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1-甲基-1-丙基环己烷 | 4258-93-9

中文名称
1-甲基-1-丙基环己烷
中文别名
——
英文名称
1-Methyl-1-propyl-cyclohexan
英文别名
1-Methyl-1-propylcyclohexane
1-甲基-1-丙基环己烷化学式
CAS
4258-93-9
化学式
C10H20
mdl
——
分子量
140.269
InChiKey
SSOKTUYAEOXEPO-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:
    -84.33°C (estimate)
  • 沸点:
    174.35°C
  • 密度:
    0.8101

计算性质

  • 辛醇/水分配系数(LogP):
    5
  • 重原子数:
    10
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

安全信息

  • 海关编码:
    2902199090

SDS

SDS:7db7931d567598526162d3e3585ae573
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上下游信息

  • 上游原料
    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-甲基-1-丙基环己烷 、 alkaline earth salt of/the/ methylsulfuric acid 生成 正丙基苯甲苯
    参考文献:
    名称:
    Study in the Terpene Series. XXII.1a Synthesis, Physical Constants and Catalytic Dehydrogenation of 1-Methyl-1-ethyl-, 1-Methyl-1-n-propyl- and 1-Methyl-1-isopropylcyclohexane1b
    摘要:
    DOI:
    10.1021/ja01615a044
  • 作为产物:
    描述:
    参考文献:
    名称:
    Buck et al., Journal of the Institute of Petroleum, 1948, vol. 34, p. 350
    摘要:
    DOI:
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文献信息

  • High-performance ring-opening catalysts based on iridium-containing zeolite Beta in the hydroconversion of decalin
    作者:Dominic Santi、Tobias Holl、Vincenzo Calemma、Jens Weitkamp
    DOI:10.1016/j.apcata.2013.01.020
    日期:2013.3
    Decalin was converted in a flow-type reactor under a hydrogen pressure of 5.2 MPa on Ir/H,A-Beta zeolite catalysts, where A stands for an alkali metal cation. In one series of catalysts, the Ir content was 3 wt.%, and the nature of A was varied from lithium to cesium. In a second series, the iridium content in Ir/H,Cs-Beta was varied from 1 to 5 wt.%. On some of these catalysts, open-chain decanes (OCDs) were formed with unprecedented selectivities and yields of up to 47 and 44%, respectively. The term "High-Performance Ring-Opening Catalysts" (HIPEROCs) was defined. Evidence is presented for hydrogenolysis on the metal being the main ring-opening mechanism on HIPEROCs. The main function of the Bronsted-acid sites is a mild isomerization of six-membered into five-membered naphthenic rings which are much easier to open by hydrogenolysis. Valuable mechanistic information can be deduced from the carbon-number distributions and the naphthenes vs. alkanes content of the hydrocracked products (C-9-). (c) 2013 Elsevier B.V. All rights reserved.
  • Radshabli-Seidowa et al., Zhurnal Obshchei Khimii, 1959, vol. 29, p. 2212,2216, 2217; engl. Ausg. S. 2179, 2180
    作者:Radshabli-Seidowa et al.
    DOI:——
    日期:——
  • Bolestova, G. I.; Parnes, Z. N., Journal of Organic Chemistry USSR (English Translation), 1987, vol. 23, p. 32 - 36
    作者:Bolestova, G. I.、Parnes, Z. N.
    DOI:——
    日期:——
  • Chromow et al., Doklady Akademii Nauk SSSR, 1954, vol. 96, p. 295
    作者:Chromow et al.
    DOI:——
    日期:——
  • Bolestova, G. I.; Parnes, Z. N.; Kursanov, D. N., Journal of Organic Chemistry USSR (English Translation), 1983, p. 2175 - 2179
    作者:Bolestova, G. I.、Parnes, Z. N.、Kursanov, D. N.
    DOI:——
    日期:——
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