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4-oxaoctanoyl chloride | 4244-62-6

中文名称
——
中文别名
——
英文名称
4-oxaoctanoyl chloride
英文别名
β-n-Butoxypropionylchlorid;3-butoxy-propionyl chloride;3-Butyloxy-propionylchlorid;3-Butoxypropanoyl chloride
4-oxaoctanoyl chloride化学式
CAS
4244-62-6
化学式
C7H13ClO2
mdl
——
分子量
164.632
InChiKey
GUMULBYTTAQVAO-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:
    86 °C(Press: 20 Torr)
  • 密度:
    1.0157 g/cm3

计算性质

  • 辛醇/水分配系数(LogP):
    1.8
  • 重原子数:
    10
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.86
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    4-oxaoctanoyl chloride 生成 3-butoxy-1-phenyl-1-propanone
    参考文献:
    名称:
    Synthesis of Certain 2-Alkoxyethyl Phenyl Ketones
    摘要:
    DOI:
    10.1021/ja01178a065
  • 作为产物:
    描述:
    参考文献:
    名称:
    Effect of heteroatoms in the side chains of disklike molecules on the formation of discotic liquid crystalline phases
    摘要:
    Incorportion of oxygen and sulfur atoms into the side chains of discotic liquid crystals generally results in a depression of both the crystal to discotic and discotic to isotropic transition temperatures relative to the n-alkyl analogue. In contrast, replacement of the methylenes in side-chain positions 4 of 2,3,6,7,10,11-hexakis(alkanoyloxy)triphenylenes increases the clearing (M-I) temperature from 120 to 200-degrees-C. This effect is specific for sulfur substitution, to the triphenylene series, and to the 4-position. It is not expected, based on a simple model for discotic-phase formation.
    DOI:
    10.1021/jo00021a020
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文献信息

  • Nasarow et al., Zhurnal Obshchei Khimii, 1956, vol. 26, p. 2798,2802,3157,3159; engl.Ausg.3117,3121,3521,3523
    作者:Nasarow et al.
    DOI:——
    日期:——
  • Liquid crystals. 1. .beta.-Oxygen effect on stabilization of hexakis(acyloxy)benzene mesophase
    作者:Iwao Tabushi、Kazuo Yamamura、Yukihiro Okada
    DOI:10.1021/jo00388a029
    日期:1987.6
  • Terent'ew et al., Zhurnal Obshchei Khimii, 1956, vol. 26, p. 719,722; engl.Ausg.S.827,829
    作者:Terent'ew et al.
    DOI:——
    日期:——
  • Fluorocarbon acids and derivatives
    申请人:MINNESOTA MINING &
    公开号:US02713593A1
    公开(公告)日:1955-07-19
  • SYNTHESIS OF SUBSTITUTED SALICYLALDEHYDE DERIVATIVES
    申请人:Farmer Jay J.
    公开号:US20130197223A1
    公开(公告)日:2013-08-01
    Among other things, the present invention encompasses methods of synthesizing salicylaldehyde derivatives comprising the steps of: a) providing salicylaldehyde or a derivative thereof, b) forming an anhydro dimer of the provided salicylaldehyde compound, c) performing one or more chemical transformations on the anhydro dimer and d) hydrolyzing the anhydro dimer to provide a salicylaldehyde derivative different from that provided in step (a).
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