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S-o-tolyl methanethioate | 27064-10-4

中文名称
——
中文别名
——
英文名称
S-o-tolyl methanethioate
英文别名
o-Tolylthiolformiat;S-(2-methylphenyl) methanethioate
S-o-tolyl methanethioate化学式
CAS
27064-10-4
化学式
C8H8OS
mdl
——
分子量
152.217
InChiKey
KGSBJJJGTMKGAA-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):
    2.6
  • 重原子数:
    10
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    42.4
  • 氢给体数:
    0
  • 氢受体数:
    2

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

点击查看最新优质反应信息

文献信息

  • 1,5-Di(aryl or heteroaryl)-3-halo-2(1H)-pyridones as intermediates for the preparation of AMPA receptor inhibitors
    申请人:Eisai R&D Management Co., Ltd.
    公开号:EP2177520A1
    公开(公告)日:2010-04-21
    The present invention provides compounds represented by the formula: or a salt thereof, wherein, each A1a and A3a are the same as or different from each other and each indicates an optionally substituted C6-14 aromatic hydrocarbocyclic group or 5 to 14-membered aromatic heterocyclic group; and W represents a halogen atom. The compounds are intermediates for the preparation of inhibitors of the AMPA receptor.
    本发明提供了以下式子或其盐的化合物,其中A1a和A3a分别相同或不同,每个表示一个选择性取代的C6-14芳香族烃环基或5至14元芳香族杂环基;W表示卤素原子。这些化合物是AMPA受体抑制剂的中间体。
  • Palladium-Catalyzed Thiocarbonylative Synthesis of α,β-Unsaturated Thioesters Using <i>S</i>-Aryl Thioformates as the Thioester Sources
    作者:Zekai Shen、Yong-Wang Huo、Xinxin Qi、Xiao-Feng Wu
    DOI:10.1021/acs.orglett.3c01400
    日期:2023.6.9
    A palladium-catalyzed thiocarbonylation reaction for the synthesis of α,β-unsaturated thioesters from vinyl triflates with S-aryl thioformates as the thioester sources has been developed. The reaction proceeded smoothly at low temperature, and a variety of α,β-unsaturated thioesters were produced in moderate to high yields with very good functional group tolerance. This protocol features mild reaction
    开发了一种催化的代羰基化反应,用于以甲酸 S-芳基酯为酯源,从三甲磺酸乙烯酯合成 α,β-不饱和酯。反应在低温下顺利进行,并以中等到高的产率生成了多种 α,β-不饱和酯,并且具有非常好的官能团耐受性。该方案具有温和的反应条件、良好的底物范围,并避免使用有毒的 CO 气体或有气味的醇,这使其成为通过酯转移过程合成 α、β-不饱和酯的一个有价值的补充。
  • Pd-Catalyzed Cascade Cyclization/Thiocarbonylation with Thioformates: Synthesis of Thioester-Functionalized Oxindoles
    作者:Xi-Wei Zhu、Hao Ye、Yi-Yun Pan、Yanan Wu、Xin-Xing Wu
    DOI:10.1021/acs.joc.3c02898
    日期:2024.3.1
    Pd-catalyzed thiocarbonylative cyclization of N-(o-iodoaryl)acrylamides with easily accessible thioformates has been developed. The reaction has a wide substrate scope with good yields and represents a powerful route to the synthesis of thioester-functionalized oxindoles. Both S-aryl and alkyl thioformates as the thioester sources were well tolerated. The active Pd–CO intermediate may play an important
    开发了一种 Pd 催化的 N-(邻代芳基)丙烯酰胺与容易获得的甲酸酯的代羰基环化反应。该反应具有广泛的底物范围和良好的产率,是合成酯官能化羟吲哚的有效途径。 S-芳基和甲酸烷基酯作为酯源都具有良好的耐受性。活性Pd-CO中间体可能在转化过程中发挥重要作用。
  • Palladium-Catalyzed Thiocarbonylation of Aryl Iodides with <i>S</i>-Aryl Thioformates via Thioester Transfer
    作者:Ruiting Yang、Qiumin Xie、Qian Yan、Xiuli Zhang、Bao Gao
    DOI:10.1021/acs.orglett.2c02953
    日期:2022.10.21
  • [EN] PHARMACEUTICAL COMPOSITIONS AND THEIR USES<br/>[FR] COMPOSITIONS PHARMACEUTIQUES ET UTILISATIONS ASSOCIEES
    申请人:EISAI CO LTD
    公开号:WO2003047577A2
    公开(公告)日:2003-06-12
    The present invention relates to compositions comprising 1, 2-dihydropiridin-2-one compounds and an immunoregulatory or anti-inflammatory agent. The compositions are useful for the prevention or the treatment of neurodegenerative diseases, for example demyelinating disorders.
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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