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N-cyclohexyl-2-phenylthioacetamide | 71433-02-8

中文名称
——
中文别名
——
英文名称
N-cyclohexyl-2-phenylthioacetamide
英文别名
N-Cyclohexyl-α-phenylthioacetamid;N-cyclohexyl-2-(phenylsulfanyl)acetamide;N-cyclohexyl-2-phenylsulfanylacetamide
N-cyclohexyl-2-phenylthioacetamide化学式
CAS
71433-02-8
化学式
C14H19NOS
mdl
MFCD03991357
分子量
249.377
InChiKey
IOZQXKIDAGBIQL-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:
    73-74 °C
  • 沸点:
    437.1±24.0 °C(Predicted)
  • 密度:
    1.12±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.6
  • 重原子数:
    17
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    54.4
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    N-cyclohexyl-2-phenylthioacetamide 以53%的产率得到
    参考文献:
    名称:
    HIRAI K.; IWANO Y., TETRAHEDRON LETT., 1979, NO 22, 2031-2034
    摘要:
    DOI:
  • 作为产物:
    描述:
    二乙基(苯基硫代甲基)磷酸酯环己基异氰酸酯正丁基锂 、 lithium aluminium tetrahydride 、 硫酸 作用下, 以 四氢呋喃 为溶剂, 反应 1.0h, 以79%的产率得到N-cyclohexyl-2-phenylthioacetamide
    参考文献:
    名称:
    Dephosphonylation of β-Carbonyl Phosphonates
    摘要:
    A new methodology has been developed for the P-C bond cleavage of beta-carbonyl phosphonates. The alpha,alpha-disubstituted beta-keto phosphonates and the alpha-carbamoyl phosphonates have been shown to undergo dephosphonylation by reaction of their lithium enolate with LiAlH4, followed by quenching with aqueous H2SO4, affording regioselectively alpha,alpha-disubstituted ketone and alpha-substituted and alpha,alpha-disubstituted secondary amides.
    DOI:
    10.1021/jo990221r
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文献信息

  • INHIBITORS OF 15-HYDROXYPROSTAGLANDIN DEHYDROGENASE FOR STIMULATING PIGMENTATION OF THE SKIN OR SKIN APPENDAGES
    申请人:MICHELET JEAN-FRANCOIS
    公开号:US20110014250A1
    公开(公告)日:2011-01-20
    Inhibitors of 15-hydroxyprostaglandin dehydrogenase (15-PGDH), for example tetrazole, styrylpyrazole, phenylfuran, phenylthiophene, phenylpyrrazole, pyrazolecarboxamide, 2-thioacetamide and azo compounds, are useful for promoting or stimulating pigmentation of the skin and/or skin appendages and/or for preventing and/or for limiting depigmentation and/or whitening of the skin and/or skin appendages, notably for preventing and/or limiting canities.
    15-羟基前列腺素脱氢酶(15-PGDH)的抑制剂,例如四唑、苯乙烯吡唑、苯并呋喃、苯并硫吩、苯并吡唑、吡唑羧酰胺、2-硫代乙酰胺和偶氮化合物,可用于促进或刺激皮肤和/或皮肤附属物的色素沉着,或预防和/或限制皮肤和/或皮肤附属物的脱色和/或变白,特别是预防和/或限制白发。
  • Utilisation d'un inhibiteur de 15-hydroxy prostaglandine déshydrogénase pour favoriser la pigmentation de la peau ou des phanères
    申请人:L'Oréal
    公开号:EP1594438B1
    公开(公告)日:2013-07-17
  • US7705041B2
    申请人:——
    公开号:US7705041B2
    公开(公告)日:2010-04-27
  • US8735445B2
    申请人:——
    公开号:US8735445B2
    公开(公告)日:2014-05-27
  • Dephosphonylation of β-Carbonyl Phosphonates
    作者:Shi Yong Lee、Chi-Wan Lee、Dong Young Oh
    DOI:10.1021/jo990221r
    日期:1999.9.1
    A new methodology has been developed for the P-C bond cleavage of beta-carbonyl phosphonates. The alpha,alpha-disubstituted beta-keto phosphonates and the alpha-carbamoyl phosphonates have been shown to undergo dephosphonylation by reaction of their lithium enolate with LiAlH4, followed by quenching with aqueous H2SO4, affording regioselectively alpha,alpha-disubstituted ketone and alpha-substituted and alpha,alpha-disubstituted secondary amides.
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