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1-cyclohexyl-hexan-1-ol | 53398-70-2

中文名称
——
中文别名
——
英文名称
1-cyclohexyl-hexan-1-ol
英文别名
Cyclohexyl hexanol;1-cyclohexylhexan-1-ol
1-cyclohexyl-hexan-1-ol化学式
CAS
53398-70-2
化学式
C12H24O
mdl
——
分子量
184.322
InChiKey
YOGRLTXNCLHZFR-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):
    4.3
  • 重原子数:
    13
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    1-cyclohexyl-hexan-1-ol戴斯-马丁氧化剂 作用下, 以 二氯甲烷 为溶剂, 反应 0.5h, 以87%的产率得到1-环己基己烷-1-酮
    参考文献:
    名称:
    Comparative inhibition of tetrameric carbonyl reductase activity in pig heart cytosol by alkyl 4-pyridyl ketones
    摘要:
    Context and objective: The present study is to elucidate the comparative inhibition of tetrameric carbonyl reductase (TCBR) activity by alkyl 4-pyridyl ketones, and to characterize its substrate-binding domain.Materials and methods: The inhibitory effects of alkyl 4-pyridyl ketones on the stereoselective reduction of 4-benzoylpyridine (4-BP) catalyzed by TCBR were examined in the cytosolic fraction of pig heart.Results: Of alkyl 4-pyridyl ketones, 4-hexanoylpyridine, which has a straight-chain alkyl group of five carbon atoms, inhibited most potently TCBR activity and was a competitive inhibitor. Furthermore, cyclohexyl pentyl ketone, which is substituted by cyclohexyl group instead of phenyl group of hexanophenone, had much lower ability to be reduced than hexanophenone.Discussion and conclusion: These results suggest that in addition to a hydrophobic cleft corresponding to a straight-chain alkyl group of five carbon atoms, a hydrophobic pocket with affinity for an aromatic group is located in the substrate-binding domain of TCBR.
    DOI:
    10.3109/14756366.2013.790021
  • 作为产物:
    描述:
    alkaline earth salt of/the/ methylsulfuric acid 在 甲醇 作用下, 生成 1-cyclohexyl-hexan-1-ol
    参考文献:
    名称:
    Braude et al., Journal of the Chemical Society, 1952, p. 1419,1424
    摘要:
    DOI:
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文献信息

  • Novel Syntheses of Secondary and Tertiary Alcohols from Alkynes via the Hydroboration Reaction
    作者:George ZWEIFEL、Richard P. FISHER
    DOI:10.1055/s-1974-23307
    日期:——
  • PARTICLES HAVING HYDROPHOBIC MATERIAL THEREIN
    申请人:AUSTRALIAN NUCLEAR SCIENCE AND TECHNOLOGY ORGANISATION
    公开号:EP1906915A1
    公开(公告)日:2008-04-09
  • Solution for immersion exposure and immersion exposure method
    申请人:Kagayama Akifumi
    公开号:US20090130604A1
    公开(公告)日:2009-05-21
    The object is to resolve a finer pattern with a narrower line/space width by immersion lithography technology in the manufacture of a semiconductor or the like. A liquid for use in immersion exposure includes a saturated hydrocarbon compound as a main component, wherein the content of an impurity or impurities having an unsaturated bond or a heteroatom in its structure is respectively as follows: (i) 2 μg/mL or less in total for a compound having a conjugated unsaturated bond; (ii) 30 μg/mL or less in total for a compound having no conjugated unsaturated bond but having a non-conjugated unsaturated bond; (iii) 15 μg/mL or less in total for amines having no unsaturated bond; and (iv) 100 μg/mL or less in total for a heterocyclic compound, alcohols, ethers and a halogen-containing compound, other than above compounds (i) to (iii).
  • US4767883A
    申请人:——
    公开号:US4767883A
    公开(公告)日:1988-08-30
  • US5674987A
    申请人:——
    公开号:US5674987A
    公开(公告)日:1997-10-07
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