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12-hydroxyoctadecanoic acid vinyl ester | 152752-18-6

中文名称
——
中文别名
——
英文名称
12-hydroxyoctadecanoic acid vinyl ester
英文别名
Vinyl 12-hydroxystearate;ethenyl 12-hydroxyoctadecanoate
12-hydroxyoctadecanoic acid vinyl ester化学式
CAS
152752-18-6
化学式
C20H38O3
mdl
——
分子量
326.52
InChiKey
DAUXBFDFCKRQAW-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):
    7.1
  • 重原子数:
    23
  • 可旋转键数:
    18
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.85
  • 拓扑面积:
    46.5
  • 氢给体数:
    1
  • 氢受体数:
    3

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    12-hydroxyoctadecanoic acid vinyl ester 在 4 A molecular sieve 作用下, 以 正己烷 为溶剂, 反应 26.0h, 生成 13,26-dihexyl-1,14-dioxacyclohexacosane-2,15-dione
    参考文献:
    名称:
    Lipase catalyzed formation of lactones via irreversible intramolecular acyltransfer
    摘要:
    The lipase catalyzed formation of lactones is greatly facilitated, if the conditions of irreversible acyltransfer are employed. While only insignificant amounts of lactones are obtained from hydroxy carboxylic acids (+/-)-1a-f or their methyl esters (+/-)-2a-f, considerable yields can be obtained, if the corresponding vinyl esters (+/-)-3a-f are used as substrates. Due to the enantioselectivities, displayed by the lipase from Pseudomonas sp., optically active products are formed.
    DOI:
    10.1016/s0957-4166(00)80147-0
  • 作为产物:
    描述:
    乙酸乙烯酯12-羟基硬脂酸 在 palladium diacetate 氢氧化钾 作用下, 反应 24.0h, 以83%的产率得到12-hydroxyoctadecanoic acid vinyl ester
    参考文献:
    名称:
    Synthesis of Hydroxycarboxylic Acid Vinyl Esters
    摘要:
    在醋酸乙烯酯和醋酸钯(II)作为催化剂存在的基本条件下,成功地将具有伯羟基或仲羟基官能团的羟基羧酸转化为相应的乙烯基酯。对以前经常干扰这些转化的副反应进行了研究,并对反应条件进行了优化,以达到最高的产品产率。
    DOI:
    10.1055/s-1994-25479
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文献信息

  • Vinyl chloride resin compositions, moulded products obtained therefrom, and methods of producing the compositions and molded products
    申请人:Chisso Corporation
    公开号:EP0635530A1
    公开(公告)日:1995-01-25
    A vinyl chloride resin composition comprises (a) 100 parts by weight of a crosslinkable vinyl chloride resin, or 100 parts by weight in total of 1 to 99 parts by weight of a crosslinkable vinyl chloride resin and 99 to 1 part by weight of a vinyl chloride resin; (b) 1 to 100 parts by weight of a polyol compound; and (c) as a crosslinking agent, 1 to 100 parts by weight of a blocked polyisocyanate compound.
    氯乙烯树脂组合物包括 (a) 100 份(重量)可交联氯乙烯树脂,或 1 至 99 份(重量)可交联氯乙烯树脂和 99 至 1 份(重量)氯乙烯树脂共 100 份(重量); (b) 1 至 100 份(重量份數)多元醇化合物;及 (c) 1 至 100 份(重量)封端多异氰酸酯化合物作为交联剂。
  • Vinyl chloride resin composition
    申请人:CHISSO CORPORATION
    公开号:EP0473426B1
    公开(公告)日:1996-10-16
  • US5242965A
    申请人:——
    公开号:US5242965A
    公开(公告)日:1993-09-07
  • Synthesis of Hydroxycarboxylic Acid Vinyl Esters
    作者:Mario Lobell、Manfred P. Schneider
    DOI:10.1055/s-1994-25479
    日期:——
    The conversion of hydroxycarboxylic acids with primary or secondary hydroxy functions into the corresponding vinyl esters was successfully achieved under basic conditions in presence of vinyl acetate and palladium(II) acetate as catalyst. Side reactions, which were previously frequently interfering with these transformations, have been studied and reaction conditions optimised to reach maximum product yield.
    在醋酸乙烯酯和醋酸钯(II)作为催化剂存在的基本条件下,成功地将具有伯羟基或仲羟基官能团的羟基羧酸转化为相应的乙烯基酯。对以前经常干扰这些转化的副反应进行了研究,并对反应条件进行了优化,以达到最高的产品产率。
  • Lipase catalyzed formation of lactones via irreversible intramolecular acyltransfer
    作者:Mario Lobell、Manfred P. Schneider
    DOI:10.1016/s0957-4166(00)80147-0
    日期:1993.5
    The lipase catalyzed formation of lactones is greatly facilitated, if the conditions of irreversible acyltransfer are employed. While only insignificant amounts of lactones are obtained from hydroxy carboxylic acids (+/-)-1a-f or their methyl esters (+/-)-2a-f, considerable yields can be obtained, if the corresponding vinyl esters (+/-)-3a-f are used as substrates. Due to the enantioselectivities, displayed by the lipase from Pseudomonas sp., optically active products are formed.
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