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4-Methyl-2-methylene-cyclopentanone | 143159-21-1

中文名称
——
中文别名
——
英文名称
4-Methyl-2-methylene-cyclopentanone
英文别名
4-Methyl-2-methylidenecyclopentan-1-one
4-Methyl-2-methylene-cyclopentanone化学式
CAS
143159-21-1
化学式
C7H10O
mdl
——
分子量
110.156
InChiKey
BGSOOWQVJDSYOU-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:
    8
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为产物:
    描述:
    (4E)-2-(trimethylsilylmethyl)hexa-1,4-dien-3-one三氯化铁 作用下, 以 二氯甲烷 为溶剂, 反应 2.0h, 以58%的产率得到4-Methyl-2-methylene-cyclopentanone
    参考文献:
    名称:
    Synthesis of α-methylenecyclopentanones via silicon directed nazarov reaction of α-trimethylsilymethyl substituted divinyl ketones.
    摘要:
    Reactions of alpha-trimethylsilylmethyl-substituted divinyl ketones with FeCl3 gave alpha-methylenecyclopentanones. Thienyl and N-methylpyrrolyl (alpha-trimethylsilylmethyl)vinyl ketones also underwent cyclization to afford the corresponding alpha-methylenecyclopentanones.
    DOI:
    10.1016/s0040-4039(00)92672-8
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文献信息

  • Thiophosphates and Selenophosphates in Organic Synthesis. A New Approach to Exocyclic Olefins and Bicyclic Enones
    作者:Aleksandra Skowronska、Ewa Krawczyk、Marek Koprowski、Piotr Dybowski
    DOI:10.1080/10426509608046285
    日期:1996.2.1
  • ALIGNMENT COMPOSITION, LIQUID CRYSTAL DISPLAY PANEL AND METHOD OF MANUFACTURING SAME
    申请人:Samsung Display Co., Ltd.
    公开号:EP3002324B1
    公开(公告)日:2019-04-03
  • RING-OPENING POLYMERIZATION METHODS AND RECYCLABLE BIORENEWABLE POLYESTERS
    申请人:Colorado State University Research Foundation
    公开号:US20180118880A1
    公开(公告)日:2018-05-03
    The invention provides polymers of Formulas I-III, such as polyesters and unsaturated polyesters, and crosslinked and copolymerized polymers thereof. The invention also provides methods to catalytically ring-open five-membered rings such lactones, lactams, and thiolactones, as via ring-opening polymerization. The polymerization products are recyclable and can be depolymerized back to their monomer form via thermolysis and acid or base catalysis.
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