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bis-(2-ethylcarbonate)ethyl sulfide | 500798-11-8

中文名称
——
中文别名
——
英文名称
bis-(2-ethylcarbonate)ethyl sulfide
英文别名
2-(2-Ethoxycarbonyloxyethylsulfanyl)ethyl ethyl carbonate
bis-(2-ethylcarbonate)ethyl sulfide化学式
CAS
500798-11-8
化学式
C10H18O6S
mdl
——
分子量
266.315
InChiKey
VVSCRDVFQXBWEN-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):
    2.2
  • 重原子数:
    17
  • 可旋转键数:
    12
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.8
  • 拓扑面积:
    96.4
  • 氢给体数:
    0
  • 氢受体数:
    7

反应信息

  • 作为反应物:
    描述:
    bis-(2-ethylcarbonate)ethyl sulfide4-羟基苯甲腈 以 neat (no solvent) 为溶剂, 反应 24.0h, 生成 1,5-bis(4-cyanophenoxy)-3-thiapentane
    参考文献:
    名称:
    Behaviour of iprit carbonate analogues in solventless reactions
    摘要:
    硫代碳酸硫酯类似物在常压下,在无溶剂条件下,存在或不存在催化剂量的碱的情况下,与多种底物发生亲核取代反应。
    DOI:
    10.1039/c4ra03254c
  • 作为产物:
    描述:
    硫二甘醇碳酸二乙酯 反应 17.0h, 以90%的产率得到bis-(2-ethylcarbonate)ethyl sulfide
    参考文献:
    名称:
    Behaviour of iprit carbonate analogues in solventless reactions
    摘要:
    硫代碳酸硫酯类似物在常压下,在无溶剂条件下,存在或不存在催化剂量的碱的情况下,与多种底物发生亲核取代反应。
    DOI:
    10.1039/c4ra03254c
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文献信息

  • PROCESS FOR PREPARING A POLYMER FROM MUSTARD CARBONATE ANALOGUES
    申请人:Tundo, Pietro Rosario
    公开号:EP3642259A1
    公开(公告)日:2020-04-29
  • [EN] PROCESS FOR PREPARING A POLYMER FROM MUSTARD CARBONATE ANALOGUES<br/>[FR] PROCÉDÉ DE PRÉPARATION D'UN POLYMÈRE À PARTIR D'ANALOGUES CARBONATES DE MOUTARDE
    申请人:TUNDO PIETRO ROSARIO
    公开号:WO2018235046A1
    公开(公告)日:2018-12-27
    The present invention relates to a process for preparing a polymer that comprises at least a step of carrying out a mass polymerization of a reaction mixture comprising at least one mustard carbonate analogue of general formula R1OOCO-R2-Z-R3-OCOOR4 (I) and at least one hydroxy-subst ituted aromatic compound of general formula Ar(OH)n (II), wherein in said general formulas: R1 and R4, equal or different, are linear or branched C1-C6 alkyl; R2 and R3, equal or different, are a linear or branched C2 -C4 alkylene, preferably ethylene; Z is a radical selected from: S; N-Y, wherein Y is selected from: hydrogen, linear or branched C1-C6 alkyl, or a radical -R6OCOOR5 where R6 is a linear or branched C2 -C4 alkyl and R5 is a linear or branched C1-C6 alkyl; Ar is an aromatic radical selected from: benzene, naphthalene, phenanthrene, anthracene, biaryl radical or two or more aromatic radicals bridged by a linear or branched C1-C10 alkylene group, said Ar group being optionally substituted; n is an integer from 2 to 5. The present invention further relates to the polymer obtainable with the aforesaid process.
  • Behaviour of iprit carbonate analogues in solventless reactions
    作者:F. Arico'、S. Evaristo、P. Tundo
    DOI:10.1039/c4ra03254c
    日期:——

    Sulfur iprit carbonate analogues showed to undergo nucleophilic substitution with several substrates in neat conditions at atmospheric pressure, in the presence and in the absence of a catalytic amount of base.

    硫代碳酸硫酯类似物在常压下,在无溶剂条件下,存在或不存在催化剂量的碱的情况下,与多种底物发生亲核取代反应。
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