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Propylenozonid | 38787-96-1

中文名称
——
中文别名
——
英文名称
Propylenozonid
英文别名
propene ozonide;3-Methyl-1,2,4-trioxolane
Propylenozonid化学式
CAS
38787-96-1
化学式
C3H6O3
mdl
——
分子量
90.0788
InChiKey
IZHVFAKMAKGJLM-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:
    107.25°C (rough estimate)
  • 密度:
    1.1385 (rough estimate)

计算性质

  • 辛醇/水分配系数(LogP):
    0.4
  • 重原子数:
    6
  • 可旋转键数:
    0
  • 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

安全信息

  • 海关编码:
    2914190090

SDS

SDS:ebfea32fe5dbf585a34277b9f6213491
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反应信息

  • 作为产物:
    描述:
    三聚丙烯二氯甲烷臭氧 作用下, 生成 Propylenozonid
    参考文献:
    名称:
    乙烯,丙烯和异丁烯的臭氧层的气相红外光谱
    摘要:
    DOI:
    10.1021/j150540a030
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文献信息

  • The mechanism of ozone-alkene reactions in the gas phase. A mass spectrometric study of the reactions of eight linear and branched-chain alkenes
    作者:Richard I. Martinez、John T. Herron、Robert E. Huie
    DOI:10.1021/ja00403a031
    日期:1981.7
    The stable products of the low-pressure (4-8 torr (1 torr = 133.33 Pa)) gas-phase reactions of ozone with ethene, propene, 2-methylpropene, cis-2-butene, trans-2-butene, trans-2-pentene, 2,3-dimethyl-2-butene, and 2-ethyl- 1 -butene have been identified by using a photoionization mass spectrometer coupled to a stirred-flow reactor. The products observed are characteristic of (i) a primary Criegee split
    臭氧与乙烯、丙烯、2-甲基丙烯、顺-2-丁烯、反-2-丁烯、反- 2-戊烯、2,3-二甲基-2-丁烯和2-乙基-1-丁烯已通过使用耦合到搅拌流反应器的光电离质谱仪进行鉴定。观察到的产物具有以下特征:(i)初级 Criegee 分裂成氧代烷烃(醛或酮)和 Criegee 中间体,(ii)反应
  • Mechanism of the ozonolysis of ethylene-acetaldehyde mixtures
    作者:Jong In Choe、M. Kimberly Painter、Robert L. Kuczkowski
    DOI:10.1021/ja00322a025
    日期:1984.5
    On utilise de l'ethylene-D 2 -1,1 en presence d'acetaldehyde. Les rendements en ozonide d'ethylene-D 0 , -D 2 et D 4 et en ozonide de propylene-D 0 et -D 2 sont determines par RMN protonique, spectrometrie microonde et des mesures manometriques. On emploie un modele cinetique pour decrire le mecanisme de la reaction et pour estimer les rapports en produits finaux
    在使用 de l'ethylene-D 2 -1,1 en d'乙醛。Les rendements en ozonide d'ethylene-D 0 , -D 2 et D 4 et en ozonide de 丙烯-D 0 et -D 2 子确定标准RMN质子,光谱微量和des mesures manometriques。On emploie un modele cinetique pour decrire le mecanisme de la reaction et pour estimer les rapports en produits finaux
  • Formation of secondary ozonides in the gas-phase ozonolysis of simple alkenes
    作者:Peter Neeb、Osamu Horie、Geert K Moortgat
    DOI:10.1016/s0040-4039(97)82946-2
    日期:1996.12
    formed in the gas-phase ozonolysis of ethene with added acetaldehyde and acetone, respectively. Combined with the formation of hydroperoxymethyl formate and methoxymethyl hydroperoxide in the ethene-ozone reaction system in the presence of HCOOH and CH3OH, respectively, formation of the secondary ozonides reveals a close similarity between the gas-phase and the liquid-phase ozonolysis of alkenes.
    在分别加入乙醛和丙酮的乙烯气相臭氧分解反应中,形成了次级丙烯臭氧化物和异丁烯臭氧化物。分别在HCOOH和CH 3 OH存在下在乙烯-臭氧反应系统中形成过氧化氢甲酸甲酸酯和过氧化甲氧基甲基氢过氧化物,形成第二种臭氧层表明在气相和液相臭氧分解过程中烯烃。
  • Ozonolysis of enol ethers: formation of 3-alkoxy-1,2-dioxolanes by concerted addition of a carbonyl oxide to an enol ether
    作者:Helmut Keul、Robert L. Kuczkowski、Hyung-Soo Choi
    DOI:10.1021/jo00218a024
    日期:1985.9
  • Mechanism of the ozonolysis of propene in the liquid phase
    作者:Jong In Choe、M. Srinivasan、R. L. Kuczkowski
    DOI:10.1021/ja00352a030
    日期:1983.7
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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