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S-(4-chlorophenyl) 2-methylpropanethioate | 56421-91-1

中文名称
——
中文别名
——
英文名称
S-(4-chlorophenyl) 2-methylpropanethioate
英文别名
S-4-chlorophenyl 2-methylpropanethioate;thioisobutyric acid S-(4-chloro-phenyl ester);Thioisobuttersaeure-S-(4-chlor-phenylester);p-Chlorphenylisothiobutyrat
S-(4-chlorophenyl) 2-methylpropanethioate化学式
CAS
56421-91-1
化学式
C10H11ClOS
mdl
——
分子量
214.716
InChiKey
WZWRUNILMCILDX-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:
    147-148 °C(Press: 13 Torr)
  • 密度:
    1.1676 g/cm3

计算性质

  • 辛醇/水分配系数(LogP):
    3.61
  • 重原子数:
    13.0
  • 可旋转键数:
    2.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    17.07
  • 氢给体数:
    0.0
  • 氢受体数:
    2.0

反应信息

  • 作为产物:
    描述:
    cis-N.N-Dimethyl-N-<(1.1-dimethyl-2-(p-chlorphenyl)-thio)-cyclopropyl>-amin 在 氧气 、 rose bengal 作用下, 以 甲醇 为溶剂, 生成 S-(4-chlorophenyl) 2-methylpropanethioate
    参考文献:
    名称:
    Cleavage of a cyclopropane ring by singlet oxygen
    摘要:
    DOI:
    10.1021/jo00909a014
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文献信息

  • Manganese(<scp>iii</scp>)-promoted thiocarbonylation of alkylborates with disulfides: synthesis of aliphatic thioesters
    作者:Bo Chen、Xiao-Feng Wu
    DOI:10.1039/d1ob01960k
    日期:——
    A Mn(III)-promoted thiocarbonylation procedure toward the synthesis of thioesters has been developed. By employing easily available disulfides and potassium alkyltrifluoroborates as the starting materials, and cheap and non-toxic Mn(OAc)3·2H2O as the promotor, a broad range of thioesters were synthesized in good to excellent yields via radical intermediates.
    已开发出一种用于合成硫酯的 Mn( III ) 促进的硫代羰基化过程。以易得的二硫化物和烷基三氟硼酸钾为起始原料,以廉价且无毒的Mn(OAc) 3 ·2H 2 O为促进剂,通过自由基中间体以良好至优异的产率合成了多种硫酯。
  • A New and Efficient Esterification Reaction via Mixed Anhydrides by the Promotion of a Catalytic Amount of Lewis Acid
    作者:Mitsutomo Miyashita、Isamu Shiina、So Miyoshi、Teruaki Mukaiyama
    DOI:10.1246/bcsj.66.1516
    日期:1993.5
    In the presence of a catalytic amount of Lewis acid, various carboxylic esters or S-phenyl carbothioates are prepared in excellent yields by the respective reactions of equimolar amounts of silyl carboxylates and alkyl silyl ethers or phenyl silyl sulfides with 4-trifluoromethylbenzoic anhydride.
    在催化量的路易斯酸存在下,通过等摩尔量的甲硅烷基羧酸酯和烷基甲硅烷基醚或苯基甲硅烷基硫化物与4-三氟甲基苯甲酸酐的相应反应,以极好的收率制备各种羧酸酯或S-苯基硫代碳酸酯。
  • A New and Efficient Method for the Preparation of<i>S</i>-Phenyl Carbothioates via Mixed Anhydrides Using Active Titanium(IV) Salts
    作者:Teruaki Mukaiyama、Mitsutomo Miyashita、Isamu Shiina
    DOI:10.1246/cl.1992.1747
    日期:1992.9
    In the presence of a catalytic amount of titanium(IV) salt, various S-phenyl carbothioates are prepared in excellent yields by the reaction of nearly equimolar amounts of silyl derivatives of carboxylic acids and benzenethiols with p-trifluoromethylbenzoic anhydride.
    在催化量的钛 (IV) 盐的存在下,通过几乎等摩尔量的羧酸和苯硫醇的甲硅烷基衍生物与对三氟甲基苯甲酸酐反应,可以以极好的收率制备各种 S-苯基硫代碳酸酯。
  • Some New Thiol Esters. Preparation of Dithiolfumarates
    作者:Gene Sumrell、Morris Zief、Earl J. Huber、George E. Ham、Charles H. Schramm
    DOI:10.1021/ja01525a052
    日期:1959.8
  • ALIEV I. A.; SULTANOV YU. M., ELMI EHSEHRLEHR. AZEHRB. UNIV. KIMJA ELMLEHRI CEP., NAUCH. TR. AZERB. YH-+
    作者:ALIEV I. A.、 SULTANOV YU. M.
    DOI:——
    日期:——
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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