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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

  • 作为反应物:
    描述:
    S-o-tolyl methanethioate五氯化磷 作用下, 生成 o-Tolyldichlormethylsulfid
    参考文献:
    名称:
    Holsboer,D.H.; van der Veek,A.P.M., Recueil des Travaux Chimiques des Pays-Bas, 1972, vol. 91, p. 349 - 356
    摘要:
    DOI:
  • 作为产物:
    描述:
    参考文献:
    名称:
    Bax,P.C.; Stevens,W., Recueil des Travaux Chimiques des Pays-Bas, 1970, vol. 89, p. 265 - 269
    摘要:
    DOI:
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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
    开发了一种钯催化的硫代羰基化反应,用于以硫代甲酸 S-芳基酯为硫酯源,从三氟甲磺酸乙烯酯合成 α,β-不饱和硫酯。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-不饱和硫酯,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 气体或有气味的硫醇,这使其成为通过硫酯转移过程合成 α、β-不饱和硫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-(邻碘代芳基)丙烯酰胺与容易获得的硫代甲酸酯的硫代羰基环化反应。该反应具有广泛的底物范围和良好的产率,是合成硫酯官能化羟吲哚的有效途径。 S-芳基和硫代甲酸烷基酯作为硫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

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 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 1-乙酰巯基-4-碘苯 S-(2-methoxyphenyl) 4-cyclopropylidenebutanethioate phenyl 3-methyl-2-cyclohexene-1-carbothioate S-(2-fluorophenyl) 2-methylpropanethioate 2-isopropylidenedithiosuccinic acid di-S-(4-fluorophenyl) ester thioacetic acid S-(4-ethyl-phenyl ester) S-phenyl 2,3-dimethyl-2-butenethioate 3-phenylsulfanylcarbonyl-propionic acid ethyl ester S-phenyl (3r,5r,7r)-adamantane-1-carbothioate (E)-S-Phenyl 4,4-dimethylpent-2-enethioate S-phenyl 2-(2-methoxyphenyl)ethanethioate S-phenyl (2R,3R)-3-(tert-butyldimethylsiloxy)-2-methyl-3-phenylpropanethioate S-(4-fluorophenyl) thiopivalate S-phenyl 2-methylbutanethioate S-phenyl 3-(phenyl((trimethylsilyl)oxy)amino)-3-(thiophen-2-yl)propanethioate S-phenyl 3-(4-bromophenyl)-3-(phenyl((trimethylsilyl)oxy)amino)propanethioate S-phenyl 3-phenyl-3-(phenyl((triethylsilyl)oxy)amino)propanethioate S-phenyl 3-cyclohexyl-3-(phenyl((trimethylsilyl)oxy)amino)propanethioate S-phenyl 3-(((tert-butyldimethylsilyl)oxy)(phenyl)amino)-3-phenylpropanethioate S-phenyl 3-(4-methoxyphenyl)-3-(phenyl((trimethylsilyl)oxy)amino)propanethioate S-phenyl 3-(phenyl((trimethylsilyl)oxy)amino)-3-(p-tolyl)propanethioate S-phenyl 3-(4-fluorophenyl)-3-(phenyl((trimethylsilyl)oxy)amino)propanethioate S-phenyl 3-phenyl-3-(phenyl((trimethylsilyl)oxy)amino)propanethioate (E)-S-phenyl 5-phenyl-3-(phenyl((trimethylsilyl)oxy)amino)pent-4-enethioate S-phenyl 3-hydroxy-3-(4-methoxyphenyl)propanethioate S-phenyl 2-methyl-3-oxobutanethioate S-phenyl O-acetyl(thioglycolate) 6-Nitro-9-oxodecansaeure-phenylthioester 2-isopropylidenedithiosuccinic acid di-S-p-tolyl ester