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4-(三甲基硅基乙炔基)苄基甲醇 | 275386-60-2

中文名称
4-(三甲基硅基乙炔基)苄基甲醇
中文别名
4-(三甲基甲硅烷基乙炔)苄醇;4-(三甲基硅基乙炔基)苄醇
英文名称
(4-((trimethylsilyl)ethynyl)phenyl)methanol
英文别名
4-(trimethylsilylethynyl)benzyl alcohol;[4-(2-trimethylsilylethynyl)phenyl]methanol
4-(三甲基硅基乙炔基)苄基甲醇化学式
CAS
275386-60-2
化学式
C12H16OSi
mdl
MFCD08457640
分子量
204.344
InChiKey
WBNXRSFSSANBSA-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

物化性质

  • 熔点:
    68-72 °C
  • 沸点:
    274.6±32.0 °C(Predicted)
  • 密度:
    0.99±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.21
  • 重原子数:
    14
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.333
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    1

安全信息

  • 海关编码:
    2931900090
  • WGK Germany:
    3
  • 危险性防范说明:
    P280,P305+P351+P338
  • 危险性描述:
    H302
  • 储存条件:
    2-8°C,存放在干燥密封的环境中。

SDS

SDS:91fd50a32120ec5003a91ef5dc247500
查看

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    4-(三甲基硅基乙炔基)苄基甲醇咪唑甲醇正丁基锂 、 palladium 10% on activated carbon 、 四丁基氟化铵氢气potassium carbonate三乙胺 、 sodium iodide 、 sodium hydroxide 作用下, 以 四氢呋喃正己烷二氯甲烷乙酸乙酯N,N-二甲基甲酰胺丙酮 为溶剂, -78.0~20.0 ℃ 、2.0 MPa 条件下, 反应 25.08h, 生成 4-丙基苯乙酸
    参考文献:
    名称:
    EP2610243
    摘要:
    公开号:
  • 作为产物:
    描述:
    4-三甲基硅乙炔基苯甲醛 在 lithium aluminium tetrahydride 作用下, 以 四氢呋喃 为溶剂, 反应 4.0h, 以83%的产率得到4-(三甲基硅基乙炔基)苄基甲醇
    参考文献:
    名称:
    Thermoresponsive Helical Poly(phenylacetylene)s
    摘要:
    Poly(phenylacetylene) (PPA) bearing dendritic oligo(ethylene glycol) (OEG) as pendants was synthesized, and its thermoresponsiveness and helical conformation were investigated. Despite the steric hindrance of the bulky pendants in the homopolymer PPA-OEG, the chirality could be efficiently transferred from pendant alanine moieties to PPA main chain through ester linkage. In order to examine the steric effect of pendants on chiral transformation, a model PPA homopolymer PPA-Boc which carries less bulky moieties was prepared for comparison. The chiroptical properties of these thermoresponsive PPAs were further investigated by varying temperature to examine the effects of their thermoresponsiveness. In addition, PPA copolymers PPA-BDY bearing OEG dendron and fluorescent boradiazaindacene (BDY) chromophore showed excellent thermoresponsive properties and interesting fluorescence enhancement at elevated temperatures. To investigate the rigidity effects of polymer backbone on the thermally induced fluorescence enhancement, a nonchiral polymer carrying the same pendants but with polymethacrylate as the backbone (PMA-OEG) was prepared. It was found that the chiroptical and fluorescence properties of these PPAs are dependent not only on their chemical structures but also on the thermoresponsiveness.
    DOI:
    10.1021/ma5003529
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文献信息

  • Redox-Selective Generation of Aldehydes and H<sub>2</sub>from Alcohols under Visible Light
    作者:Zijun Liu、Joaquim Caner、Akihiko Kudo、Hiroshi Naka、Susumu Saito
    DOI:10.1002/chem.201301347
    日期:2013.7.15
    Photosynthetic dehydrogenation: Potential usefulness of visiblelight‐induced dehydrogenation of alcohols in organic synthesis was demonstrated, in which aldehydes and H2 were afforded by using Ru/SrTiO3:Rh and water (see scheme). Water was essential for the reaction. High efficiency (TON: up to 15 400 based on Rh; H2 and aldehyde evenly generated) and high selectivity were achieved.
    光合脱氢:证明了可见光诱导的醇在有机合成中的潜在用途,其中通过使用Ru / SrTiO 3:Rh和水提供醛和H 2(请参见方案)。水对于反应是必不可少的。获得了高效率(TON:基于Rh最高可达15400; H 2和醛均匀生成)和高选择性。
  • Synthesis of siRNAs incorporated with cationic peptides R8G7 and R8A7 and the effect of the modifications on siRNA properties
    作者:Miho Matsubara、Kenji Honda、Koki Ozaki、Ryohei Kajino、Yuri Kakisawa、Yusuke Maeda、Yoshihito Ueno
    DOI:10.1039/d0ra05919f
    日期:——
    that R8G7 and R8A7 modifications increased the thermal stability of the siRNA duplexes. Incorporating these peptides at the 3′-ends of the siRNA passenger strands increased the stability of the siRNAs in a buffer containing bovine serum. Further, we found that the peptide–siRNA conjugates did not show sufficient RNA interference (RNAi) activity in the absence of the transfection reagent; however, when
    小干扰 RNA (siRNA) 可用作创新的下一代药物。然而,在 siRNA 的治疗应用中存在一些挑战,包括它们的低细胞膜通透性。在本研究中,我们设计并合成了 siRNA,并结合阳离子肽 R8G7 和 R8A7 来提高 siRNA 的细胞膜通透性。热变性研究表明,R8G7 和 R8A7 修饰增加了 siRNA 双链体的热稳定性。在 siRNA 过客链的 3' 末端掺入这些肽可提高 siRNA 在含有牛血清的缓冲液中的稳定性。此外,我们发现在没有转染试剂的情况下,肽-siRNA 偶联物没有表现出足够的 RNA 干扰 (RNAi) 活性。然而,当使用转染试剂时,
  • Iron‐Catalyzed Tertiary Alkylation of Terminal Alkynes with 1,3‐Diesters via a Functionalized Alkyl Radical
    作者:Ming‐Qing Tian、Zhen‐Yao Shen、Xuefei Zhao、Patrick J. Walsh、Xu‐Hong Hu
    DOI:10.1002/anie.202100641
    日期:2021.4.19
    Direct oxidative C(sp)−H/C(sp3)−H crosscoupling offers an ideal and environmentally benign protocol for C(sp)−C(sp3) bond formations. As such, reactivity and site‐selectivity with respect to C(sp3)−H bond cleavage have remained a persistent challenge. Herein is reported a simple method for ironcatalyzed/silver‐mediated tertiary alkylation of terminal alkynes with readily available and versatile 1
    直接氧化的C(sp)-H / C(sp 3)-H交叉偶联为C(sp)-C(sp 3)键的形成提供了理想的环境友好方案。因此,相对于C(sp 3)-H键裂解的反应性和位点选择性仍然是一个持续的挑战。本文报道了一种简便易行的方法,可利用易于获得的通用1,3-二羰基化合物对末端炔烃进行铁催化/银介导的叔烷基化。该反应适用于多种底物,即使使用含有其他叔,苄基和C(sp 3)-H将α键合至杂原子。对产品的精心设计使得可以合成一系列通用的构建基块。对照实验暗示了以碳为中心的第三级自由基物种的原位生成。
  • [EN] APOPTOSIS INHIBITORS<br/>[FR] INHIBITEURS DE L'APOPTOSE
    申请人:NAT INSTITUTE OF BIOLOGICAL SCIENCES BEIJING
    公开号:WO2018014802A1
    公开(公告)日:2018-01-25
    The invention provides compounds that are inhibitors or covalent modifiers of succinate dehydrogenase subunit B (SDHB) and/or inhibitors of apoptosis, and pharmaceutically acceptable salts, hydrides and stereoisomers thereof. The compounds are employed in pharmaceutical compositions, and methods of making and use, including treating a person in need thereof with an effective amount of the compound or composition.
    这项发明提供了一种抑制琥珀酸脱氢酶亚基B(SDHB)或共价修饰剂的化合物,以及抑制凋亡的化合物,以及这些化合物的药用盐、氢化物和立体异构体。这些化合物用于制备药物组合物,以及制备和使用方法,包括使用有效量的化合物或组合物治疗需要的人。
  • Synthesis and Biological Evaluation of PF-543 Derivative
    作者:Seon Woong Kim、Taeho Lee、Joo-Youn Lee、Sanghee Kim、Hee-Sook Jun、Eun-Young Park、Dong Jae Baek
    DOI:10.2174/1570178615666181009121430
    日期:2018.12.4
    <p>PF-543 has been known as a substance that strongly inhibits SK1. However, it also exhibits antineoplastic activity that is lower than other inhibitors of SK1. In this study, we compared PF-543 and synthesized a newly designed derivative of PF-543 (compound 2) in which two aromatic structures were connected in para-form. The synthesized derivative showed inhibitory effect on SK1, similar to that of PF-543. However, it was more cytotoxic to HT29, AGS, and PC3 cells than PF-543. We also carried out a docking study for SK1 and demonstrated that the synthesized derivative showed interaction with SK1 similar to PF-543. Results obtained from this study suggest that the structure of compound 2 may be well substituted for the structure of PF-543 in terms of biological activity, providing us important structural information for the design of new derivatives of PF-543.</p></sec></div> <div class="value-text ch">PF-543被认为是一种强烈抑制SK1的物质。然而,它也表现出比其他SK1抑制剂更低的抗肿瘤活性。在这项研究中,我们比较了PF-543并合成了一种新设计的PF-543衍生物(化合物2),其中两个芳香结构连接在对位。合成的衍生物显示出对SK1的抑制作用,类似于PF-543。然而,它对HT29、AGS和PC3细胞的细胞毒性比PF-543更强。我们还对SK1进行了对接研究,并证明合成的衍生物与PF-543类似地与SK1发生相互作用。本研究得到的结果表明,化合物2的结构在生物活性方面可能很好地替代PF-543的结构,为设计新的PF-543衍生物提供了重要的结构信息。</div> </div> </li> </ul> <a href="https://chem.molaid.com/material/detail?source=UserSourcePortal&id=3101928y7c5af12149N0&inchikey=WBNXRSFSSANBSA-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_9" class="compound-item" title="(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇">(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇</a> <a target="_blank" href="https://www.molaid.com/MS_22" class="compound-item" title="(S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚">(S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚</a> <a target="_blank" href="https://www.molaid.com/MS_30" class="compound-item" title="(S)-盐酸沙丁胺醇">(S)-盐酸沙丁胺醇</a> <a target="_blank" href="https://www.molaid.com/MS_38" class="compound-item" title="(S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯">(S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯</a> <a target="_blank" href="https://www.molaid.com/MS_44" class="compound-item" title="(S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯">(S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯</a> <a target="_blank" href="https://www.molaid.com/MS_47" class="compound-item" title="(S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲">(S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲</a> <a target="_blank" href="https://www.molaid.com/MS_50" class="compound-item" title="(R)富马酸托特罗定">(R)富马酸托特罗定</a> <a target="_blank" href="https://www.molaid.com/MS_51" class="compound-item" title="(R)-(-)-盐酸尼古地平">(R)-(-)-盐酸尼古地平</a> <a target="_blank" href="https://www.molaid.com/MS_52" class="compound-item" title="(R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满">(R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满</a> <a target="_blank" href="https://www.molaid.com/MS_63" class="compound-item" title="(R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯">(R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯</a> <a target="_blank" href="https://www.molaid.com/MS_71" class="compound-item" title="(R)-2-[((二苯基膦基)甲基]吡咯烷">(R)-2-[((二苯基膦基)甲基]吡咯烷</a> <a target="_blank" href="https://www.molaid.com/MS_77" class="compound-item" title="(N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺)">(N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺)</a> <a target="_blank" href="https://www.molaid.com/MS_102" class="compound-item" title="(5-溴-2-羟基苯基)-4-氯苯甲酮">(5-溴-2-羟基苯基)-4-氯苯甲酮</a> <a target="_blank" href="https://www.molaid.com/MS_103" class="compound-item" title="(5-溴-2-氯苯基)(4-羟基苯基)甲酮">(5-溴-2-氯苯基)(4-羟基苯基)甲酮</a> <a target="_blank" href="https://www.molaid.com/MS_107" class="compound-item" title="(5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓)">(5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓)</a> <a target="_blank" href="https://www.molaid.com/MS_111" class="compound-item" title="(4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯">(4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯</a> <a target="_blank" href="https://www.molaid.com/MS_123" class="compound-item" title="(4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮">(4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮</a> <a target="_blank" href="https://www.molaid.com/MS_125" class="compound-item" 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title="(2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺">(2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺</a> <a target="_blank" href="https://www.molaid.com/MS_163" class="compound-item" title="(2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺">(2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺</a> <a target="_blank" href="https://www.molaid.com/MS_180" class="compound-item" title="(2-硝基苯基)磷酸三酰胺">(2-硝基苯基)磷酸三酰胺</a> <a target="_blank" href="https://www.molaid.com/MS_187" class="compound-item" title="(2,6-二氯苯基)乙酰氯">(2,6-二氯苯基)乙酰氯</a> <a target="_blank" href="https://www.molaid.com/MS_189" class="compound-item" title="(2,3-二甲氧基-5-甲基苯基)硼酸">(2,3-二甲氧基-5-甲基苯基)硼酸</a> <a target="_blank" href="https://www.molaid.com/MS_195" class="compound-item" title="(1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇">(1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇</a> <a target="_blank" href="https://www.molaid.com/MS_207" class="compound-item" title="(1-(4-氟苯基)环丙基)甲胺盐酸盐">(1-(4-氟苯基)环丙基)甲胺盐酸盐</a> <a target="_blank" href="https://www.molaid.com/MS_208" class="compound-item" title="(1-(3-溴苯基)环丁基)甲胺盐酸盐">(1-(3-溴苯基)环丁基)甲胺盐酸盐</a> <a target="_blank" href="https://www.molaid.com/MS_209" class="compound-item" title="(1-(2-氯苯基)环丁基)甲胺盐酸盐">(1-(2-氯苯基)环丁基)甲胺盐酸盐</a> <a target="_blank" href="https://www.molaid.com/MS_210" class="compound-item" title="(1-(2-氟苯基)环丙基)甲胺盐酸盐">(1-(2-氟苯基)环丙基)甲胺盐酸盐</a> <a target="_blank" href="https://www.molaid.com/MS_213" class="compound-item" title="(-)-去甲基西布曲明">(-)-去甲基西布曲明</a> <a target="_blank" href="https://www.molaid.com/MS_228" class="compound-item" title="龙胆酸钠">龙胆酸钠</a> <a target="_blank" href="https://www.molaid.com/MS_229" class="compound-item" title="龙胆酸叔丁酯">龙胆酸叔丁酯</a> <a target="_blank" href="https://www.molaid.com/MS_230" class="compound-item" title="龙胆酸">龙胆酸</a> <a target="_blank" href="https://www.molaid.com/MS_234" class="compound-item" title="龙胆紫">龙胆紫</a> <a target="_blank" href="https://www.molaid.com/MS_235" class="compound-item" title="龙胆紫">龙胆紫</a> <a target="_blank" href="https://www.molaid.com/MS_248" class="compound-item" title="齐达帕胺">齐达帕胺</a> <a target="_blank" href="https://www.molaid.com/MS_249" class="compound-item" title="齐诺康唑">齐诺康唑</a> <a target="_blank" href="https://www.molaid.com/MS_260" class="compound-item" title="齐洛呋胺">齐洛呋胺</a> <a target="_blank" href="https://www.molaid.com/MS_285" class="compound-item" title="齐墩果-12-烯[2,3-c][1,2,5]恶二唑-28-酸苯甲酯">齐墩果-12-烯[2,3-c][1,2,5]恶二唑-28-酸苯甲酯</a> <a target="_blank" href="https://www.molaid.com/MS_295" class="compound-item" title="齐培丙醇">齐培丙醇</a> <a target="_blank" href="https://www.molaid.com/MS_296" class="compound-item" title="齐咪苯">齐咪苯</a> <a target="_blank" href="https://www.molaid.com/MS_297" class="compound-item" title="齐仑太尔">齐仑太尔</a> <a target="_blank" href="https://www.molaid.com/MS_329" class="compound-item" title="黑染料">黑染料</a> <a target="_blank" href="https://www.molaid.com/MS_347" class="compound-item" title="黄酮,5-氨基-6-羟基-(5CI)">黄酮,5-氨基-6-羟基-(5CI)</a> <a target="_blank" href="https://www.molaid.com/MS_354" class="compound-item" title="黄酮,6-氨基-3-羟基-(6CI)">黄酮,6-氨基-3-羟基-(6CI)</a> <a target="_blank" href="https://www.molaid.com/MS_370" class="compound-item" title="黄蜡,合成物">黄蜡,合成物</a> <a target="_blank" href="https://www.molaid.com/MS_377" class="compound-item" title="黄草灵钾盐">黄草灵钾盐</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" 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