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3-苯甲酰基-6-溴色烯-2-酮 | 2199-85-1

中文名称
3-苯甲酰基-6-溴色烯-2-酮
中文别名
——
英文名称
3-benzoyl-6-bromo-2H-chromen-2-one
英文别名
3-benzoyl-6-bromochromen-2-one;6-bromo-3-benzoyl coumarin
3-苯甲酰基-6-溴色烯-2-酮化学式
CAS
2199-85-1
化学式
C16H9BrO3
mdl
——
分子量
329.15
InChiKey
OXSWLSMWLZZECK-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):
    4.2
  • 重原子数:
    20
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    43.4
  • 氢给体数:
    0
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2932209090

SDS

SDS:256e3ed582cbf88d025aaf9885b3e24a
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反应信息

  • 作为反应物:
    描述:
    3-苯甲酰基-6-溴色烯-2-酮哌啶 作用下, 以 乙醇 为溶剂, 生成 1,3-diamino-11-bromo-7-oxo-6-phenyl-7,12b-dihydrochromeno[4',3':4,5]pyrano[2,3-b]pyridine-2-carbonitrile
    参考文献:
    名称:
    一些具有预期生物活性的新香豆素杂种的高效合成
    摘要:
    DOI:
    10.3987/com-20-14300
  • 作为产物:
    描述:
    苯甲酰乙酸乙酯5-溴水杨醛L-脯氨酸 作用下, 反应 0.58h, 以88%的产率得到3-苯甲酰基-6-溴色烯-2-酮
    参考文献:
    名称:
    Synthesis of 3-substituted Coumarins: An Efficient Green Approach Using L-proline as Catalyst in Triethanolamine Medium
    摘要:
    在绿色条件下,采用 Knoevenagel 方法从水杨醛 1 和活性亚甲基化合物 2 非常高效地合成了 3-取代香豆素。研究了催化剂和溶剂对这种缩合反应的影响。结果发现,L-脯氨酸是该反应的最佳催化剂,三乙醇胺是最佳反应介质。
    DOI:
    10.2174/1570178611666140512215136
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文献信息

  • SILANE COUPLING COMPOUNDS AND MEDICAL AND/OR DENTAL CURABLE COMPOSITIONS COMPRISING THE SAME
    申请人:KABUSHIKI KAISHA SHOFU
    公开号:US20190300552A1
    公开(公告)日:2019-10-03
    The present invention relate to a novel silane coupling agent and a medical and/or dental curable composition comprising the same. It is an object of the present invention to provide a novel silane coupling agent that imparts high affinity to a radical polymerizable monomer, thereby imparting high mechanical strength, flexibility and durability when used for a medical and/or dental curable composition, and an inorganic filler surface-treated with the novel silane coupling agent and a novel medical and/or dental curable composition. A silane coupling agent including repeating units such as a urethane bond and polyethylene glycol (ether bond) at a specific position is used.
    本发明涉及一种新型硅烷偶联剂以及包括该偶联剂的医用和/或牙科可固化组合物。本发明的目的是提供一种新型硅烷偶联剂,使其对自由基聚合单体具有高亲和力,从而在用于医用和/或牙科可固化组合物时赋予高机械强度、柔韧性和耐久性,并且包括经新型硅烷偶联剂表面处理的无机填料和新型医用和/或牙科可固化组合物。该硅烷偶联剂包括在特定位置具有尿素键和聚乙二醇(醚键)等重复单元。
  • Synthesis and selective human monoamine oxidase inhibition of 3-carbonyl, 3-acyl, and 3-carboxyhydrazido coumarin derivatives
    作者:Daniela Secci、Simone Carradori、Adriana Bolasco、Paola Chimenti、Matilde Yáñez、Francesco Ortuso、Stefano Alcaro
    DOI:10.1016/j.ejmech.2011.07.017
    日期:2011.10
    Several 3-carbonyl (1–26), 3-acyl (27–52), and 3-carboxyhydrazido (53–58) coumarins have been synthesized in high yields (72–99%) and tested in vitro for their human monoamine oxidase A and B (hMAO-A and hMAO-B) inhibitory activity. Different substituents on the coumarin nucleus were evaluated for their effect on biological activity and isoform selectivity. Substitution at position C7 of the 3-ethyl
    几个-3-羰基(1 - 26),3-酰基(27 - 52),和3- carboxyhydrazido(53 - 58)香豆素已经以高收率(72-99%)合成并测试在体外对它们的人类单胺氧化酶A和B(hMAO-A和hMAO-B)的抑制活性。评价了香豆素核上的不同取代基对生物活性和同工型选择性的影响。对于使用IC 50获得高效且选择性的hMAO-B抑制剂而言,在3-乙酯香豆素环的C7位取代或在C3引入肼基取代基很重要。值在纳摩尔范围内。一些衍生物也进行了稳定性测试,在体外没有化​​学裂解。
  • α-Glucosidase inhibitory antihyperglycemic activity of substituted chromenone derivatives
    作者:B. China Raju、Ashok K. Tiwari、J. Ashok Kumar、A. Zehra Ali、Sachin B. Agawane、G. Saidachary、K. Madhusudana
    DOI:10.1016/j.bmc.2009.10.047
    日期:2010.1
    varying degrees of α-glucosidase inhibitory and DPPH scavenging activity. Compound 4x emerged as the most potent α-glucosidase inhibitor in present series of compounds owing to the presence of 3-acetyl-6-(6-methoxy-3-pyridyl) group on chromenone; however, it could not display DPPH scavenging activity and was found to be mixed non-competitive type inhibitor of rat intestinal α-glucosidase. When tested in
    采用各种合成策略(包括Pechmann缩合,Knoevenagel缩合,Reimer-Tiemann反应和Suzuki偶联)以很高的收率合成了包括新的chromenone衍生物在内的3,4-和3,6-二取代的chromenones系列。筛选了合成的化合物(4a – z)的体外α-葡萄糖苷酶抑制作用和1,1-二苯基-2-吡啶并肼基(DPPH)自由基清除活性。大多数化合物表现出不同程度的α-葡萄糖苷酶抑制和DPPH清除活性。复合4倍由于在色酮上存在3-乙酰基-6-(6-甲氧基-3-吡啶基)基团,在本系列化合物中成为最有效的α-葡萄糖苷酶抑制剂。然而,它不能表现出DPPH清除活性,并且被发现是大鼠肠内α-葡萄糖苷酶的非竞争性混合型抑制剂。当在体内测试淀粉负载的Wistar大鼠的降血糖活性时,它显示出显着的降血糖特性。这是首次将大鼠肠道α-葡萄糖苷酶抑制特性归为此类新的色农酮,并提出了具有α-葡萄
  • DENTAL ADHESIVE
    申请人:KURARAY NORITAKE DENTAL INC.
    公开号:US20170196778A1
    公开(公告)日:2017-07-13
    The present invention provides a dental adhesive exhibiting excellent initial bond strength and bond durability to both enamel and dentin. The present invention relates to a dental adhesive containing: an asymmetric acrylamide-methacrylic acid ester compound (a); an acid group-containing (meth)acrylic polymerizable monomer (b); and a water-soluble polymerizable monomer (c). The asymmetric acrylamide-methacrylic acid ester compound (a) is represented by the following general formula (1): where X is an optionally substituted, linear or branched C 1 to C 6 aliphatic group or an optionally substituted aromatic group, the aliphatic group is optionally interrupted by at least one linking group selected from the group consisting of —O—, —S—, —CO—, —CO—O—, —O—CO—, —NR 1 —, —CO—NR 1 —, —NR 1 —CO—, —CO—O—NR 1 —, —O—CO—NR 1 —, and —NR 1 —CO—NR 1 —, and R 1 is a hydrogen atom or an optionally substituted, linear or branched C 1 to C 6 aliphatic group.
    本发明提供了一种牙科粘接剂,具有优异的初始粘接强度和对牙釉质和牙本质的粘接耐久性。本发明涉及一种含有以下成分的牙科粘接剂:不对称丙烯酰胺-甲基丙烯酸酯化合物(a);含酸基的(甲基)丙烯酸聚合单体(b);以及水溶性聚合单体(c)。不对称丙烯酰胺-甲基丙烯酸酯化合物(a)由下述一般式(1)表示:其中X是可选择取代的线性或支链状的C1到C6脂肪族基或可选择取代的芳香族基,所述脂肪族基可被来自由—O—、—S—、—CO—、—CO—O—、—O—CO—、—NR1—、—CO—NR1—、—NR1—CO—、—CO—O—NR1—、—O—CO—NR1—和—NR1—CO—NR1—组成的至少一个连接基中断,R1为氢原子或可选择取代的线性或支链状的C1到C6脂肪族基。
  • SELF-ADHESIVE DENTAL COMPOSITE RESIN
    申请人:KURARAY NORITAKE DENTAL INC.
    公开号:US20170135910A1
    公开(公告)日:2017-05-18
    The present invention provides a self-adhesive composite resin having excellent adhesiveness to tooth structures and excellent mechanical strength. The present invention relates to a self-adhesive dental composite resin containing: an asymmetric acrylamide-methacrylic acid ester compound (a); an acid group-containing (meth)acrylic polymerizable monomer (b); a hydrophobic crosslinkable polymerizable monomer (c); a photopolymerization initiator (d); and a filler (e). The asymmetric acrylamide-methacrylic acid ester compound (a) is represented by the following general formula (1): where X is an optionally substituted, linear or branched C 1 to C 6 aliphatic group or an optionally substituted aromatic group, the aliphatic group is optionally interrupted by at least one linking group selected from the group consisting of —O—, —S—, —CO—, —CO—O—, —O—CO—, —NR 1 —, —CO—NR 1 —, —NR 1 —CO—, —CO—O—NR 1 —, —O—CO—NR 1 —, and —NR 1 —CO—NR 1 —, and R 1 is a hydrogen atom or an optionally substituted, linear or branched C 1 to C 6 aliphatic group.
    本发明提供了一种具有优异粘附性和优异机械强度的自粘合复合树脂。本发明涉及一种自粘合牙科复合树脂,包含:不对称的丙烯酰胺-甲基丙烯酸酯化合物(a);含酸基的(甲基)丙烯酸聚合单体(b);疏水性交联聚合单体(c);光聚合引发剂(d);和填料(e)。不对称的丙烯酰胺-甲基丙烯酸酯化合物(a)由以下通式(1)表示:其中X是可选取代的线性或支链的C1至C6脂肪族基团或可选取代的芳香族基团,脂肪族基团可由以下组成的至少一种连接基团中断:—O—、—S—、—CO—、—CO—O—、—O—CO—、—NR1—、—CO—NR1—、—NR1—CO—、—CO—O—NR1—、—O—CO—NR1—和—NR1—CO—NR1—,R1为氢原子或可选取代的线性或支链的C1至C6脂肪族基团。
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