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S-phenylisothiouronium | 36029-52-4

中文名称
——
中文别名
——
英文名称
S-phenylisothiouronium
英文别名
S-phenyl-isothiourea;S-Phenyl-isothioharnstoff;carbamimidothioic acid, phenyl ester;S-Phenyl-isothioharnstoff;S-Phenylisothioharnstoff;S-Benzyl-thioharnstoff;S-phenylisothiourea;phenyl carbamimidothioate
S-phenylisothiouronium化学式
CAS
36029-52-4
化学式
C7H8N2S
mdl
——
分子量
152.22
InChiKey
HYCHUWFLXGGFDZ-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

  • 熔点:
    206-208 °C
  • 沸点:
    264.9±23.0 °C(Predicted)
  • 密度:
    1.22±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.7
  • 重原子数:
    10
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    75.2
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    S-phenylisothiouroniumsodium ethanolate三氯氧磷 作用下, 以 乙醇 为溶剂, 生成 4-Hydrazino-2-phenylsulfanyl-pyrimidine-5-carboxylic acid ethyl ester
    参考文献:
    名称:
    Novel inhibitors of AP-1 and NF-κB mediated gene expression: structure–activity relationship studies of ethyl 4-[(3-Methyl-2,5-dioxo(3-pyrrolinyl))amino]-2-(trifluoromethyl)pyrimidine-5-carboxylate
    摘要:
    In an effort to identify novel inhibitors of AP-1 and NF-kappa B mediated transcriptional activation, several analogues of ethyl 4-[(3-methyl-2,5-dioxo(3-pyrrolinyl))amino]-2-(trifluoromethyl)pyrimidine-5-carboxylate (1) were synthesized and tested in two in vitro assays. The 2-(2'-thienyl) substituted compound (II) was identified as the most potent in this series. (C) 2000 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(00)00312-7
  • 作为产物:
    描述:
    氰胺苯硫酚乙醚 作用下, 生成 S-phenylisothiouronium
    参考文献:
    名称:
    Arndt, Justus Liebigs Annalen der Chemie, 1913, vol. 396, p. 20
    摘要:
    DOI:
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文献信息

  • 5-PROTECTED AMINOPYRIMIDINE COMPOUND, PRODUCTION METHOD THEREOF AND INTERMEDIATE THEREFOR
    申请人:TAKAHASHI Daisuke
    公开号:US20090137803A1
    公开(公告)日:2009-05-28
    The present invention provides a production method of 5-aminopyrimidine compound represented by the formula (5) by reacting a glycine compound represented by the formula (1) with t-butoxybisdimethylaminomethane, dimethylformamidedimethylacetal or dimethylformamidediethylacetal to produce a dialkylaminomethylene compound represented by the formula (2), reacting the compound of formula (2) in the presence of an acid to produce a hydroxymethylene compound represented by the formula (3), and reacting the compound of formula (3) with an amidine compound represented by the formula (4) or a salt thereof.
    本发明提供了一种生产5-氨基嘧啶化合物的方法,该化合物由式(5)表示,通过将式(1)表示的甘氨酸化合物与叔丁氧基双二甲基氨基甲烷、二甲基甲酰胺双二甲基乙酯或二甲基甲酰胺双乙基乙酯反应,以产生式(2)表示的二烷基氨甲烯化合物,然后在酸的存在下反应式(2)的化合物,以产生式(3)表示的羟甲烯化合物,最后将式(3)的化合物与式(4)表示的酰胺化合物或其盐反应。
  • PRODUCTION METHOD OF AMINOPYRIMIDINE COMPOUND
    申请人:Takahashi Daisuke
    公开号:US20090171084A1
    公开(公告)日:2009-07-02
    Aminopyrimidine compounds represented by formula (3) may be efficiently prepared by reacting an azlactone compound represented by formula (1) with an amidine compound represented by formula (2) or a salt thereof: wherein R 1 , R 2 and M are as defined in the specification.
    公式(3)所代表的氨基嘧啶化合物可以通过将公式(1)所代表的氮杂内酰亚胺化合物与公式(2)所代表的酰胺化合物或其盐反应而有效地制备:其中R1,R2和M如规范中所定义。
  • Reactions of S-acylisothioureas. II. Effects of structure and stereochemistry on the rates of hydrolysis, thiol elimination, and S to N acyl migration in acylic systems
    作者:R. F. Pratt、Thomas C. Bruice
    DOI:10.1021/ja00763a048
    日期:1972.4
  • 218. Thiadiazoles. Part VII. 5-amino-3-mercapto-1 : 2 : 4-thiadiazole derivatives
    作者:Frederick Kurzer、Sheila A. Taylor
    DOI:10.1039/jr9590001064
    日期:——
  • Radical arylation of S-allylisothiuronium chloride
    作者:L. V. Yashkina、B. V. Kopylova
    DOI:10.1007/bf00953309
    日期:1989.4
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