derivatives under mild conditions
    摘要:
    已开发出一种氧化系统,通过氧化1,4-二氢吡啶和多羟基喹啉衍生物,可以高产率合成吡啶衍生物。
    DOI:
    10.1039/c5ra20977c
  • 作为产物:
    描述:
    糠醛乙酰乙酸乙酯5,5-二甲基-1,3-环己二酮 在 ammonium acetate 作用下, 以 neat (no solvent) 为溶剂, 反应 0.33h, 以92%的产率得到ethyl 4-(furan-2-yl)-2,7,7-trimethyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate
    参考文献:
    名称:
    具有离子-液体骨架的周期性介孔有机二氧化硅负载锰:用于不对称Hantzsch反应的高效可回收纳米催化剂
    摘要:
    生物活性取代polyhydroquinoline衍生物的绿色和快速合成的有效方法通过描述了在无溶剂条件下使用基于离子液体的周期性介孔有机二氧化硅负载的锰(Mn @ PMO-IL)催化剂进行的不对称Hantzsch反应。该催化剂在中等反应条件和短时间内制备一组不同的聚氢喹啉衍生物具有很高的反应活性和选择性。此外,在不显着降低反应性和产率的情况下,催化剂也被回收并重复使用了几次。回收的催化剂的氮吸附-解吸和透射电子显微镜显着证明了在所应用的反应条件下催化剂的高稳定性和耐久性。此外,与传统方法相比,该方法始终显示出反应时间短,催化剂用量低,收率高,
    DOI:
    10.1039/c4ra12673d
点击查看最新优质反应信息

文献信息

  • Polyhydroquinolines: 1-sulfopyridinium chloride catalyzed an efficient one-pot multicomponent synthesis via Hantzsch condensation under solvent-free conditions
    作者:B. Sakram、B. Sonyanaik、K. Ashok、S. Rambabu
    DOI:10.1007/s11164-016-2559-y
    日期:2016.10
    construction of polyhydroquinoline derivatives via one-pot, four-component Hantzsch condensation of various aldehydes, dimedone, ethyl acetoacetate, and ammonium acetate in the presence of an ionic liquid, 1-sulpopyridinium chloride, as a catalyst under solvent-free conditions. This methodology has an advantage of high yields, short reaction times, a clean reaction profile, and reusability of the catalyst.
    摘要研究了 一种简单高效的方法,在离子液体1-磺基吡啶鎓氯化物存在下,通过一锅四组分的多种醛,二甲酮,乙酰乙酸乙酯和乙酸铵的汉茨缩合反应来构建聚氢喹啉衍生物。 ,在无溶剂条件下用作催化剂。该方法的优点是高产率,短反应时间,干净的反应曲线和催化剂的可重复使用性。 图形概要
  • Urea as an Ammonia Surrogate in the Hantzsch’s Synthesis of Polyhydroquinolines / 1,4-dihydropyridines under Green Reaction Conditions
    作者:G. Dhananjaya、Akula Raghunadh、P. Mahesh Kumar、S. Pulla Reddy、V. Narayana Murthy、Venkateswara Rao Anna、Manojit Pal
    DOI:10.2174/1570178617999200713144504
    日期:2021.3
    <p>Synthesis of polyhydroquinolines via Hantzsch’s multicomponent reaction (MCR) involves the use of a hygroscopic and moderately toxic ammonium salt as one of the key reactants. In our effort, we have found urea as an effective ammonia surrogate when the MCR was performed in the presence of sulphonic acid-functionalized Wang resin (Wang-OSO<sub>3</sub>H) as a polymeric and recoverable acidic catalyst under green conditions. Urea is relatively less hygroscopic/toxic than the commonly used ammonium salts used in this MCR. The methodology afforded a range of polyhydroquinolines in good yields. Depending on the nature of reaction conditions employed, the MCR afforded Biginelli product or 1,4-DHPs when the use of 1,3-diketone was omitted.</p> </sec></div> <div class="value-text ch"><p>通过汉奇多组分反应(MCR)合成聚氢喹啉,涉及使用一种吸湿性和中等毒性的铵盐作为关键反应物之一。在我们的努力中,我们发现尿素在存在磺酸基功能化王树脂(Wang-OSO<sub>3</sub>H)作为聚合物和可回收的酸性催化剂的条件下,作为有效的氨替代品。尿素比这种MCR中常用的铵盐相对更不易吸湿/有毒。该工艺提供了一系列高产率的聚氢喹啉。根据所用反应条件的性质,当省略使用1,3-二酮时,MCR会生成Biginelli产物或1,4-DHPs。</p></div> </div> </li> <li class="feature-list-item"> <div class="content-title">Molybdenum- and Tungsten-Based Coordination Polymers as Catalysts for an Efficient and Rapid Synthesis of Hexahydro-5-oxoquinoline-3-carboxylates and 1,4-Dihydropyridine-3,5-dicarboxylates</div> <div class="value"> <div class="value-text"> <span>作者:</span>Biswanath Das、Malampati Srilatha、Boyapati Veeranjaneyulu、Boddu Shashi Kanth </div> <div class="value-text"> <span>DOI:</span>10.1002/hlca.201000354 </div> <div class="value-text"> <span>日期:</span>2011.5 </div> <div class="value-text en">rapidly (2 min) in the presence of <span style='color:#ff0000'>molybdenum</span>‐ and tungsten‐based coordination <span style='color:#ff0000'>polymers</span> [M(Bu3Sn)2O4)]n (M=Mo or W) as <span style='color:#ff0000'>catalysts</span> (Schemes 1 and 2; Tables 2 and 3). The products were formed at room temperature in excellent yields (90–98%). The <span style='color:#ff0000'>catalysts</span> worked under heterogeneous conditions and were recyclable. The earlier reports for the application of these <span style='color:#ff0000'>polymers</span> to conduct organic synthesis are</div> <div class="value-text ch">在基于钼和钨的配位聚合物[M(Bu 3 Sn)2 O 4)] n(M = Mo或W)作为催化剂(方案1和2;表2和3)。产品在室温下以优异的收率(90–98%)形成。催化剂在非均相条件下工作且可回收。这些聚合物用于进行有机合成的早期报道是有限的。本方法探索了这些催化剂的新的有用的应用。</div> </div> </li> <li class="feature-list-item"> <div class="content-title">Synthesis, characterization and heterogeneous catalytic application of a nickel(II) Schiff base complex immobilized on MWCNTs for the Hantzsch four-component condensation</div> <div class="value"> <div class="value-text"> <span>作者:</span>Jamshid Rakhtshah、Sadegh Salehzadeh、Mohammad Ali Zolfigol、Saeed Baghery </div> <div class="value-text"> <span>DOI:</span>10.1080/00958972.2016.1253068 </div> <div class="value-text"> <span>日期:</span>2017.1.17 </div> <div class="value-text en">highly <span style='color:#ff0000'>efficient</span> heterogeneous catalyst was synthesized and characterized by IR, X-ray diffraction patterns, scanning electron microscopy, energy-dispersive X-ray spectroscopy, inductively coupled plasma, elemental analysis, and thermal gravimetric analysis. Then a facile and environmentally benign procedure was developed for <span style='color:#ff0000'>synthesis</span> of <span style='color:#ff0000'>polyhydroquinoline</span> derivatives via <span style='color:#ff0000'>Hantzsch</span> <span style='color:#ff0000'>one-pot</span> condensation</div> <div class="value-text ch">摘要 合成了一种固定在多壁碳纳米管 (MWCNTs) 表面的镍 (II) Schiff 碱配合物作为一种高效的多相催化剂,并通过 IR、X 射线衍射图、扫描电子显微镜、能量色散 X 射线光谱进行表征。 、电感耦合等离子体、元素分析和热重分析。然后,在上述合成催化剂的存在下,在无溶剂条件下,通过芳香醛、1,3-二酮、乙酰乙酸乙酯和乙酸铵的 Hantzsch 一锅缩合反应,开发了一种简便且环境友好的方法合成聚氢喹啉衍生物。该方案具有催化剂稳定性、易得性、可回收性和环保性,实验和后处理程序简单等优点,并且产量也很高。考虑到模型反应的无溶剂条件以及温度、时间和产率,这里报道的纳米催化剂是迄今为止报道的用于合成聚氢喹啉的最佳催化剂之一。</div> </div> </li> <li class="feature-list-item"> <div class="content-title">Synthesis and biological evaluation of new series 1,4-dihydropyridines</div> <div class="value"> <div class="value-text"> <span>作者:</span>Ramin Ghorbani-Vaghei、Seyedeh Mina Malaekehpoor、Parisa Hasanein、Roya Karamyan、Mostafa Asadbegy </div> <div class="value-text"> <span>DOI:</span>10.1007/s11164-015-2310-0 </div> <div class="value-text"> <span>日期:</span>2016.5 </div> <div class="value-text en">Abstract N , N , N ′, N ′-Tetrachlorobenzene-1,3-disulfonamide and poly( N , N ′-dichloro- N -ethyl-benzene-1,3-disulfonamide) are <span style='color:#ff0000'>new</span> catalysts promoted by one-pot, facile and four-component <span style='color:#ff0000'>synthesis</span> of <span style='color:#ff0000'>new</span> substituted 1,4-dihydropyridine derivatives from the reaction of ammonium acetate, aldehydes and various 1,3-dicarbonyl compounds with good to high yields at room temperature under mild conditions</div> <div class="value-text ch">摘要 N , N , N ', N'- 四氯苯-1,3-二磺酰胺和聚( N , N'- 二氯 -N -乙基-苯-1,3-二磺酰胺)是通过乙酸铵,醛和各种1,3-二羰基的反应通过一锅,简便和四组分合成新的取代的1,4-二氢吡啶衍生物而开发的新型催化剂在室温和温和条件下具有良好到高收率的化合物。评价所有合成的化合物的抗菌和抗氧化活性。确定了对四种革兰氏阳性和阴性细菌的抗菌活性,并通过2,2-二苯基-1-吡啶并肼基自由基清除作用评估了抗氧化活性。生物测定结果表明,合成的1,4-二氢吡啶衍生物具有有效的抗氧化和抗菌作用。 图形摘要 新系列二氢吡啶的合成和生物学评价。</div> </div> </li> </ul> <a href="https://chem.molaid.com/material/detail?source=UserSourcePortal&id=310166br9199c6e048M0&inchikey=WKOSWJZFFXTFHN-UHFFFAOYSA-N" target="_blank" rel="nofollow" class="view-more">查看更多</a> </div> <div class="module" id="tongleihuahewu"> <h3 class="module-title"><i class="iconfont icon-tongleihuahewu"></i>同类化合物</h3> <div class="compounds-list"> <a target="_blank" href="https://www.molaid.com/MS_6" class="compound-item" title="(反式)-4-壬烯醛">(反式)-4-壬烯醛</a> <a target="_blank" href="https://www.molaid.com/MS_14" class="compound-item" title="(s)-2,3-二羟基丙酸甲酯">(s)-2,3-二羟基丙酸甲酯</a> <a target="_blank" href="https://www.molaid.com/MS_17" class="compound-item" title="([1-(甲氧基甲基)-1H-1,2,4-三唑-5-基](苯基)甲酮)">([1-(甲氧基甲基)-1H-1,2,4-三唑-5-基](苯基)甲酮)</a> <a target="_blank" href="https://www.molaid.com/MS_19" class="compound-item" title="(Z)-4-辛烯醛">(Z)-4-辛烯醛</a> <a target="_blank" href="https://www.molaid.com/MS_32" class="compound-item" title="(S)-氨基甲酸酯β-D-O-葡糖醛酸">(S)-氨基甲酸酯β-D-O-葡糖醛酸</a> <a target="_blank" href="https://www.molaid.com/MS_37" class="compound-item" title="(S)-3-(((2,2-二氟-1-羟基-7-(甲基磺酰基)-2,3-二氢-1H-茚满-4-基)氧基)-5-氟苄腈">(S)-3-(((2,2-二氟-1-羟基-7-(甲基磺酰基)-2,3-二氢-1H-茚满-4-基)氧基)-5-氟苄腈</a> <a target="_blank" href="https://www.molaid.com/MS_54" class="compound-item" title="(R)-氨基甲酸酯β-D-O-葡糖醛酸">(R)-氨基甲酸酯β-D-O-葡糖醛酸</a> <a target="_blank" href="https://www.molaid.com/MS_188" class="compound-item" title="(2,5-二氟苯基)-4-哌啶基-甲酮">(2,5-二氟苯基)-4-哌啶基-甲酮</a> <a target="_blank" href="https://www.molaid.com/MS_232" class="compound-item" title="龙胆苦苷">龙胆苦苷</a> <a target="_blank" href="https://www.molaid.com/MS_238" class="compound-item" title="龙胆二糖甲乙酮氰醇(P)">龙胆二糖甲乙酮氰醇(P)</a> <a target="_blank" href="https://www.molaid.com/MS_239" class="compound-item" title="龙胆二糖丙酮氰醇(P)">龙胆二糖丙酮氰醇(P)</a> <a target="_blank" href="https://www.molaid.com/MS_241" class="compound-item" title="龙胆三糖">龙胆三糖</a> <a target="_blank" href="https://www.molaid.com/MS_244" class="compound-item" title="龙涎酮">龙涎酮</a> <a target="_blank" href="https://www.molaid.com/MS_250" class="compound-item" title="齐罗硅酮">齐罗硅酮</a> <a target="_blank" href="https://www.molaid.com/MS_254" class="compound-item" title="齐留通beta-D-葡糖苷酸">齐留通beta-D-葡糖苷酸</a> <a target="_blank" href="https://www.molaid.com/MS_302" class="compound-item" title="鼠李糖">鼠李糖</a> <a target="_blank" href="https://www.molaid.com/MS_320" class="compound-item" title="黑芥子苷单钾盐">黑芥子苷单钾盐</a> <a target="_blank" href="https://www.molaid.com/MS_325" class="compound-item" title="黑海棉酸钠盐">黑海棉酸钠盐</a> <a target="_blank" href="https://www.molaid.com/MS_331" class="compound-item" title="黑木金合欢素">黑木金合欢素</a> <a target="_blank" href="https://www.molaid.com/MS_333" class="compound-item" title="黑曲霉三糖">黑曲霉三糖</a> <a target="_blank" href="https://www.molaid.com/MS_335" class="compound-item" title="黑介子苷">黑介子苷</a> <a target="_blank" href="https://www.molaid.com/MS_472" class="compound-item" title="黄尿酸8-O-葡糖苷">黄尿酸8-O-葡糖苷</a> <a target="_blank" href="https://www.molaid.com/MS_511" class="compound-item" title="麻西那霉素II">麻西那霉素II</a> <a target="_blank" href="https://www.molaid.com/MS_518" class="compound-item" title="麦迪霉素">麦迪霉素</a> <a target="_blank" href="https://www.molaid.com/MS_582" class="compound-item" title="麦芽糖脎">麦芽糖脎</a> <a target="_blank" href="https://www.molaid.com/MS_584" class="compound-item" title="麦芽糖基海藻糖">麦芽糖基海藻糖</a> <a target="_blank" href="https://www.molaid.com/MS_587" class="compound-item" title="麦芽糖1-磷酸酯">麦芽糖1-磷酸酯</a> <a target="_blank" href="https://www.molaid.com/MS_589" class="compound-item" title="麦芽糖">麦芽糖</a> <a target="_blank" href="https://www.molaid.com/MS_591" class="compound-item" title="麦芽四糖醇">麦芽四糖醇</a> <a target="_blank" href="https://www.molaid.com/MS_592" class="compound-item" title="麦芽四糖">麦芽四糖</a> <a target="_blank" href="https://www.molaid.com/MS_593" class="compound-item" title="麦芽十糖">麦芽十糖</a> <a target="_blank" href="https://www.molaid.com/MS_594" class="compound-item" title="麦芽六糖">麦芽六糖</a> <a target="_blank" href="https://www.molaid.com/MS_595" class="compound-item" title="麦芽五糖水合物">麦芽五糖水合物</a> <a target="_blank" href="https://www.molaid.com/MS_596" class="compound-item" title="麦芽五糖">麦芽五糖</a> <a target="_blank" href="https://www.molaid.com/MS_597" class="compound-item" title="麦芽五糖">麦芽五糖</a> <a target="_blank" href="https://www.molaid.com/MS_598" class="compound-item" title="麦芽五糖">麦芽五糖</a> <a target="_blank" href="https://www.molaid.com/MS_599" class="compound-item" title="麦芽三糖醇">麦芽三糖醇</a> <a target="_blank" href="https://www.molaid.com/MS_600" class="compound-item" title="麦芽三糖">麦芽三糖</a> <a target="_blank" href="https://www.molaid.com/MS_601" class="compound-item" title="麦芽三糖">麦芽三糖</a> <a target="_blank" href="https://www.molaid.com/MS_602" class="compound-item" title="麦芽三塘水合">麦芽三塘水合</a> <a target="_blank" href="https://www.molaid.com/MS_603" class="compound-item" title="麦芽七糖水合物">麦芽七糖水合物</a> <a target="_blank" href="https://www.molaid.com/MS_604" class="compound-item" title="麦芽七糖">麦芽七糖</a> <a target="_blank" href="https://www.molaid.com/MS_611" class="compound-item" title="麦法朵">麦法朵</a> <a target="_blank" href="https://www.molaid.com/MS_619" class="compound-item" title="麦可酚酸-酰基-Β-D-葡糖苷酸">麦可酚酸-酰基-Β-D-葡糖苷酸</a> <a target="_blank" href="https://www.molaid.com/MS_621" class="compound-item" title="麦利查咪">麦利查咪</a> <a target="_blank" href="https://www.molaid.com/MS_627" class="compound-item" title="麝香酮">麝香酮</a> <a target="_blank" href="https://www.molaid.com/MS_641" class="compound-item" title="鹤草酚">鹤草酚</a> <a target="_blank" href="https://www.molaid.com/MS_690" class="compound-item" title="鸢尾酚酮 3-C-beta-D-吡喃葡萄糖苷">鸢尾酚酮 3-C-beta-D-吡喃葡萄糖苷</a> <a target="_blank" href="https://www.molaid.com/MS_705" class="compound-item" title="鸟苷5'-硫代二磷酸酯">鸟苷5'-硫代二磷酸酯</a> <a target="_blank" href="https://www.molaid.com/MS_712" class="compound-item" title="鸟苷 5'-磷酰-2-甲基咪唑">鸟苷 5'-磷酰-2-甲基咪唑</a> </div> </div> <div class="module" id="xiangguanjiegoufenlei"> <h3 class="module-title"><i class="iconfont icon-xiangguanjiegoufenlei"></i>相关结构分类</h3> <div class="compounds-list"> <a href="https://www.molaid.com/fenzi/10" class="compound-item" title="有机杂环化合物">有机杂环化合物</a> <a href="https://www.molaid.com/fenzi/11" class="compound-item" title="苯类化合物">苯类化合物</a> <a href="https://www.molaid.com/fenzi/12" class="compound-item" title="木脂素、新木脂素和相关化合物">木脂素、新木脂素和相关化合物</a> <a href="https://www.molaid.com/fenzi/13" class="compound-item" title="苯丙烷和聚酮">苯丙烷和聚酮</a> <a href="https://www.molaid.com/fenzi/14" class="compound-item" title="脂质和类脂质分子">脂质和类脂质分子</a> <a href="https://www.molaid.com/fenzi/15" class="compound-item" title="有机酸及其衍生物">有机酸及其衍生物</a> <a href="https://www.molaid.com/fenzi/16" class="compound-item" title="有机氧化合物">有机氧化合物</a> <a href="https://www.molaid.com/fenzi/17" class="compound-item" title="生物碱及其衍生物">生物碱及其衍生物</a> <a href="https://www.molaid.com/fenzi/18" class="compound-item" title="有机硫化合物">有机硫化合物</a> <a href="https://www.molaid.com/fenzi/19" class="compound-item" title="核苷、核苷酸和类似物">核苷、核苷酸和类似物</a> <a href="https://www.molaid.com/fenzi/20" class="compound-item" title="碳氢化合物衍生物">碳氢化合物衍生物</a> <a href="https://www.molaid.com/fenzi/21" class="compound-item" title="有机氮化合物">有机氮化合物</a> <a href="https://www.molaid.com/fenzi/22" class="compound-item" title="碳氢化合物">碳氢化合物</a> <a href="https://www.molaid.com/fenzi/23" class="compound-item" title="有机卤素化合物">有机卤素化合物</a> <a href="https://www.molaid.com/fenzi/24" class="compound-item" title="有机聚合物">有机聚合物</a> <a href="https://www.molaid.com/fenzi/25" class="compound-item" title="有机金属化合物">有机金属化合物</a> <a href="https://www.molaid.com/fenzi/26" class="compound-item" title="乙炔化物 ">乙炔化物 </a> <a href="https://www.molaid.com/fenzi/27" class="compound-item" title="有机磷化合物">有机磷化合物</a> <a href="https://www.molaid.com/fenzi/28" class="compound-item" title="叠烯">叠烯</a> <a href="https://www.molaid.com/fenzi/29" class="compound-item" title="有机1,3-偶极化合物">有机1,3-偶极化合物</a> <a href="https://www.molaid.com/fenzi/30" class="compound-item" title="碳化物">碳化物</a> <a href="https://www.molaid.com/fenzi/31" class="compound-item" title="有机盐">有机盐</a> <a href="https://www.molaid.com/fenzi/32" class="compound-item" title="有机阳离子">有机阳离子</a> <a href="https://www.molaid.com/fenzi/33" class="compound-item" title="卡宾">卡宾</a> <a href="https://www.molaid.com/fenzi/34" class="compound-item" title="有机阴离子">有机阴离子</a> </div> </div> </div> <div class="right"> <div class="module"> <link rel="stylesheet" href="https://www.molaid.com/assets/css/common/hot-molecular.css?v=202504271"> <div class="component-card hot-molecular-card" style="--color: #FF4539;"> <div class="title"> <h3 class="title-name">热门分子</h3> </div> <div class="card-content"> <ul class="list"> <li class="item item-special" data-sort="TOP"> <div class="item-img"> <img src="data:image/svg+xml;base64,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" alt=""> </div> <div class="card-info"> <div class="tag">TOP</div> <div class="name"><a target="_blank" href="https://www.molaid.com/MS_51724" title="喹啉 | 91-22-5">喹啉 | 91-22-5</a></div> </div> </li> <li class="item"><a target="_blank" href="https://www.molaid.com/MS_34489" title="水杨醛 | 90-02-8">水杨醛 | 90-02-8</a></li> <li class="item"><a target="_blank" href="https://www.molaid.com/MS_67661" title="二溴甲烷 | 74-95-3">二溴甲烷 | 74-95-3</a></li> <li class="item"><a target="_blank" href="https://www.molaid.com/MS_7911" title="谷胱甘肽 | 70-18-8">谷胱甘肽 | 70-18-8</a></li> <li class="item"><a target="_blank" href="https://www.molaid.com/MS_123893" title="L-乳酸 | 79-33-4">L-乳酸 | 79-33-4</a></li> <li class="item"><a target="_blank" href="https://www.molaid.com/MS_12646" title="苯巴比妥 | 50-06-6">苯巴比妥 | 50-06-6</a></li> <li class="item"><a target="_blank" href="https://www.molaid.com/MS_7140" title="辣椒碱 | 404-86-4">辣椒碱 | 404-86-4</a></li> <li class="item"><a target="_blank" href="https://www.molaid.com/MS_2086" title="非那明 | 300-62-9">非那明 | 300-62-9</a></li> <li class="item"><a target="_blank" href="https://www.molaid.com/MS_23762" title="百草枯 | 4685-14-7">百草枯 | 4685-14-7</a></li> <li class="item"><a target="_blank" href="https://www.molaid.com/MS_17154" title="联苯烯 | 259-79-0">联苯烯 | 259-79-0</a></li> <li class="item"><a target="_blank" href="https://www.molaid.com/MS_1288" title="香茅醛 | 106-23-0">香茅醛 | 106-23-0</a></li> <li class="item"><a target="_blank" href="https://www.molaid.com/MS_11726" title="苯甲腈 | 100-47-0">苯甲腈 | 100-47-0</a></li> <li class="item"><a target="_blank" href="https://www.molaid.com/MS_183591" title="4-硝基苯肼 | 100-16-3">4-硝基苯肼 | 100-16-3</a></li> <li class="item"><a target="_blank" href="https://www.molaid.com/MS_478" title="黄夹苷 | 11018-93-2">黄夹苷 | 11018-93-2</a></li> </ul> </div> </div> </div> </div> </div> <div class="data-change m"> <div class="page-turn"> <div class="page-turn-item prev"> <a target="_blank" href="https://www.molaid.com/MS_741417">上一个:3,4-bis(4-(2-(diethylamino)ethoxy)phenyl)-2H-chromen-2-one</a> </div> <div class="page-turn-item next"> <a target="_blank" href="https://www.molaid.com/MS_741419">下一个:5-chloro-4-nitrobenzene-1,3-diol</a> </div> </div> </div> </div> </div> <div id="intsynth-footer"> <link rel="stylesheet" href="https://www.molaid.com/assets/css/common/footer.css?v=202504271"> <div class="footer"> <div class="footer-container m"> <div class="footer-item"> <div class="title">支持</div> <div class="product-list"> <div class="product-item"> <a href="https://rxn.molaid.com/introduction" target="_blank" rel="nofollow">产品介绍</a> </div><div class="product-item"> <a href="https://rxn.molaid.com/pricing" target="_blank" rel="nofollow">定价</a> </div> <div class="product-item"> <a href="https://chem.molaid.com/material/list?source=UserSourcePortal" target="_blank" rel="nofollow">数据库</a> </div> </div> </div> <div class="footer-item"> <div class="title">联系我们</div> <div class="product-list"> <div class="product-item flex"> <img class="item-icon" src="/assets/images/common/phone.svg" alt=""><div> <a href="tel:14702887347">14702887347</a>,<a href="tel:18328613625">18328613625</a> </div> </div> <div class="product-item flex"> <img class="item-icon" src="/assets/images/common/email.svg" alt=""> <a href="mailto:service@tanqingsk.com">service@tanqingsk.com</a> </div> <div class="product-item flex"> <img class="item-icon" src="/assets/images/common/position.svg" alt=""> <div>成都市高新区孵化园9F505</div> </div> </div> </div> <div class="footer-item"> <div class="title">关注我们</div> <div class="wechat flex"> <div class="wechat-type flex1"> <img class="wechat-icon" src="/assets/images/common/wechat.svg" alt=""> <p class="wechat-type-text">公众号</p> </div> <div class="qrcode-container"> <img src="/assets/images/common/qrcode-wx-official.jpg" alt="" class="qrcode"> </div> </div> </div> </div> <footer class="footer-bottom"> <span>© molaid.com 2024 碳氢数科(成都)信息技术有限公司 All Rights Reserved.</span><span>  </span><a href="https://beian.miit.gov.cn" target="_blank" rel="nofollow">蜀ICP备2024049375号-4</a> </footer> </div> </div> <!-- 公共组件 --> <div class="return-top" onclick="returnToTop()"></div> <div class="cover-tips"> <div class="img"></div> <p class="text"></p> </div> <div class="big-img"> <div class="big-img-content"></div> </div> </div> <!-- 全局组件的js --> <script type="text/javascript" src="https://www.molaid.com/assets/js/common/request/index.js?v=202504271"></script> <script !src=""> var _hmt = _hmt || []; (function() { var hm = document.createElement("script"); hm.src = "https://hm.baidu.com/hm.js?507a154709a3ee985b6b82c9f625abbc"; var s = document.getElementsByTagName("script")[0]; s.parentNode.insertBefore(hm, s); })(); </script> <script type="text/javascript" src="https://www.molaid.com/assets/js/web/compounds/detail.js?v=202504271"></script> </body> </html>