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5-羟基庚烷-2-酮 | 37902-41-3

中文名称
5-羟基庚烷-2-酮
中文别名
——
英文名称
5-hydroxyheptan-2-one
英文别名
——
5-羟基庚烷-2-酮化学式
CAS
37902-41-3
化学式
C7H14O2
mdl
——
分子量
130.187
InChiKey
MQRALIJAASQPNT-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:
    219.5±23.0 °C(Predicted)
  • 密度:
    0.935±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.5
  • 重原子数:
    9
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.86
  • 拓扑面积:
    37.3
  • 氢给体数:
    1
  • 氢受体数:
    2

SDS

SDS:d4dd8de9c64e0580215d0b09504228c9
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反应信息

  • 作为反应物:
    描述:
    5-羟基庚烷-2-酮 在 lithium aluminium tetrahydride 作用下, 以 四氢呋喃 为溶剂, 生成 2,5-庚二醇
    参考文献:
    名称:
    Intramolecular H-transfer reactions during the Decomposition of Alkylhydroperoxides in hydrocarbons as the solvents
    摘要:
    DOI:
    10.1002/prac.19943360109
  • 作为产物:
    参考文献:
    名称:
    Intramolecular H-transfer reactions during the Decomposition of Alkylhydroperoxides in hydrocarbons as the solvents
    摘要:
    DOI:
    10.1002/prac.19943360109
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文献信息

  • Fluorination or hydroxylation of non activated CH bonds in amides and ketones using CCl4 or NBS in superacids
    作者:Agnès Martin、Marie-Paule Jouannetaud、Jean-Claude Jacquesy
    DOI:10.1016/0040-4039(96)00475-3
    日期:1996.4
    Amides and ketones are fluorinated or hydroxylated in HF-SbF5 in the presence of CCl4 or NBS, reaction occurring at a carbon far located from the functional group.
    在CCl 4或NBS的存在下,酰胺和酮在HF-SbF 5中被化或羟基化,反应发生在远离官能团的碳上。
  • Functionalization of non-activated C–H bonds in ketones and imines with HF/SbF5/CCl4
    作者:Sébastien Thibaudeau、Agnès Martin-Mingot、Marie-Paule Jouannetaud、J.C Jacquesy
    DOI:10.1016/s0040-4020(02)00692-0
    日期:2002.8
    Reaction of cyclic ketones 2–6 and imines 15–17 in HF/SbF5 in presence of CCl4 yield hydroxy or fluoroderivatives, hydride abstraction occurring at a site located far from the functional group. Whereas ketones 2–5 yield only hydroxy derivatives, through cyclic carboxonium ion, imines 15, 16 N-protonated in the media conditions give only fluoroderivatives 18, 19, respectively, after quenching with HF–pyridine
    环酮的反应2 - 6和亚胺15 - 17中HF /的SbF 5在四氯化碳的存在4产率羟基或fluoroderivatives,氢化物提取在位于远离官能团的位点发生。而酮2 - 5产率只有羟基衍生物,通过环状carboxonium离子,亚胺15,16的N-质子化的培养基条件只给出fluoroderivatives 18,19分别与HF-吡啶淬火后。当从大分子环酮24和24开始时,环收缩是有效的。25和亚胺26生成羟基或环己酮和/或环庚酮的混合物。
  • TWO-CYCLE LUBRICANTS AND METHODS OF USING THE SAME
    申请人:THE LUBRIZOL CORPORATION
    公开号:EP0552334A1
    公开(公告)日:1993-07-28
  • Use of a TRPM5 Inhibitor to Regulate Insulin and GLP-1 Release
    申请人:Lee S. Paul
    公开号:US20080306030A1
    公开(公告)日:2008-12-11
    The present invention is directed to methods of enhancing insulin release, GLP-1 release, and insulin sensitivity, methods of increasing insulin gene expression, methods of decreasing gastric secretion and emptying and glucagons secretion, and methods of inhibiting food intake, and methods of treating diabetes mellitus, insulin resistance syndrome, hyperglycemia, and obesity comprising administering to a subject an effective amount of a TRPM5 inhibitor.
  • US8193168B2
    申请人:——
    公开号:US8193168B2
    公开(公告)日:2012-06-05
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