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Methyl hexadecanoate; methyl octadecanoate

中文名称
——
中文别名
——
英文名称
Methyl hexadecanoate; methyl octadecanoate
英文别名
methyl hexadecanoate;methyl octadecanoate
Methyl hexadecanoate; methyl octadecanoate化学式
CAS
——
化学式
C36H72O4
mdl
——
分子量
569.0
InChiKey
XICSTKPMYLWLBF-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):
    12.06
  • 重原子数:
    40
  • 可旋转键数:
    32
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.94
  • 拓扑面积:
    52.6
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

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文献信息

  • Fractionation of alkyl carboxylate mixtures
    申请人:THE PROCTER & GAMBLE COMPANY
    公开号:EP0062113B1
    公开(公告)日:1985-09-25
  • REACTIONS IN THE PRESENCE OF RUTHENIUM COMPLEXES
    申请人:California Institute of Technology
    公开号:EP3129347A1
    公开(公告)日:2017-02-15
  • METHOD FOR PRODUCING SOPHOROSE LIPID
    申请人:Yanagisawa Satohiro
    公开号:US20110237531A1
    公开(公告)日:2011-09-29
    The present invention provides a low-cost, efficient method for producing a glycolipid biosurfactant, in particular, lactonic sophorose lipids. This method is characterized by culturing a microorganism capable of producing the biosurfactant under limited oxygen supply. The present invention enables preferential production of lactonic sophorose lipids and facilitates recovery of the lactonic sophorose lipids in a solid form. Further, the present invention enables production of high purity acidic sophorose lipids by hydrolyzing high purity lactonic sophorose lipids produced by the above method. The present invention also provides lactonic sophorose lipids that possess strong antibacterial and antifungal activities, and an antibacterial and/or antifungal agent containing the sophorose lipids.
  • US8664373B2
    申请人:——
    公开号:US8664373B2
    公开(公告)日:2014-03-04
  • [EN] REACTIONS IN THE PRESENCE OF RUTHENIUM COMPLEXES<br/>[FR] RÉACTIONS EN PRÉSENCE DE COMPLEXES DE RUTHÉNIUM
    申请人:CALIFORNIA INST OF TECHN
    公开号:WO2015157736A1
    公开(公告)日:2015-10-15
    Described herein are compounds and methods for catalyzing metathesis reactions. The compounds described herein are ruthenium complexes bearing cyclic alkyl amino carbene (CAAC) ligands. The ruthenium complexes bearing cyclic alkyl amino carbene ligands may be used for catalyzing metathesis reactions, such as ethenolysis and alkenolysis reactions.
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