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3,5-bis(2-propyl)-1,2,4-trioxolane | 1696-25-9

中文名称
——
中文别名
——
英文名称
3,5-bis(2-propyl)-1,2,4-trioxolane
英文别名
3,5-diisopropyl-[1,2,4]trioxolane;trans-2,5-Dimethylhexen-3-ozonid;1,2-Di-isopropyl-ethylen-ozonid;1,2-Diisopropyl-ethylenozonid;2,5-Dimethyl-hex-3-en-ozonid;Diisopropylozonid;3,5-Bis(1-methylethyl)-1,2,4-trioxolane;3,5-di(propan-2-yl)-1,2,4-trioxolane
3,5-bis(2-propyl)-1,2,4-trioxolane化学式
CAS
1696-25-9
化学式
C8H16O3
mdl
——
分子量
160.213
InChiKey
JOJUVLCDXZMONE-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:
    168.0±29.0 °C(Predicted)
  • 密度:
    0.964±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.7
  • 重原子数:
    11
  • 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:
    27.7
  • 氢给体数:
    0
  • 氢受体数:
    3

SDS

SDS:378fe0929b50a08d20754bde81b4ddea
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反应信息

  • 作为产物:
    描述:
    参考文献:
    名称:
    Formation of secondary ozonides in the gas phase low-temperature ozonation of primary and secondary alkenes
    摘要:
    在-40至20摄氏度下,一系列烯烃(RCHCH2,其中R=Et, Hex),反式-RHCCHR(R=Me, Et, Pri)以及Me2CCMe2的气相臭氧化反应,以及在-120至0摄氏度下乙烯H2CCH2的臭氧化反应,在氮气中体积分数为10-4的条件下、常压下进行了研究。通过GC-FTIR和GC-MS技术进行的补充产物分析,我们提供了确凿证据,表明在除Me2CCMe2外的所有情况下,次级烯烃臭氧化物都是高产率的主要产物。研究表明,反式-RHCCHR(R=Me, Et, Pri)在气相中转化为反式次级臭氧化物的立体选择性,与先前在溶液中观察到的相似,并且从RHCCH2(而非RHCCHR)生成的次级臭氧化物的产率随着温度的升高显著下降。
    DOI:
    10.1039/a807208f
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文献信息

  • Formation of secondary ozonides in the gas phase low-temperature ozonation of primary and secondary alkenes
    作者:Radek Fajgar、Josef Vítek、Yehuda Haas、Josef Pola
    DOI:10.1039/a807208f
    日期:——
    The gas-phase ozonation of a series of alkenes RCHCH2 (R = Et, Hex), trans-RHCCHR (R = Me, Et, Pri) and Me2CCMe2 at –40 to 20 °C, and that of ethene H2CCH2 at –120 to 0 °C at 10–4 v/v concentrations in N2 at atmospheric pressure have been studied. Using complementary product analysis by means of GC–FTIR and GC–MS techniques, we present conclusive evidence for the formation of secondary alkene ozonides as high-yield products in all instances except Me2CCMe2. It is shown that the stereoselectivity for the conversion of trans-RHCCHR (R = Me, Et, Pri) to trans-secondary ozonides in the gas phase is similar to that observed earlier in solution, and that the yields of secondary ozonides from RHCCH2, but not those from RHCCHR, significantly decrease with increasing temperature.
    在-40至20摄氏度下,一系列烯烃(RCHCH2,其中R=Et, Hex),反式-RHCCHR(R=Me, Et, Pri)以及Me2CCMe2的气相臭氧化反应,以及在-120至0摄氏度下乙烯H2CCH2的臭氧化反应,在氮气中体积分数为10-4的条件下、常压下进行了研究。通过GC-FTIR和GC-MS技术进行的补充产物分析,我们提供了确凿证据,表明在除Me2CCMe2外的所有情况下,次级烯烃臭氧化物都是高产率的主要产物。研究表明,反式-RHCCHR(R=Me, Et, Pri)在气相中转化为反式次级臭氧化物的立体选择性,与先前在溶液中观察到的相似,并且从RHCCH2(而非RHCCHR)生成的次级臭氧化物的产率随着温度的升高显著下降。
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同类化合物

青蒿氧烷 甲基3-甲基-1,2,4-三氧杂环戊烷-3-羧酸酯 烯丙基苯臭氧化物 5-乙酰基-3,5-二甲基-1,2,4-三氧杂环戊烷-3-甲腈 3-苯基-1,2,4-三氧杂螺[5.4]癸烷 3-甲基-3-苯基-1,2,4-三氧杂螺[5.4]癸烷 3,5-二苯基-1,2,4-三氧杂环戊烷 3,3-二丁基-1,2,4-三氧杂螺[5.4]癸烷 1-异丙基-4-甲基-2,3,7-三氧杂双环[2.2.1]庚烷 1-(5-甲氧基-3-甲基-1,2,4-三四氢呋喃-3-基)乙酮 1-(5,5-二甲基-1,2,4-三四氢呋喃-3-基)乙酮 1-(3,5,5-三甲基-1,2,4-三四氢呋喃-3-基)乙酮 1,2,4-三噁戊环,3-(1-氯乙烯基)- cis-1,4-Dimethyl-2,3,17-trioxabicyclo<12.2.1>heptadecane trans-1,4-Dimethyl-2,3,17-trioxabicyclo<12.2.1>heptadecane adamantane-2-spiro-3'-8'-hydroxy-8'-methyl-1',2',4'-trioxaspiro[4.5]decane adamantane-2-spiro-3'-8'-hydroxy-1',2',4'-trioxaspiro[4.5]decane (3-methyl-1,2,4-trioxolan-3-yl)hexanal (3-methyl-5-phenyl-5-trifluoromethyl-1,2,4-trioxolan-3-yl)pentanal trioxolane 7 3-tert-butyl-3-methyl-5-phenyl-5-trifluoromethyl-1,2,4-trioxolane 3-Cyano-5-cyclohexyl-3-isobutyl-1,2,4-trioxolane 5'-Cyano-5'-isobutylspiro (trans-5-cyano-5-phenyl-1,2,4-trioxolan-3-yl)-3-cyclopentanecarbaldehyde 5'-Cyano-5'-phenylspiro 3-Cyano-3,5-diphenyl-1,2,4-trioxolane 3-Cyano-3-phenyl-5-tert-butyl-1,2,4-trioxolane 3-tert-Butyl-3-methyl-1,2,4-trioxaspiro[5.4]decane (trans-5-cyano-3,5-dimethyl-1,2,4-trioxolan-3-yl)hexanal (trans-5-cyano-5-methyl-1,2,4-trioxolan-3-yl)hexanal 3,5-dimethyl-5-(3-oxopropyl)-1,2,4-trioxolane-3-carbonitrile (trans-5-cyano-5-methyl-1,2,4-trioxolan-3-yl)pentanal 3-Cyano-3-methyl-5-phenyl-1,2,4-trioxolane 3-Cyano-5-cyclohexyl-3-methyl-1,2,4-trioxolane (E)-3-methyl-5-[7-oxohept-5-enyl]-1,2,4-trioxolane-3-carbonitrile (Z)-3-methyl-5-[5-oxopent-1-enyl]-1,2,4-trioxolane-3-carbonitrile (E)-3-methyl-5-[6-oxohex-4-enyl]-1,2,4-trioxolane-3-carbonitrile 3-methyl-5-[(E)-5-oxopent-3-enyl]-1,2,4-trioxolane-3-carbonitrile (Z)-3-methyl-5-[4-methyl-7-oxohept-3-enyl]-1,2,4-trioxolane-3-carbonitrile 3-(Chloromethyl)-3-methoxy-1,2,4-trioxolane cis-3,5-bis-(chloromethyl)-3,5-dimethoxy-1,2,4-trioxolane trans-3,5-bis-(chloromethyl)-3,5-dimethoxy-1,2,4-trioxolane cis-adamantane-2-spiro-3'-8'-[[(4'-formyl-1'-piperazinyl)carbonyl]methyl]-1',2',4'-trioxaspiro[4.5]decane adamantane-2-spiro-3’-8’-hydroxymethyl-1’,2’,4’-trioxaspiro[4,5]decane 3-(Chloromethyl)-3-fluoro-1,2,4-trioxolane trans-3,5-Bis(chloromethyl)-3-fluoro-1,2,4-trioxolane methyl spiro3,7>decane-2,3'-<1,2,4>trioxolane>-5'-carboxylate 3-Cyano-3-phenyl-1,2,4-trioxolane 3-ethyl-1,24-trioxolane dispiro[adamantane-2,2'-[1,3,5]trioxolane-4',1''-cyclohexane]-3''-ol