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1-(2,5-Dichlorothiophen-3-yl)-2-phenylsulfanylethanone | 1152657-02-7

中文名称
——
中文别名
——
英文名称
1-(2,5-Dichlorothiophen-3-yl)-2-phenylsulfanylethanone
英文别名
——
1-(2,5-Dichlorothiophen-3-yl)-2-phenylsulfanylethanone化学式
CAS
1152657-02-7
化学式
C12H8Cl2OS2
mdl
MFCD12740730
分子量
303.233
InChiKey
CVKGABNRRBAJNZ-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:
    406.0±45.0 °C(predicted)
  • 密度:
    1.46±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.4
  • 重原子数:
    17
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.083
  • 拓扑面积:
    70.6
  • 氢给体数:
    0
  • 氢受体数:
    3

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

反应信息

  • 作为反应物:
    描述:
    1-(2,5-Dichlorothiophen-3-yl)-2-phenylsulfanylethanone盐酸羟胺 作用下, 生成 N-[1-(2,5-dichlorothiophen-3-yl)-2-phenylsulfanylethylidene]hydroxylamine
    参考文献:
    名称:
    Ago-allosteric modulators of human glucagon-like peptide 2 receptor
    摘要:
    Glucagon-like peptide 2 (GLP-2) is an intestinotropic peptide that binds to GLP-2 receptor (GLP-2R), a class-B G protein-coupled receptor (GPCR). Few synthetic agonists have been reported so far for class-B GPCRs. Here, we report the first scaffold compounds of ago-allosteric modulators for human GLP-2R, derived from methyl 2-{[(2Z)-2-(2,5-dichlorothiophen-3-yl)-2-(hydroxyimino) ethyl] sulfanyl}benzoate (compound 1). (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2012.08.026
  • 作为产物:
    描述:
    苯酚 在 sodium hydride 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 生成 1-(2,5-Dichlorothiophen-3-yl)-2-phenylsulfanylethanone
    参考文献:
    名称:
    Ago-allosteric modulators of human glucagon-like peptide 2 receptor
    摘要:
    Glucagon-like peptide 2 (GLP-2) is an intestinotropic peptide that binds to GLP-2 receptor (GLP-2R), a class-B G protein-coupled receptor (GPCR). Few synthetic agonists have been reported so far for class-B GPCRs. Here, we report the first scaffold compounds of ago-allosteric modulators for human GLP-2R, derived from methyl 2-{[(2Z)-2-(2,5-dichlorothiophen-3-yl)-2-(hydroxyimino) ethyl] sulfanyl}benzoate (compound 1). (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2012.08.026
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文献信息

  • Ago-allosteric modulators of human glucagon-like peptide 2 receptor
    作者:Kazuto Yamazaki、Hiroki Terauchi、Daisuke Iida、Hironori Fukumoto、Shuichi Suzuki、Takaki Kagaya、Mika Aoki、Koichiro Koyama、Takashi Seiki、Kazuma Takase、Misako Watanabe、Tohru Arai、Kappei Tsukahara、Junichi Nagakawa
    DOI:10.1016/j.bmcl.2012.08.026
    日期:2012.10
    Glucagon-like peptide 2 (GLP-2) is an intestinotropic peptide that binds to GLP-2 receptor (GLP-2R), a class-B G protein-coupled receptor (GPCR). Few synthetic agonists have been reported so far for class-B GPCRs. Here, we report the first scaffold compounds of ago-allosteric modulators for human GLP-2R, derived from methyl 2-[(2Z)-2-(2,5-dichlorothiophen-3-yl)-2-(hydroxyimino) ethyl] sulfanyl}benzoate (compound 1). (C) 2012 Elsevier Ltd. All rights reserved.
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