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dec-9-en-1-yl acrylate | 136772-31-1

中文名称
——
中文别名
——
英文名称
dec-9-en-1-yl acrylate
英文别名
10-Undecenyl acrylate, contains <1000 ppm MEHQ as inhibitor, 98%;dec-9-enyl prop-2-enoate
dec-9-en-1-yl acrylate化学式
CAS
136772-31-1
化学式
C13H22O2
mdl
——
分子量
210.316
InChiKey
WDGPKCJWRJSYLS-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:
    280.3±19.0 °C(Predicted)
  • 密度:
    0.888±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.7
  • 重原子数:
    15
  • 可旋转键数:
    11
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.62
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

上下游信息

  • 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:
    dec-9-en-1-yl acrylate甲基三辛基氯化铵 sodium hydroxide 、 sodium tungstate 、 双氧水 作用下, 以 二氯甲烷磷酸 为溶剂, 反应 20.0h, 以68%的产率得到2-propenoic acid, 8-oxiranyloctyl ester
    参考文献:
    名称:
    H 2 O 2 -Na 2 WO 4体系在相转移催化下通过不饱和(甲基)丙烯酸酯的选择性环氧化合成环氧(甲基)丙烯酸酯。
    摘要:
    研究了各种经典的环氧化剂对不饱和(甲基)丙烯酸酯的选择性环氧化。结果表明,在相转移催化下,通过使用H 2 O 2(20%)-Na 2 WO 4体系可以得到高选择性和高收率。在这些条件下,严格控制温度和初始pH值可防止在这些选择性环氧化过程中发生聚合。结果表明,环氧化的选择性取决于两个双键亲核性的差异。
    DOI:
    10.1016/s0040-4020(01)90120-6
  • 作为产物:
    描述:
    9-十烯-1-醇丙烯酰氯4-二甲氨基吡啶2,6-二叔丁基-4-甲基苯酚三乙胺 作用下, 以 四氢呋喃 为溶剂, 反应 2.0h, 以73%的产率得到dec-9-en-1-yl acrylate
    参考文献:
    名称:
    Hyperbranched Macromolecules via Olefin Metathesis
    摘要:
    A facile route to hyperbranched polymers via acyclic diene metathesis is reported. Any molecule functionalized with two or more acrylate groups and one terminal olefin can serve as an AB, monomer when exposed to an imidazolinylidene-based ruthenium olefin metathesis catalyst, due to the cross metathesis selectivity of this catalyst. For the polymers obtained by this method, both H-1 NMR spectroscopy and triple detector size exclusion chromatography conclusively indicate a branched architecture.
    DOI:
    10.1021/ja0759040
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文献信息

  • Preparation of Organosilicon Compound Having (Meth)acryloyloxy Group
    申请人:Shin-Etsu Chemical Co., Ltd.
    公开号:US20210139515A1
    公开(公告)日:2021-05-13
    A (meth)acryloyloxy-containing organosilicon compound (3) is prepared by simultaneously feeding a hydrohalosilane compound (1) and a (meth)acrylate compound (2) in the presence of a polymerization inhibitor to a reaction system, and effecting hydrosilylation reaction in the presence of a platinum catalyst. The content of (meth)acrylate compound (2) is 0-100 mol % based on the content of organosilicon compound (3) in the reaction system. R is a C 1 -C 10 monovalent hydrocarbon group, X is halogen, n is 1, 2 or 3, R 2 is H or methyl, and R 3 is a C 1 -C 18 alkylene group.
    通过在聚合抑制剂的存在下同时加入羟卤代硅烷化合物(1)和(甲基)丙烯酸酯化合物(2)到反应体系中,利用铂催化剂进行氢硅烷化反应,制备含有(甲基)丙烯酰氧基的有机硅化合物(3)。在反应体系中,(甲基)丙烯酸酯化合物(2)的含量基于有机硅化合物(3)的含量为0-100摩尔%。其中,R是C1-C10一价烃基,X是卤素,n为1、2或3,R2为氢或甲基,R3为C1-C18烷基。
  • Electrochemical Azidocyanation of Alkenes
    作者:Yun‐Tao Zheng、Hai‐Chao Xu
    DOI:10.1002/anie.202313273
    日期:2024.2.5
    An electrochemical alkene azidocyanation reaction that is compatible with both alkyl and aryl alkenes was developed. The reactions involving aryl alkenes could be obtained with good enantioselectivities by employing a chiral ligand. Notably, this method of alkene difunctionalization employs readily accessible reagents and is distinguished by its demonstrated functional group tolerance.
    开发了一种与烷基和芳基烯烃均相容的电化学烯烃叠氮氰化反应。通过使用手性配体,涉及芳基烯烃的反应可以具有良好的对映选择性。值得注意的是,这种烯烃双官能化方法采用易于获得的试剂,并以其经证明的官能团耐受性而著称。
  • Chiral Cp<sup>x</sup>Rhodium(III)‐Catalyzed Enantioselective Aziridination of Unactivated Terminal Alkenes
    作者:Juanjuan Wang、Mu‐Peng Luo、Yi‐Jie Gu、Yu‐Ying Liu、Qin Yin、Shou‐Guo Wang
    DOI:10.1002/anie.202400502
    日期:2024.3.18
    A chiral cyclopentadienyl-rhodium(III) catalyzed highly enantioselective aziridination of challenging unactivated terminal alkenes and N-pivalolyloxy sulfonamides has been developed. This catalytic system demonstrated outstanding catalytic activity and broad functional group tolerance, yielding synthetically important and highly valuable chiral aziridines with good to excellent yields and enantioselectivities
    开发了一种手性环戊二烯基铑 (III) 催化的具有挑战性的未活化末端烯烃和N-新戊酰氧基磺酰胺的高度对映选择性氮丙啶化反应。该催化体系表现出出色的催化活性和广泛的官能团耐受性,产生具有合成重要性和高价值的手性氮丙啶,具有良好至优异的产率和对映选择性(高达 99% 的产率,93% ee)。
  • Ink composition, ink jet recording method, method for producing planographic printing plate, and planographic printing plate
    申请人:FUJIFILM Corporation
    公开号:EP2169020A1
    公开(公告)日:2010-03-31
    The invention provides an ink composition comprising a polymerization initiator, a (meth)acrylate having a double bond with a carbon atom having an sp3 hybrid orbital at an α position, and a colorant; an ink jet recording method using the ink composition; a planographic printing plate obtained by using the ink composition; and a method for producing the planographic printing plate.
    本发明提供了一种油墨组合物,该组合物包含聚合引发剂、具有双键的(甲基)丙烯酸酯(其碳原子在 α 位置具有 sp3 杂化轨道)和着色剂;使用该油墨组合物的喷墨记录方法;使用该油墨组合物获得的平版印刷板;以及生产该平版印刷板的方法。
  • PREPARATION OF ORGANOSILICON COMPOUND HAVING (METH)ACRYLOYLOXY GROUP
    申请人:Shin-Etsu Chemical Co., Ltd.
    公开号:EP3819301A1
    公开(公告)日:2021-05-12
    A (meth)acryloyloxy-containing organosilicon compound (3) is prepared by simultaneously feeding a hydrohalosilane compound (1) and a (meth)acrylate compound (2) in the presence of a polymerization inhibitor to a reaction system, and effecting hydrosilylation reaction in the presence of a platinum catalyst. The content of (meth)acrylate compound (2) is 0-100 mol% based on the content of organosilicon compound (3) in the reaction system. R1 is a C1-C10 monovalent hydrocarbon group, X is halogen, n is 1, 2 or 3, R2 is H or methyl, and R3 is a C1-C18 alkylene group.
    在聚合抑制剂存在下,将氢卤硅烷化合物(1)和(甲基)丙烯酸酯化合物(2)同时加入反应体系,并在铂催化剂存在下进行氢化硅反应,制备含(甲基)丙烯酰氧基的有机硅化合物(3)。根据反应体系中有机硅化合物(3)的含量,(甲基)丙烯酸酯化合物(2)的含量为 0-100 摩尔%。R1 是 C1-C10 单价烃基,X 是卤素,n 是 1、2 或 3,R2 是 H 或甲基,R3 是 C1-C18 亚烷基。
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