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(E)-7-Ethyl-2-methylundec-5-en-4-one

中文名称
——
中文别名
——
英文名称
(E)-7-Ethyl-2-methylundec-5-en-4-one
英文别名
——
(E)-7-Ethyl-2-methylundec-5-en-4-one化学式
CAS
——
化学式
C14H26O
mdl
——
分子量
210.36
InChiKey
QYAOIOBFYSRSLB-MDZDMXLPSA-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):
    5
  • 重原子数:
    15
  • 可旋转键数:
    8
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.79
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

文献信息

  • Processes for preparing beta-hydroxy-ketones and alpha,beta-unsaturated ketones
    申请人:Barnicki Donald Scott
    公开号:US20050004401A1
    公开(公告)日:2005-01-06
    Processes for producing β-hydroxy-ketones and α,β-unsaturated ketones are disclosed which comprise the crossed condensation of an aldehyde with a ketone in the presence of a hydroxide or alkoxide of alkali metal or an alkaline earth metal as catalyst. The products of the process, β-hydroxy-ketones and α,β-unsaturated ketones, are useful for the preparation of many commercially important products in the chemical process industries including solvents, drug intermediates, flavors and fragrances, other specialty chemical intermediates.
    披露了生产β-羟基酮和α,β-不饱和酮的过程,这些过程包括在碱属或碱土属的氢氧化物或醇盐的催化下,醛与酮的交叉缩合。该过程的产品,即β-羟基酮和α,β-不饱和酮,对于化学工艺工业中许多商业上重要产品的制备非常有用,包括溶剂、药物中间体、香精和香料、以及其他专用化学品中间体。
  • PROCESSES FOR PREPARING BETA-HYDROXY-KETONES AND ALPHA, BETA-UNSATURATED KETONES
    申请人:EASTMAN CHEMICAL COMPANY
    公开号:EP1638913A1
    公开(公告)日:2006-03-29
  • US6288288B1
    申请人:——
    公开号:US6288288B1
    公开(公告)日:2001-09-11
  • US6960694B2
    申请人:——
    公开号:US6960694B2
    公开(公告)日:2005-11-01
  • [EN] PROCESSES FOR PREPARING BETA-HYDROXY-KETONES AND ALPHA, BETA-UNSATURATED KETONES<br/>[FR] PROCEDES D'ELABORATION DE BETA-HYDROXY-CETONES ET DE CETONES ALPHA, BETA-INSATUREES
    申请人:EASTMAN CHEM CO
    公开号:WO2005005361A1
    公开(公告)日:2005-01-20
    Processes for producing β-hydroxy-ketones and a,β-­unsaturated ketones are disclosed which comprise the crossed condensation of an aldehyde with a ketone in the presence of a hydroxide or aikoxide of aikali metal or an aikaline earth metal as catalyst. The products of the process, β-hydroxy­ketones and a,β-unsaturated ketones, are useful for the preparation of many commercially important products in the chemical process industries including solvents, drug intermediates, flavors and fragrances, other specialty chemical intermediates.
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