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2-Cyclohexylpropan-1,1-dicarbonsaeure | 28811-74-7

中文名称
——
中文别名
——
英文名称
2-Cyclohexylpropan-1,1-dicarbonsaeure
英文别名
2-(1-Cyclohexylethyl)propanedioic acid
2-Cyclohexylpropan-1,1-dicarbonsaeure化学式
CAS
28811-74-7
化学式
C11H18O4
mdl
——
分子量
214.262
InChiKey
LVYDEOSZIIYOJO-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

计算性质

  • 辛醇/水分配系数(LogP):
    3.1
  • 重原子数:
    15
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.82
  • 拓扑面积:
    74.6
  • 氢给体数:
    2
  • 氢受体数:
    4

文献信息

  • [EN] DECARBOXYLATIVE CONJUGATE ADDITIONS AND APPLICATIONS THEREOF<br/>[FR] ADDITIONS DE CONJUGUÉS AVEC DÉCARBOXYLATION ET APPLICATIONS ASSOCIÉES
    申请人:UNIV PRINCETON
    公开号:WO2016196931A1
    公开(公告)日:2016-12-08
    Synthetic methods are described herein operable to efficiently produce a wide variety of molecular species through conjugate additions via decarboxylative mechanisms. For example, methods of functionalization of peptide residues are described, including selective functionalization of peptide C-terminal residues. In one aspect, a method of peptide functionalization comprises providing a reaction mixture including a Michael acceptor and a peptide and coupling the Michael acceptor with the peptide via a mechanism including decarboxylation of a peptide reside.
    本文描述了可操作的合成方法,能够通过脱羧机制通过共轭加成有效地产生各种分子物种。例如,描述了肽残基的官能化方法,包括对肽C-末端残基的选择性官能化。在一个方面,肽官能化方法包括提供包括迈克尔受体和肽的反应混合物,并通过包括肽残基的脱羧机制将迈克尔受体与肽偶联。
  • Decarboxylative conjugate additions and applications thereof
    申请人:The Trustees of Princeton University
    公开号:US11136349B2
    公开(公告)日:2021-10-05
    Synthetic methods are described herein operable to efficiently produce a wide variety of molecular species through conjugate additions via decarboxylative mechanisms. For example, methods of functionalization of peptide residues are described, including selective functionalization of peptide C-terminal residues. In one aspect, a method of peptide functionalization comprises providing a reaction mixture including a Michael acceptor and a peptide and coupling the Michael acceptor with the peptide via a mechanism including decarboxylation of a peptide reside.
    本文介绍的合成方法可通过脱羧机制进行共轭添加,从而有效地生产多种分子物质。例如,描述了肽残基官能化的方法,包括肽 C 端残基的选择性官能化。在一个方面,肽官能化的方法包括提供包括迈克尔受体和肽的反应混合物,并通过包括肽残基脱羧的机制将迈克尔受体与肽偶联。
  • ANTI-VIRAL COMPOUNDS
    申请人:MERRELL DOW PHARMACEUTICALS INC.
    公开号:EP0565631A1
    公开(公告)日:1993-10-20
  • DECARBOXYLATIVE CONJUGATE ADDITIONS AND APPLICATIONS THEREOF
    申请人:The Trustees of Princeton University
    公开号:US20180179248A1
    公开(公告)日:2018-06-28
    Synthetic methods are described herein operable to efficiently produce a wide variety of molecular species through conjugate additions via decarboxylative mechanisms. For example, methods of functionalization of peptide residues are described, including selective functionalization of peptide C-terminal residues. In one aspect, a method of peptide functionalization comprises providing a reaction mixture including a Michael acceptor and a peptide and coupling the Michael acceptor with the peptide via a mechanism including decarboxylation of a peptide reside.
  • US5559140A
    申请人:——
    公开号:US5559140A
    公开(公告)日:1996-09-24
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