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1-氯-4-辛炔 | 51575-84-9

中文名称
1-氯-4-辛炔
中文别名
——
英文名称
1-chloro-4-octyne
英文别名
1-chlorooct-4-yne
1-氯-4-辛炔化学式
CAS
51575-84-9
化学式
C8H13Cl
mdl
MFCD00041553
分子量
144.644
InChiKey
JLMMBXPBVPCUJA-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:
    87°C 23mm
  • 密度:
    0,932 g/cm3

计算性质

  • 辛醇/水分配系数(LogP):
    3.2
  • 重原子数:
    9
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

安全信息

  • 海关编码:
    2903299090

SDS

SDS:094b2745c6255a9bff4cae65d8cc354e
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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:
    1-氯-4-辛炔tris(acetonitrile)pentamethylcyclopentadienylruthenium(II) hexafluorophosphate 三乙氧基硅烷copper(l) iodide四丁基氟化铵 作用下, 以 二氯甲烷四氢呋喃 为溶剂, 反应 0.5h, 以59%的产率得到trans-1-Chlor-octen-(4)
    参考文献:
    名称:
    A Chemoselective Reduction of Alkynes to (E)-Alkenes
    摘要:
    The trans reduction of all types of alkynes to give (E)-olefins is achieved through a two-stage trans hydrosilylation and protodesilylation. Reaction of an alkyne and a silane with the ruthenium catalyst [Cp*Ru(MeCN)3]PF6 results in clean hydrosilylation to give only the (Z)-trans addition product at ambient temperature with catalyst loadings of 1-5 mol %. The crude vinylsilane products are then protodesilylated by the action of cuprous iodide and TBAF at rt-35 degrees C. The reaction is compatible with many sensitive functional groups and provides a general trans-alkyne reduction not possible by other means.
    DOI:
    10.1021/ja026457l
  • 作为产物:
    描述:
    参考文献:
    名称:
    THE ISOMERIC NORMAL NONYNOIC ACIDS
    摘要:
    DOI:
    10.1021/jo01375a004
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文献信息

  • Silver halide photographic material
    申请人:FUJI PHOTO FILM CO., LTD.
    公开号:EP0458278A1
    公开(公告)日:1991-11-27
    A silver halide photographic material low in fogging generation and high in sensitivity comprising a silver halide emulsion selenium sensitized with at least one compound selected from the group consisting of compounds represented by general formulae (I) and (III): wherein each of R₁, R₂, R₃ and R₄ represents an alkyl group, a cycloalkyl group, an alkenyl group, an alkynyl group, an aralkyl group, an aryl group, a heterocyclic group, an acyl group, a carboxyl group, an alkoxycarbonyl group, an aryloxycarbonyl group, a carbamoyl group or a sulfamoyl group, provided that a tetramethylselenourea is excluded; wherein each of R₈, R₉, R₁₀ and R₁₁ represents a hydrogen atom, an alkyl group, a cycloalkyl group, an alkenyl group, an alkynyl group, an aralkyl group, an aryl group, a heterocyclic group, an acyl group, a carboxyl group, a formyl group, an alkoxycarbonyl group, an aryloxycarbonyl group, a carbamoyl group or a sulfamoyl group, provided that at least one pair of R₈ and R₉, R₉ and R₁₀, R₁₀ and R₁₁, and R₁₁ and R₈ combine to form a ring.
    一种卤化银感光材料,具有低雾度和高感光度的特点,它包括一种用至少一种从通式 (I) 和 (III) 所代表的化合物组成的组中选出的化合物感光的卤化银乳剂硒: 其中 R₁、R₂、R₃ 和 R₄ 各自代表烷基、环烷基、烯基、炔基、芳基、芳基、杂环基、酰基、羧基、烷氧羰基、芳氧羰基、氨基甲酰基或氨基磺酰基,但不包括四甲基硒脲; 其中 R₈、R₉、R₁₀ 和 R₁₁ 各代表氢原子、烷基、环烷基、烯基、炔基、芳烷基、芳基、杂环基、酰基、羧基甲酰基、烷氧羰基、芳氧羰基、氨基甲酰基或氨基磺酰基、但至少有一对 R₈ 和 R₉、R₉ 和 R₁₀、R₁₀ 和 R₁₁ 以及 R₁₁ 和 R₈ 结合形成一个环。
  • Vasil'ev, A. A.; Cherkaev, G. V.; Nikitina, M. A., Russian Journal of Organic Chemistry, 1993, vol. 29, # 5.1, p. 735 - 739
    作者:Vasil'ev, A. A.、Cherkaev, G. V.、Nikitina, M. A.
    DOI:——
    日期:——
  • Seidel, Wolfgang; Schaefer, Hans J., Chemische Berichte, 1980, vol. 113, # 12, p. 3898 - 3903
    作者:Seidel, Wolfgang、Schaefer, Hans J.
    DOI:——
    日期:——
  • Zakharkin, L. I.; Anikina, E. V., Journal of Organic Chemistry USSR (English Translation), 1986, vol. 22, # 12, p. 2217 - 2221
    作者:Zakharkin, L. I.、Anikina, E. V.
    DOI:——
    日期:——
  • Long-acting contraceptive agents: Norethisterone esters of monoalkenyl and monoalkynyl acids
    作者:Cosme G. Francisco、Raimundo Freire、Rosendo Hernandez、Jose A. Salazar、Ernesto Suarez、Gustavo A. Garcia De La Mora、Jose A.Noguez A.、Alejandrina Acosta H.、Oswaldo Jimeno
    DOI:10.1016/0039-128x(83)90097-1
    日期:1983.3
    The synthesis of nine new esters of norethisterone (17 alpha-ethynyl-17 beta-hydroxyestr-4-en-3-one) is described, with the esterifying acids bearing an acetylenic or olefinic function in a chain of eight or nine carbon atoms, for evaluation as long-acting contraceptive agents.
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