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6-(2-phenylethyl)-pyrimidin-4-ol | 1258306-09-0

中文名称
——
中文别名
——
英文名称
6-(2-phenylethyl)-pyrimidin-4-ol
英文别名
6-(2-Phenylethyl)-pyrimidin-4-ol;4-(2-phenylethyl)-1H-pyrimidin-6-one
6-(2-phenylethyl)-pyrimidin-4-ol化学式
CAS
1258306-09-0
化学式
C12H12N2O
mdl
——
分子量
200.24
InChiKey
UJYSNKMPVRIVPH-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:
    217-219 °C (decomp)
  • 沸点:
    350.3±35.0 °C(Predicted)
  • 密度:
    1.14±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.5
  • 重原子数:
    15
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    41.5
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    参考文献:
    名称:
    Synthesis of β-Keto Esters In-Flow and Rapid Access to Substituted Pyrimidines
    摘要:
    We have developed an in-flow process for the synthesis of beta-keto esters via the BF3 center dot OEt2-catalyzed formal C-H insertion of ethyl diazoacetate into aldehydes. The beta-keto esters were then condensed with a range of amidines to give a variety of 2,6-substituted pyrimidin-4-ols.
    DOI:
    10.1021/jo101783m
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文献信息

  • AZA PYRIDONE ANALOGS USEFUL AS MELANIN CONCENTRATING HORMONE RECEPTOR-1 ANTAGONISTS
    申请人:Ahmad Saleem
    公开号:US20110319439A1
    公开(公告)日:2011-12-29
    MCHR1 antagonists are provided having the following Formula I: wherein all of the variables are defined herein. Such compounds are useful for the treatment of MCHR1 mediated diseases, such as obesity, diabetes, IBD, depression, and anxiety.
    提供以下式子I的MCHR1拮抗剂:其中所有变量在此定义。这些化合物对于治疗MCHR1介导的疾病如肥胖症,糖尿病,炎症性肠病,抑郁症和焦虑症非常有用。
  • US8278316B2
    申请人:——
    公开号:US8278316B2
    公开(公告)日:2012-10-02
  • Synthesis of β-Keto Esters In-Flow and Rapid Access to Substituted Pyrimidines
    作者:Hannah E. Bartrum、David C. Blakemore、Christopher J. Moody、Christopher J. Hayes
    DOI:10.1021/jo101783m
    日期:2010.12.17
    We have developed an in-flow process for the synthesis of beta-keto esters via the BF3 center dot OEt2-catalyzed formal C-H insertion of ethyl diazoacetate into aldehydes. The beta-keto esters were then condensed with a range of amidines to give a variety of 2,6-substituted pyrimidin-4-ols.
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