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(E)-1-iodoundecene | 66142-64-1

中文名称
——
中文别名
——
英文名称
(E)-1-iodoundecene
英文别名
(E)-1-iodoundec-1-ene
(E)-1-iodoundecene化学式
CAS
66142-64-1
化学式
C11H21I
mdl
——
分子量
280.192
InChiKey
SHBJGEGCCXEOIZ-ZHACJKMWSA-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):
    6.2
  • 重原子数:
    12
  • 可旋转键数:
    8
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.82
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

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文献信息

  • A General Method for the Synthesis of Nonracemic <i>trans</i>-Epoxides:  Concise Syntheses of <i>trans</i>-Epoxide-Containing Insect Sex Pheromones
    作者:Baldip Kang、Robert Britton
    DOI:10.1021/ol702273n
    日期:2007.11.1
    developed that provides rapid access to alkyl-, alkenyl-, alkynyl-, and phenyl-substituted trans-epoxides from aldehydes. This methodology has also been applied in concise and high-yielding syntheses of both trans-epoxide containing insect sex pheromones.
    已经开发了用于合成手性非外消旋反式环氧化物的通用方法,该方法提供了从醛类快速进入烷基,烯基,炔基和苯基取代的反式环氧化物的途径。该方法也已用于含有反式环氧化物的昆虫性信息素的简明和高产合成中。
  • Ruthenium‐Catalyzed Synthesis of Aryl and Alkenyl Halides from Fluorosulfonates
    作者:Clotilde Plaçais、Sherif J. Kaldas、Morgan Donnard、Armen Panossian、David Bernier、Sergii Pazenok、Frédéric R. Leroux
    DOI:10.1002/chem.202301420
    日期:2023.7.20
    coupling reactions has increased over the past decade. Surprisingly, the use and synthesis of alkenyl fluorosulfonates is still poorly described. In this paper, the advantageous use of aryl and alkenyl fluorosulfonates instead of the corresponding triflates is reported to synthesize aryl and alkenyl halides using halide salts and commercially available ruthenium catalysts.
    在过去的十年中,氟磺酸芳基酯在偶联反应中的相关性有所增加。令人惊讶的是,对烯基氟磺酸盐的使用和合成仍然知之甚少。在本文中,报道了使用芳基和链烯基氟磺酸盐代替相应的三氟甲磺酸盐,利用卤化物盐和市售催化剂合成芳基和链烯基卤化物。
  • A Strategy for the Late-Stage Divergent Syntheses of Scyphostatin Analogues
    作者:Jacob Y. Cha、G. Leslie Burnett、Yaodong Huang、Jarrod B. Davidson、Thomas R. R. Pettus
    DOI:10.1021/jo102327e
    日期:2011.3.4
    This account details the synthesis of two scyphostatin analogues exhibiting a reactive polar epoxycyclohexenone core and various amide side chains outfitted for late-stage chemical derivatization into the desirable lipophilic tails. Our efforts highlight a key ipso-dearomatization process and provide new insights regarding the incompatibility and orthogonal reactivity of scyphostatin's functional groups. We further showcase the utility of resorcinol derived 2,5-cyclohexadienones as synthetic platforms capable of participating in selective chemical reactivity, and we further demonstrate their potential for rapid elaboration into complex structural motifs,
  • BESTMANN, HANS JURGEN;RIPPEL, HANS CHRISTOPH;DOSTALEK, ROMAN, TETRAHEDRON LETT., 30,(1989) N9, C. 5261-5262
    作者:BESTMANN, HANS JURGEN、RIPPEL, HANS CHRISTOPH、DOSTALEK, ROMAN
    DOI:——
    日期:——
  • FLUOROALKYLATED AMPHIPHILIC LIGANDS, THEIR METALLIC COMPLEXES AND THEIR USES
    申请人:S.A. A.T.T.A. APPLICATIONS ET TRANSFERTS DE TECHNOLOGIES AVANCEES
    公开号:EP0606308A1
    公开(公告)日:1994-07-20
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