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(2-Ethyl-but-1-enylidene)-isopropyl-amine | 66102-43-0

中文名称
——
中文别名
——
英文名称
(2-Ethyl-but-1-enylidene)-isopropyl-amine
英文别名
——
(2-Ethyl-but-1-enylidene)-isopropyl-amine化学式
CAS
66102-43-0
化学式
C9H17N
mdl
——
分子量
139.241
InChiKey
FTSVAGPRKGHGGZ-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):
    3.4
  • 重原子数:
    10
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.78
  • 拓扑面积:
    12.4
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

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文献信息

  • Chemiluminescence of imino-1,2-dioxetan formed from ketenimine and singlet oxygen
    作者:Yoshikatsu Ito、Hiroaki Yokoya、Kazuaki Kyono、Soichiro Yamamura、Yutaka Yamada、Teruo Matsuura
    DOI:10.1039/c39800000898
    日期:——
    The chemiluminescent properties of several imino-1,2-dioxetans prepared by the photosensitized oxygenation of ketenimines at –78 °C, indicate that the energy level of the transition state for their decompostion to the corresponding ketones and isocyanates is low and that the decomposition proceeds via a biradical mechanism.
    通过在–78°C下对酮亚胺的光敏氧化制备的几种亚氨基1,2-二氧杂环丁烷的化学发光性质表明,它们分解为相应的酮和异氰酸酯的过渡态能级很低,并且分解会继续进行通过双自由基机制。
  • Preparation of thionamide compounds by sulfuration of imines
    申请人:ASHLAND OIL, INC.
    公开号:EP0083901A1
    公开(公告)日:1983-07-20
    Useful thionamide compounds are prepared by reacting sulfur with imines of the structural formula: where R is an alkyl group of 1 to 18 carbon atoms and is other than a phenyl or cyclohexyl group, R1 and R2 are phenyl groups or alkyl groups of 1 to 18 carbon atoms, and R3 is a phenyl group or is hydrogen, in the presence of a diol or triol compound. The total number of carbons in R, R1, R2, and R3 does not exceed 36 in number.
    有用的硫代酰胺化合物是在二元醇或三元醇化合物存在下,通过硫与结构式如下的亚胺反应制备的: 其中 R 是 1 至 18 个碳原子的烷基,但不是苯基或环己基,R1 和 R2 是苯基或 1 至 18 个碳原子的烷基,R3 是苯基或氢。 R、R1、R2 和 R3 中的碳原子总数不超过 36 个。
  • Regiospecific synthesis of α-chloro- and α-fluoro-1,2-diones
    作者:Riccardo Surmont、Bart De Corte、Norbert De Kimpe
    DOI:10.1016/j.tetlet.2009.04.049
    日期:2009.7
    alpha-Chloro-1,2-diones and alpha-fluoro-1,2-diones were prepared from the corresponding alpha-chloroaldimines by a sequence of reactions involving cyanation to alpha-cyanoenamines, alpha-halogenation to form alpha-chloro-or alpha-fluoroimidoyl cyanides and addition of organolithium reagents across the nitrile moiety, followed by acidic hydrolysis. All steps are straightforward and occur without side reactions finally leading to regiospecifically chlorinated and fluorinated 1,2-diones in good yields. (c) 2009 Elsevier Ltd. All rights reserved.
  • DE, KIMPE, N.;VERHE, R.;DE, BUYCK, L.;SCHAMP, N., ORG. PREP. AND PROCED. INT., 1982, 14, N 3, 213-215
    作者:DE, KIMPE, N.、VERHE, R.、DE, BUYCK, L.、SCHAMP, N.
    DOI:——
    日期:——
  • US4348523A
    申请人:——
    公开号:US4348523A
    公开(公告)日:1982-09-07
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