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2-异丙基-1-戊烯 | 16746-02-4

中文名称
2-异丙基-1-戊烯
中文别名
——
英文名称
2-(1-methylethyl)-1-pentene
英文别名
2-isopropyl-1-pentene;2-isopropylpentene;2-isopropyl-pent-1-ene;3-Methyl-2-propyl-but-1-en;2-Isopropyl-pent-1-en;2-methyl-3-methylene-hexane;1-Pentene, 2-(1-methylethyl);2-methyl-3-methylidenehexane
2-异丙基-1-戊烯化学式
CAS
16746-02-4
化学式
C8H16
mdl
MFCD00060998
分子量
112.215
InChiKey
QOUCFWFZPKWYRE-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

  • 熔点:
    -103.01°C (estimate)
  • 沸点:
    120.2°C (estimate)
  • 密度:
    0.7210
  • 保留指数:
    753.7;754;750

计算性质

  • 辛醇/水分配系数(LogP):
    3.8
  • 重原子数:
    8
  • 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

SDS

SDS:b0fe6bb4b0b947621e5546a0151a055e
查看

反应信息

  • 作为反应物:
    描述:
    2-异丙基-1-戊烯sodium hypophosphite二叔丁基过氧化物溶剂黄146 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 以70%的产率得到
    参考文献:
    名称:
    微波辅助合成二烷基次膦酸及稀土金属萃取中的结构反应性研究†
    摘要:
    二烷基次膦酸是通过微波辅助法合成的,具有高收率和广泛的底物适用性。一项结构反应研究表明,β位的位阻增加会导致提取率降低和稀土元素重分离活性降低。还进行了计算研究以了解空间效应。
    DOI:
    10.1039/c5ra23483b
  • 作为产物:
    参考文献:
    名称:
    GINER, JOSE-LUIS;MARGOT, CHRISTIAN;DJERASSI, CARL, J. ORG. CHEM., 54,(1989) N, C. 2117-2125
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • DEGRADATION OF POLYCYCLIC AROMATIC HYDROCARBONS TO RENDER THEM AVAILABLE FOR BIODEGRADATION
    申请人:Hong P.K. Andy
    公开号:US20080242875A1
    公开(公告)日:2008-10-02
    A method for the degradation of polycyclic aromatic compounds is disclosed that involves dissolving ozone in a bipolar solvent comprising a non-polar solvent in which is of sufficiently non-polar character to solubilized the polycyclic aromatic compounds, and a polar-water-compatible solvent which is fully miscible with the non-polar solvent to form a single phase with the non-polar solvent. The bipolar solvent with dissolved ozone is contacted with the polycyclic aromatic compounds to solubilize the polycyclic aromatic compounds and react the dissolved polycyclic aromatic compounds with the ozone to degrade the dissolved polycyclic aromatic compounds to oxygenated intermediates. The bipolar solvent is then mixed with sufficient water to form separate non-polar and polar phases, the non-polar phase comprising the non-polar solvent and the polar phase comprising the non-polar solvent and the oxygenated intermediates. The polar phase is then diluted and incubated with bacteria to biodegrade the oxygenated intermediates.
    揭示了一种降解多环芳烃化合物的方法,涉及将臭氧溶解在一种双极溶剂中,该溶剂包括一种非极性溶剂,其具有足够的非极性特性以溶解多环芳烃化合物,以及一种极性-水相容溶剂,与非极性溶剂完全互溶以形成与非极性溶剂相同的单一相。将含有溶解臭氧的双极溶剂与多环芳烃化合物接触,以溶解多环芳烃化合物并使溶解的多环芳烃化合物与臭氧反应,将溶解的多环芳烃化合物降解为含氧中间体。然后将双极溶剂与足够的水混合以形成分离的非极性和极性相,其中非极性相包括非极性溶剂,极性相包括非极性溶剂和含氧中间体。然后将极性相稀释并与细菌孵育以生物降解含氧中间体。
  • Scope and regiochemical control of the allylpotassium reaction in the synthesis of sterols with unsaturated side chains
    作者:Jose Luis Giner、Christian Margot、Carl Djerassi
    DOI:10.1021/jo00270a021
    日期:1989.4
  • Direct one-pot synthesis of terminal olefins and deuterio olefins from carboxylic acid chlorides
    作者:Jose Barluenga、Miguel Yus、Jose M. Concellon、Pablo Bernad
    DOI:10.1021/jo00166a041
    日期:1983.9
  • Selective dimerization of monosubstituted .alpha.-olefins by tantalacyclopentane catalysts
    作者:S. J. McLain、J. Sancho、R. R. Schrock
    DOI:10.1021/ja00537a035
    日期:1980.8
  • Microwave-assisted synthesis of dialkylphosphinic acids and a structure–reactivity study in rare earth metal extraction
    作者:Ruo-Bing Du、Huaying An、Suhui Zhang、Donghai Yu、Ji-Chang Xiao
    DOI:10.1039/c5ra23483b
    日期:——
    Dialkylphosphinic acids were synthesised by a microwave-assisted method with high yields and wide substrate applicability. A structure–reactivity study indicates that an increase in steric hindrance in the β position led to a decrease of extraction ratio and heavy rare earth element separation activity. A computational study was also conducted to understand the steric effect.
    二烷基次膦酸是通过微波辅助法合成的,具有高收率和广泛的底物适用性。一项结构反应研究表明,β位的位阻增加会导致提取率降低和稀土元素重分离活性降低。还进行了计算研究以了解空间效应。
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