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

Adipinsaeuredithiophenylester | 41117-90-2

中文名称
——
中文别名
——
英文名称
Adipinsaeuredithiophenylester
英文别名
di-S-phenyl thioadipate;1,6-dithio-adipic acid S,S'-diphenyl ester;1,6-Dithio-adipinsaeure-S,S'-diphenylester;S~1~,S~6~-Diphenyl hexanebis(thioate);1-S,6-S-diphenyl hexanebis(thioate)
Adipinsaeuredithiophenylester化学式
CAS
41117-90-2
化学式
C18H18O2S2
mdl
——
分子量
330.472
InChiKey
VESNZOIGQGPYFP-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):
    4.8
  • 重原子数:
    22
  • 可旋转键数:
    9
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    84.7
  • 氢给体数:
    0
  • 氢受体数:
    4

SDS

SDS:386562beb55bd31a72e0bd07f1fd7b63
查看

反应信息

  • 作为产物:
    参考文献:
    名称:
    从羧酸和硫醇轻松合成羧酸硫醇酯
    摘要:
    通过硫醇与由游离羧酸和对甲苯磺酸2-氟-1-甲基吡啶鎓原位形成的酰氧基吡啶鎓盐反应,以良好的产率制备各种硫羟酸酯。
    DOI:
    10.1246/cl.1976.741
点击查看最新优质反应信息

文献信息

  • Method for Producing Carboxylic Acid Thioester
    申请人:Mitsubishi Chemical Corporation
    公开号:US20180265461A1
    公开(公告)日:2018-09-20
    According to the present invention, there is provided a method for producing carboxylic acid thioester, comprising reacting a compound represented by the following formula (I), carboxylic acid and thiol in the presence of a catalyst including at least one Group 2 metal compound. The production method is a production method which is simple in reaction operation, which places a small load on the environment and the human body and which enables carboxylic acid thioester to be catalytically obtained at a high yield even at a normal temperature and a normal pressure (25° C., 1 atm). In the formula (I), R 1 and R 2 each independently represent a hydrocarbon group having 1 to 20 carbon atoms.
    根据本发明,提供了一种生产羧酸酯的方法,包括在至少包括一种第2族属化合物的催化剂存在下,将下式(I)所代表的化合物、羧酸醇反应。该生产方法是一种在反应操作上简单、对环境和人体负荷小的生产方法,即使在常温和常压(25°C,1大气压)下也能以高产率催化获得羧酸酯。在式(I)中,R1和R2各自独立地表示具有1至20个碳原子的碳氢基团。
  • THE REACTION OF TRIMETHYLSILYL SULFIDES WITH CARBOXYLIC ESTERS. A CONVENIENT METHOD FOR THE PREPARATION OF THIOLESTERS
    作者:Teruaki Mukaiyama、Takeshi Takeda、Kunio Atsumi
    DOI:10.1246/cl.1974.187
    日期:1974.2.5
    In the presence of AlCl3, trimethylsilyl sulfides react with carboxylic esters to give the corresponding thiolesters in high yields.
    AlCl3 存在下,三甲基甲硅烷硫化物羧酸酯反应以高产率得到相应的硫醇酯
  • Method for producing carboxylic acid thioester
    申请人:Mitsubishi Chemical Corporation
    公开号:US10377706B2
    公开(公告)日:2019-08-13
    According to the present invention, there is provided a method for producing carboxylic acid thioester, comprising reacting a compound represented by the following formula (I), carboxylic acid and thiol in the presence of a catalyst including at least one Group 2 metal compound. The production method is a production method which is simple in reaction operation, which places a small load on the environment and the human body and which enables carboxylic acid thioester to be catalytically obtained at a high yield even at a normal temperature and a normal pressure (25° C., 1 atm). In the formula (I), R1 and R2 each independently represent a hydrocarbon group having 1 to 20 carbon atoms.
    根据本发明,提供了一种生产羧酸酯的方法,该方法包括在包括至少一种第 2 族属化合物的催化剂存在下,使下式(I)代表的化合物、羧酸醇发生反应。该生产方法反应操作简单,对环境和人体的负荷小,即使在常温常压下(25℃,1 个大气压)也能催化获得高产率的羧酸酯。在式(I)中,R1 和 R2 各自独立地代表具有 1 至 20 个碳原子的烃基。
  • Rapid and Convenient Thioester Synthesis Under Phase-Transfer Catalysis Conditions
    作者:Cristian Simion、Iwao Hashimoto、Yoshiharu Mitoma、Alina Marieta Simion、Naoyoshi Egashira
    DOI:10.1080/10426501003713072
    日期:2010.11.23
    Various thioesters were obtained through an efficient phase-transfer catalysis method, by treating several thiophenols with different acyl chlorides, in a biphasic system composed of 10% aqueous NaOH and dichloromethane in the presence of tetrabutylammonium chloride. The thiolation reaction was complete in only 5 minutes, at 0 degrees C.
  • A Convenient Method for the Preparation of Thiol Esters
    作者:Tsunco Imamoto、Masahito Kodera、Masataka Yokoyama
    DOI:10.1055/s-1982-29716
    日期:——
查看更多

同类化合物

硬脂酸对甲苯硫酯 硫基丙酸苯酯 硫代乙酸S-[4-[二(2-氯乙基)氨基]苯基]酯 硫代乙酸 S-(2-乙基苯基)酯 乙硫酸,[[(1,1-二甲基乙基)二甲基甲硅烷基]氧代]-,S-苯基酯 丙硫酸,S-(2-甲氧苯基)酯 S1,S2-二(4-氯苯基)乙烷二(硫代ate) S-苯基硫代异丁酸酯 S-苯基3-羟基硫代丁酸酯 S-苯基2-氟硫代乙酸酯 S-硫代乙酸苯酯 S-氯乙酰基-P-巯基甲苯 S-丙酰基-p-疏基甲苯 S-[4-[2-[4-(2-苯乙炔基)苯基]乙炔基]苯基]硫代乙酸酯 S-(三氟乙酰基)-4-疏基甲苯 S-(4-甲基苯基)硫代乙酸酯 S,S′-[1,4-亚苯基二(2,1-乙炔二基-4,1-亚苯基)]双(硫代乙酸酯) O-乙基S-(4-甲基苯基)单硫代草酸酯 4-溴苯基硫代乙酸酯 4-(S-乙酰基硫代)苯甲醛 4,4-二甲基-1-氧代-1-(苯基硫基)-2-戊烷基乙酸酯 3-氧代-3-(4-甲氧基苯氧基)丙酸 2-甲基苯硫酚乙酸酯 2-(氯甲酰基)-1-环戊烯-1-基硫氰酸酯 1-乙酰巯基-4-碘苯 S-(p-tolyl) cyclohexanecarbothioate 4-(2,5-Dioxo-pyrrolidin-1-yl)-thiobutyric acid S-phenyl ester S-phenyl 2-[(S)-[(2-methylpropan-2-yl)oxycarbonylamino]-phenylmethyl]-3-oxobutanethioate Tribromthioessigsaeure-phenylester Thiocrotonsaeure-S-<4-chlor>-phenylester (4S)-4-<(Z)-3-Acetoxy-2-phenylthio-2-propenoyl>-2,2-dimethyl-1,3-dioxolane (Z)-2,3,4,5,5-Pentachloro-penta-2,4-dienethioic acid S-(4-tert-butyl-phenyl) ester trans-dichlorobis(thio-L-leucine-S-phenylester-N)platinum(II) 2,3,4,5,5-Pentachlor-2,4-pentadienthiosaeure-S-(4-tolyl)ester (2Z)-2,3,4,5-tetrachloro-5-(p-tolylthio)penta-2,4-dienoyl chloride (Z)-1,3-bis(phenylthio)-5-hydroxy-2-penten-1-one (2Z,4E)-2,3,4,5-Tetrachloro-5-(4-chloro-phenylsulfanyl)-penta-2,4-dienoyl chloride S-phenyl 2-diazoethanethioate (Z)-2,3,4,5,5-Pentachloro-penta-2,4-dienethioic acid S-(4-chloro-phenyl) ester Dithiocarbonic acid S-pentachlorophenyl ester S-phenyl ester Phenyl-α-phenylacetothiol-acetat S-(2,3,4,5,6-pentachlorophenyl) (2Z)-2,3,4,5,5-pentachloropenta-2,4-dienethioate tert-butyl 2-methyl-3-oxo-3-(phenylthio)propanoate (2Z,4E)-2,3,4,5-tetrachloro-5-(phenylthio)penta-2,4-dienoyl chloride (Z)-2,3,5,5-Tetrachlor-4-phenylthio-2,4-pentadienthiosaeure-S-phenylester (Z)-2,3,4,5-Tetrachlor-5-methylthio-2,4-pentadienthiosaeure-S-pentachlorphenylester tridecanethioic acid S-phenyl ester 1,4-bis[4-(acetylsulfanyl)phenylethynyl]-2,6-di-t-butylbenzene phenyl 2,3,4,6-tetradeoxy-4-(acetylthio)-1-thio-α-D-erythro-hex-2-enopyranoside