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β-Cyclohexen-(2)-acrylsaeure | 90534-29-5

中文名称
——
中文别名
——
英文名称
β-Cyclohexen-(2)-acrylsaeure
英文别名
3-Cyclohex-2-en-1-ylprop-2-enoic acid;3-cyclohex-2-en-1-ylprop-2-enoic acid
β-Cyclohexen-(2)-acrylsaeure化学式
CAS
90534-29-5
化学式
C9H12O2
mdl
——
分子量
152.193
InChiKey
OPWKXYVUJOOERX-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

  • 沸点:
    284.9±29.0 °C(Predicted)
  • 密度:
    1.168±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.2
  • 重原子数:
    11
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    37.3
  • 氢给体数:
    1
  • 氢受体数:
    2

文献信息

  • [EN] METHOD FOR PRODUCING -MERCAPTO CARBOXYLIC ACIDS<br/>[FR] PROCÉDÉ D'ÉLABORATION D'ACIDES BÊTA-MERCAPTO CARBOXYLIQUES
    申请人:SHOWA DENKO KK
    公开号:WO2009113711A1
    公开(公告)日:2009-09-17
    An object of the present invention is to provide a method for industrially producing beta-mercapto carboxylic acids that are useful as synthetic raw materials for medicines and agrochemicals or as additives for polymer compounds from easily available alpha,beta-unsaturated carboxylic acids in high yields and productivity. The present invention is characterized in that a solvent having an amide group and represented by the formula (1) is used when the alpha,beta-unsaturated carboxylic acids are reacted with hydrogen sulfides to produce the beta-mercapto carboxylic acids. Particularly, it is more preferable to carry out the reaction at a pH range of 6.0 to 8.5: (In the formula (1), R1 represents any one of a hydrogen atom, an alkoxy group having 1 to 5 carbon atoms, an alkyl group having 1 to 5 carbon atoms, an amino group, and an alkylamino group having 1 to 5 carbon atoms; R2 and R3 each represents independently any one of a hydrogen atom and an alkyl group having 1 to 5 carbon atoms; when both R2 and R3 are not a hydrogen atom, R2 and R3 may together form a ring structure through an alkylene group; and when both R1 and R2 are not a hydrogen atom, R1 and R2 may form a ring structure through an alkylene group).
    本发明的目的是提供一种工业生产β-巯基羧酸的方法,该方法可以从易得到的α,β-不饱和羧酸高产高效地合成用于药品和农药的合成原料或聚合物化合物的添加剂。本发明的特点在于,在α,β-不饱和羧酸与氢硫化物反应产生β-巯基羧酸时,使用具有酰胺基的溶剂,该溶剂由公式(1)表示。特别是,在pH范围为6.0至8.5的条件下进行反应更为理想:(在公式(1)中,R1代表氢原子、具有1至5个碳原子的烷氧基、具有1至5个碳原子的烷基、氨基和具有1至5个碳原子的烷基氨基中的任意一种;R2和R3各自独立地代表氢原子和具有1至5个碳原子的烷基中的任意一种;当R2和R3均不是氢原子时,R2和R3可以通过烷基链结构形成环状结构;当R1和R2均不是氢原子时,R1和R2可以通过烷基链结构形成环状结构。)
  • METHOD FOR PRODUCING BETA-MERCAPTO CARBOXYLIC ACIDS
    申请人:Showa Denko K.K.
    公开号:EP2268614B1
    公开(公告)日:2013-05-15
  • METHOD FOR PRODUCING BETA-MERCAPTO CARBOXYLIC ACIDS
    申请人:Aoki Hidemasa
    公开号:US20110015436A1
    公开(公告)日:2011-01-20
    An object of the present invention is to provide a method for industrially producing β-mercapto carboxylic acids that are useful as synthetic raw materials for medicines and agrochemicals or as additives for polymer compounds from easily available α,β-unsaturated carboxylic acids in high yields and productivity. The present invention is characterized in that a solvent having an amide group and represented by the formula (1) is used when the α,β-unsaturated carboxylic acids are reacted with hydrogen sulfides to produce the β-mercapto carboxylic acids. Particularly, it is more preferable to carry out the reaction at a pH range of 6.0 to 8.5: (In the formula (1), R 1 represents any one of a hydrogen atom, an alkoxy group having 1 to 5 carbon atoms, an alkyl group having 1 to 5 carbon atoms, an amino group, and an alkylamino group having 1 to 5 carbon atoms; R 2 and R 3 each represents independently any one of a hydrogen atom and an alkyl group having 1 to 5 carbon atoms; when both R 2 and R 3 are not a hydrogen atom, R 2 and R 3 may together form a ring structure through an alkylene group; and when both R 1 and R 2 are not a hydrogen atom, R 1 and R 2 may form a ring structure through an alkylene group).
  • US8258340B2
    申请人:——
    公开号:US8258340B2
    公开(公告)日:2012-09-04
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