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3-hydroxy-2-methylheptanoic acid | 80458-09-9

中文名称
——
中文别名
——
英文名称
3-hydroxy-2-methylheptanoic acid
英文别名
——
3-hydroxy-2-methylheptanoic acid化学式
CAS
80458-09-9
化学式
C8H16O3
mdl
——
分子量
160.213
InChiKey
VBFGDSCDTYAEBA-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):
    1.5
  • 重原子数:
    11
  • 可旋转键数:
    5
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.88
  • 拓扑面积:
    57.5
  • 氢给体数:
    2
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    ethyl 3-hydroxy-2-methylheptanoate 在 甲醇 、 sodium hydroxide 作用下, 以 四氢呋喃 为溶剂, 反应 5.0h, 以28%的产率得到3-hydroxy-2-methylheptanoic acid
    参考文献:
    名称:
    Linfuranones B and C, Furanone-Containing Polyketides from a Plant-Associated Sphaerimonospora mesophila
    摘要:
    Two new furanone-containing polyketides, linfuranones B and C, were isolated from a plant-associated actinomycete of the genus Sphaerimonospora. Their structures were determined by NMR and MS spectroscopic analyses, and the absolute configurations were established by anisotropic methods and chemical degradation approaches. In silico analysis of biosynthetic genes suggested that linfuranone B is generated from linfuranone C by oxidative cleavage of the polyketide chain. Linfuranones B and C induced preadipocyte differentiation into matured adipocytes at 20-40 mu M without showing cytotoxicity.
    DOI:
    10.1021/acs.jnatprod.8b00071
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文献信息

  • SYNTHESIS OF OLIGOKETIDES
    申请人:Kosan Biosciences
    公开号:EP1144375A2
    公开(公告)日:2001-10-17
  • JPH0339094A
    申请人:——
    公开号:JPH0339094A
    公开(公告)日:1991-02-20
  • US6225438B1
    申请人:——
    公开号:US6225438B1
    公开(公告)日:2001-05-01
  • [EN] SYNTHESIS OF OLIGOKETIDES<br/>[FR] SYNTHESE DE POLYCETIDES
    申请人:KOSAN BIOSCIENCES INC
    公开号:WO2000044717A2
    公开(公告)日:2000-08-03
    Facile methods for preparing diketide and triketide thioesters are disclosed. The resulting thioesters may be used as intermediates in the synthesis of desired polyketides, and may contain functional groups which ultimately reside in side chains on the resulting polyketide and thus can be used further to manipulate the polyketide so as to form derivatives. The polyketides produced may also be tailored by glycosylation, hydroxylation and the like. New polyketides and their derivatives and tailored forms are thereby produced.
  • [EN] MEDIUM CHAIN LENGTH PHA COPOLYMER AND PROCESS FOR PRODUCING SAME<br/>[FR] COPOLYMERE PHA A LONGUEUR DE CHAINE MOYENNE ET PROCEDE DE PRODUCTION DE CELUI-CI
    申请人:PROCTER & GAMBLE
    公开号:WO2001055436A1
    公开(公告)日:2001-08-02
    Poly-3-hydroxyalkanoates (PHAs) that includes medium length 3-hydroxyacyl monomers and a process for producing the same comprising culturing a microorganism with a medium chain fatty carbon source and a fatty acid oxidation inhibitor. Using the process of this invention, microorganisms which normally incorporate only short chain fatty acids, produce PHAs containing short and medium chain 3-hydroxyacyl monomers.
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