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(4-chloro-phenyl)-thioacetic acid S-phenyl ester | 100623-07-2

中文名称
——
中文别名
——
英文名称
(4-chloro-phenyl)-thioacetic acid S-phenyl ester
英文别名
(4-chloro-phenyl)-thioacetic acid S-phenyl ester;(4-Chlor-phenyl)-thioessigsaeure-S-phenylester
(4-chloro-phenyl)-thioacetic acid S-phenyl ester化学式
CAS
100623-07-2
化学式
C14H11ClOS
mdl
——
分子量
262.76
InChiKey
CFQYZPPAFRNLJQ-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:
    17.0
  • 可旋转键数:
    3.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    17.07
  • 氢给体数:
    0.0
  • 氢受体数:
    2.0

反应信息

  • 作为反应物:
    描述:
    N-亚苄基-4-甲基苯磺酰胺(4-chloro-phenyl)-thioacetic acid S-phenyl ester 在 1-[3,5-bis(trifluoromethyl)phenyl]-3-[4-[(S)-[(2R,4S,5R)-5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl]-(naphthalen-1-ylmethoxy)methyl]quinolin-6-yl]urea 作用下, 以 乙醚 为溶剂, 反应 48.08h, 以90%的产率得到S-phenyl (2S,3S)-2-(4-chlorophenyl)-3-[(4-methylphenyl)sulfonamido]-3-phenylpropanethioate
    参考文献:
    名称:
    双功能有机催化剂催化S-苯基硫代酸酯的立体选择性曼尼希反应
    摘要:
    AbstractA highly stereoselective Mannich reaction of S‐phenyl thioesters was achieved by using bifunctional thiourea catalysts. Using a quinine‐derived C6′‐urea catalyst, the direct Mannich products of N‐tosyl imines and S‐phenyl thioesters were obtained in high yields and excellent diastereo‐ and enantioselectivities.magnified image
    DOI:
    10.1002/adsc.201400735
  • 作为产物:
    参考文献:
    名称:
    有机硫化物对温室红蜘蛛螨卵和幼虫的毒性。II.- 其他硫化物
    摘要:
    列出并讨论了许多化合物对温室红蜘蛛 (Tetranychus telarius L.) 的卵和幼螨的活性,这些化合物均包含通过各种含硫桥连接的两个苯核。
    DOI:
    10.1002/jsfa.2740081003
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文献信息

  • An Efficient Synthesis of Thioesters Via TFA-Catalyzed Reaction of Carboxylic Acid and Thiols: Remarkably Facile C–S Bond Formation
    作者:Adel S. El-Azab、Alaa A.-M. Abdel-Aziz
    DOI:10.1080/10426507.2012.664220
    日期:2012.9.1
    Abstract A general, facile, and efficient new synthetic path to thioesters was established by employing defined TFA-catalyzed reaction of carboxylic acid and thiol under mild conditions. The structure of the newly synthesized compounds was determined by infrared spectroscopy, nuclear magnetic resonance, and a single crystal X-ray crystallographic analysis. Supplemental materials are available for this
    摘要 通过在温和条件下采用特定的三氟乙酸催化羧酸醇的反应,建立了一种通用、简便、高效的酯合成新途径。新合成化合物的结构通过红外光谱、核磁共振和单晶 X 射线晶体学分析确定。补充材料可用于本文。转至出版商在线版的及相关元素,查看免费的补充文件。图形概要
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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