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1,4-dimethyl-2,3,7-trioxa-bicyclo[2.2.1]hept-5-ene | 45722-89-2

中文名称
——
中文别名
——
英文名称
1,4-dimethyl-2,3,7-trioxa-bicyclo[2.2.1]hept-5-ene
英文别名
1,4-Dimethyl-2,3,7-trioxabicyclo[2.2.1]hept-5-ene
1,4-dimethyl-2,3,7-trioxa-bicyclo[2.2.1]hept-5-ene化学式
CAS
45722-89-2
化学式
C6H8O3
mdl
——
分子量
128.128
InChiKey
HDRUBHQNIALXHQ-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:
    112.8±40.0 °C(Predicted)
  • 密度:
    1.266±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.6
  • 重原子数:
    9
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    27.7
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Dihydrogen Trioxide (HOOOH) Photoelimination from a Platinum(IV) Hydroperoxo-Hydroxo Complex
    摘要:
    Photolysis (380 nm) of trans-Pt(PEt3)(2)(Cl)(OH)(OOH)(4-trifluoromethylphenyl) (1) at -78 degrees C in acetone-d(6) or toluene-d(8) yields HOOOH (16-20%) and trans-Pt(PEt3)(2)(Cl)(4-trifluoromethylphenyl) (2). Also observed in acetone-d(6) are H2O2, (CD3)(2)C(OH)(OOH), and (CD3)(2)C(OOH)(2). Thermal decomposition or room-temperature photolysis of 1 gives O-2, water, and 2. Computational modeling (DFT) suggests two intramolecular hydrogen-bonding-dependent triplet pathways for the photolysis and two possible pathways for the thermolysis, one involving proton transfer from the OOH to the OH ligand and the other homolysis of the PtOOH bond, abstraction of the OH ligand, and decomposition of the resulting H2O3. Trapping studies suggest the latter pathway.
    DOI:
    10.1021/ja507263f
  • 作为产物:
    描述:
    参考文献:
    名称:
    将单线态氧添加到共轭二烯中。内过氧化物形成机制
    摘要:
    Etude cinetique des reactors de l'oxygene singulet avec divers furanes substitues-2 et dissubstitues symetriquement-2,5
    DOI:
    10.1021/ja00356a046
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文献信息

  • Mechanism of endoperoxide formation. 3. Utilization of the Young and Carlsson kinetic techniques
    作者:Edward L. Clennan、M. E. Mehrsheikh-Mohammadi
    DOI:10.1021/ja00335a040
    日期:1984.11
    Determination des constantes de vitesse d'additions de l'oxygene singulet a trente-neuf furannes et cyclopentadienes
    Determination des constantes de vitesse d'additions de l'oxygene singulet a trente-neuf furannes et cyclopentadienes
  • Anomalous ozonolysis products in the addition of singlet oxygen to methoxymethylfurans
    作者:Ben L. Feringa、Robert J. Butselaar
    DOI:10.1016/s0040-4039(01)90346-6
    日期:1981.1
    The rearrangement of cyclobutadiene ozonides, related to “anomalous ozonolysis”, has been elucidated.
    已经阐明了与“异常臭氧分解”有关的环丁二烯臭氧化物的重排。
  • A crown ozonide and its rearrangement to a macrocyclic lactone
    作者:Ben L. Feringa
    DOI:10.1016/s0040-4039(01)90345-4
    日期:1981.1
    The addition of singlet oxygen to 2,5-furo-18-crown-6 yields a crown ozonide, which rearranges quantitatively to a macrocyclic lactone.
    将单线态氧添加到2,5-furo-18-crown-6中可产生冠状臭氧化物,其定量重排为大环内酯。
  • Cyclic peroxides. 92. Oxygen atom transfer by furan endoperoxides
    作者:Waldemar Adam、Augusto Rodriguez
    DOI:10.1021/ja00521a082
    日期:1980.1
  • Photooxygenation of furans in the presence of trimethylsilyl cyanide. Oxidative cyanation of furans
    作者:Isao Saito、Yueh-Hsiung Kuo、Teruo Matsuura
    DOI:10.1016/s0040-4039(00)84636-5
    日期:——
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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-1,2,5-三氧杂螺[5.5]十一烷 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-异丙基环戊烯-1臭氧 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-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-(3-氯-3-乙基-2-甲基噁丙环基)-3-甲基- 1,2,4-三噁戊环,3-(1-氯乙烯基)- (3R,5R)-3-异丙基-5-丙基-1,2,4-三氧杂环戊烷 1,3-Dioxoldioxetan (3R,5R)-3,5-dimethyl-1,2,4-trioxolane (4aR,7aR,11aS,11bS)-6-Ethoxy-hexahydro-1,3,5,7,9,11-hexaoxa-6-phospha-dibenzo[a,c]cycloheptene O2,O4;O3,O5-dimethanediyl-1,6-dideoxy-D-glucitol 2α-Phenyl-bicyclo<3.3.1>nonan-2β.3β-oxid 5,14,15-Trioxadispiro<3.1.7.2>pentadecan 1,4-ditert-butyl-2,3,7-trioxabicyclo[2.2.1]hept-5-ene meso-Tricyclo<7,4,0,02,7>-1-tridecenozonid 3-heptyl-5-methoxy-5-(trifluoromethyl)-1,2,4-trioxolane 2,2-diethyl-5-(2-vinyl-buta-1,3-dienyl)-[1,3]dioxolane-4-carbaldehyde 3,3-Dicyclopropyl-1,2,4-trioxolan 3-cyclohexyl-5-methoxy-5-(trifluoromethyl)-1,2,4-trioxolane 1,4,4-Trimethyl-2,3,5,6,11-pentaoxabicyclo[5.3.1]undecane 1-Methyl-4-pentyl-2,3,5,6,11-pentaoxabicyclo[5.3.1]undecane Propylenozonid-d(1) acrolein (R,R)-1,2-dicyclohexylethylene acetal 3-methoxy-1-tert-butyl-1,2,4,5-tetraoxaspiro[5.5]undecane trans-3.5-Bis-chlormethyl-1.2.4-trioxolan Ozonid des Aethylidenadamantans(5) 3-tert-Butyl-3-(2-tert-butyl-2-oxiranyl)-1,2,4-trioxolan Ozonid des Neopentylidenadamantans(6) cis-3-ethoxy-3-(trifluoromethyl)-5-phenyl-1,2,4-trioxolane (1R,2S,3R,4R,5R)-1,7-anhydro-1-(hydroxymethyl)-2,3,4-tri-O-(methoxymethyl)-5-methyl-1,2,3,4-cyclohexanetetraol 5,5'-diphenyl-3,3'-bi-1,2,4-trioxolane 5-heptyl-5'-phenyl-3,3'-bi-1,2,4-trioxolane Ozonid des Methyladamantans(4) cis-3,5-dimethyl-3,5-diethyl-1,2,4-trioxolane 2-[[3,5-diethyl-2,2-di(propan-2-yloxy)-1,4,2λ5-dioxaphospholan-2-yl]methyl]-3,5-diethyl-2,2-di(propan-2-yloxy)-1,4,2λ5-dioxaphospholane cis-3,5-dimethyl-3,5-diethyl-1,2,4-trioxolane trans-3-ethoxy-3-(trifluoromethyl)-5-phenyl-1,2,4-trioxolane