摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

1-(1-环戊烯基)-3-丙烯-1-醇 | 69042-24-6

中文名称
1-(1-环戊烯基)-3-丙烯-1-醇
中文别名
——
英文名称
1-(1-cyclopentenyl)-3-propen-1-ol
英文别名
1-cyclopent-1-enyl-allyl alcohol;1-Cyclopent-1-enyl-allylalkohol;1--propen-(2)-ol-(1);1-(1-Cyclopentenyl)-2-propen-1-ol;1-(Cyclopenten-1-yl)prop-2-en-1-ol
1-(1-环戊烯基)-3-丙烯-1-醇化学式
CAS
69042-24-6
化学式
C8H12O
mdl
——
分子量
124.183
InChiKey
NYGRFASZFWUCAJ-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):
    1.4
  • 重原子数:
    9
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

点击查看最新优质反应信息

文献信息

  • [EN] A PROCESS FOR THE PREPARATION OF ALKYLIDENECYCLOPENTANONE DERIVATIVES<br/>[FR] PROCÉDÉ DE PREPARATION DE DÉRIVÉS D'ALKYLIDÈNECYCLOPENTANONE
    申请人:FIRMENICH & CIE
    公开号:WO2004043895A1
    公开(公告)日:2004-05-27
    The present invention relates to the field of organic synthesis and more particularly to a new process for the preparation of a compound of formula (I), in the form of any one of its isomers or a mixture thereof, Formula (I) wherein, more preferably, G represents a C=O group, R1 represents a butyl group and R2 represents a methyl group. The process of the invention involves an 2-(1-hydroxyalkyl)-cyclopent-2-en-1-one derivative, as starting material, which can be then converted into a compound of formula (I) by a process comprising a thermal rearrangement. The 2-alkylidene-3-oxo-cyclopentylacetate derivative and the 2-(1-hydroxyalkyl)-cyclopent-2-en-1-one derivative are also an object of the invention.
    本发明涉及有机合成领域,更具体地涉及一种制备化合物(I)的新工艺,其形式为其任一异构体或其混合物,其中,更优选地,G代表C=O基团,R1代表丁基基团,R2代表甲基基团。该发明的工艺涉及以2-(1-羟基烷基)-环戊-2-烯-1-酮衍生物作为起始材料,该衍生物可以通过热重排的过程转化为化合物(I)。2-烷基亚甲基-3-氧代-环戊基乙酸酯衍生物和2-(1-羟基烷基)-环戊-2-烯-1-酮衍生物也是本发明的对象。
  • Efficient routes to cyclic 2,3-epoxyalcohols from cycloalkenyl ketones, via cycloalkenyl alcohols
    作者:Charles M. Marson、Andrew J. Walker、Jane Pickering、Steven Harper、Roger Wrigglesworth、Simon J. Edge
    DOI:10.1016/s0040-4020(01)80560-3
    日期:1993.1
    The minimising of torsional strain and non-bonding interactions is proposed as the explanation of high diastereoselectivity observed in the epoxidation of cycloalkenyl alcohols. reported for twenty three examples. The resulting 2,3-epoxyalcohols are key intermediates in the synthesis of tricyclic 1, 2-diols and beta-hydroxy ketones
  • 383. Studies in molecular rearrangement. Part VI. Syntheses and oxotropic rearrangements in the cyclopentenyl series
    作者:E. A. Braude、W. F. Forbes
    DOI:10.1039/jr9510001755
    日期:——
  • A PROCESS FOR THE PREPARATION OF ALKYLIDENECYCLOPENTANONE DERIVATIVES
    申请人:FIRMENICH SA
    公开号:EP1562888A1
    公开(公告)日:2005-08-17
  • METHOD OF USING ORGANIC COMPOUNDS
    申请人:Givaudan SA
    公开号:EP2046147A1
    公开(公告)日:2009-04-15
查看更多