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N-Methyl-N-butyryl-aminoacetonitril | 36801-51-1

中文名称
——
中文别名
——
英文名称
N-Methyl-N-butyryl-aminoacetonitril
英文别名
N-(cyanomethyl)-N-methylbutanamide
N-Methyl-N-butyryl-aminoacetonitril化学式
CAS
36801-51-1
化学式
C7H12N2O
mdl
——
分子量
140.185
InChiKey
CPWKVGXAMUOBKH-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:
    257.3±23.0 °C(Predicted)
  • 密度:
    0.988±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.3
  • 重原子数:
    10
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.71
  • 拓扑面积:
    44.1
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • IMIDAZO[1,2-A]PYRIDINE DERIVATIVES: PREPARATION AND PHARMACEUTICAL APPLICATIONS
    申请人:MEI Pharma, Inc.
    公开号:EP1863811B1
    公开(公告)日:2014-03-12
  • IMIDAZO[1,2-a]PYRIDINE DERIVATIVES: PREPARATION AND PHARMACEUTICAL APPLICATIONS
    申请人:MEI Pharma, Inc.
    公开号:US20150038703A1
    公开(公告)日:2015-02-05
    The present invention relates to hydroxamate compounds which are inhibitors of histone deacetylase. More particularly, the present invention relates to imidazo[1,2-a]pyridine containing compounds and methods for their preparation. These compounds may be useful as medicaments for the treatment of proliferative disorders as well as other diseases involving, relating to or associated with enzymes having histone deacetylase activities (HDAC).
  • SUBSTITUTED PYRAZOLO-PYRIDINE AMIDES AND THEIR USE AS GLUN2B RECEPTOR MODULATORS
    申请人:JANSSEN PHARMACEUTICA NV
    公开号:US20210017168A1
    公开(公告)日:2021-01-21
    Substituted Pyrazolo-pyridines as GluN2B receptor ligands. Such compounds may be used in GluN2B receptor modulation and in pharmaceutical compositions and methods for the treatment of disease states, disorders, and conditions mediated by GluN2B receptor activity.
  • US8648092B2
    申请人:——
    公开号:US8648092B2
    公开(公告)日:2014-02-11
  • US9266882B2
    申请人:——
    公开号:US9266882B2
    公开(公告)日:2016-02-23
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