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2,3-Dimethyl-4a,5,6,7,8,8a-hexahydro-quinoxaline 1,4-dioxide | 152860-47-4

中文名称
——
中文别名
——
英文名称
2,3-Dimethyl-4a,5,6,7,8,8a-hexahydro-quinoxaline 1,4-dioxide
英文别名
2,3-Dimethyl-4-oxido-4a,5,6,7,8,8a-hexahydroquinoxalin-1-ium 1-oxide
2,3-Dimethyl-4a,5,6,7,8,8a-hexahydro-quinoxaline 1,4-dioxide化学式
CAS
152860-47-4
化学式
C10H16N2O2
mdl
——
分子量
196.249
InChiKey
GVQITOMIIWGZEP-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

计算性质

  • 辛醇/水分配系数(LogP):
    0.4
  • 重原子数:
    14
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.8
  • 拓扑面积:
    46.4
  • 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:
    Derivatives of Dihydropyrazine-1,4-Dioxide, 3-Imidazoline 3-Oxide, and α-Phenyl Nitrones with Functional Groups as New Spin Traps in Solution and in the Gas Phase
    摘要:
    The title compounds, acyclic phenyl nitrones with functional groups, cyclic dinitrones with conjugated or isolated double bonds, and imidazoline nitrones are studied as spin traps (ST) for short-lived free radicals (R) generated photochemically in solution and in the gas phase. New STs are efficient in trapping OH, hydroxyalkyl, or HO2 radicals. EPR spectra of the spin adducts (SA) of studied dinitrones are triplets of doublets characteristic of the nitroxides with one radical center. Imidazoline ST with amino nitrogen exhibits pH-dependent hyperfine splittings of its SAs. Some spin traps were shown to be efficient in detecting R in the atmospheric experiments.
    DOI:
    10.1021/jp960438e
  • 作为产物:
    描述:
    2,3-丁二酮 、 N,N'-dihydroxycyclohexane-1,2-diamine 以 乙醇 为溶剂, 反应 3.0h, 以96%的产率得到2,3-Dimethyl-4a,5,6,7,8,8a-hexahydro-quinoxaline 1,4-dioxide
    参考文献:
    名称:
    Interaction of 1,2-bishyroxylamines with 1,2-dicarbonyl compounds. Isolation and properties of 2,3-dihydropyrazine-1,4-dioxides
    摘要:
    DOI:
    10.1007/bf00529884
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文献信息

  • Derivatives of Dihydropyrazine-1,4-Dioxide, 3-Imidazoline 3-Oxide, and α-Phenyl Nitrones with Functional Groups as New Spin Traps in Solution and in the Gas Phase
    作者:Galina G. Dultseva、Galina I. Skubnevskaya、Aleksei Ya. Tikhonov、Dmitrii G. Mazhukin、Leonid B. Volodarsky
    DOI:10.1021/jp960438e
    日期:1996.1.1
    The title compounds, acyclic phenyl nitrones with functional groups, cyclic dinitrones with conjugated or isolated double bonds, and imidazoline nitrones are studied as spin traps (ST) for short-lived free radicals (R) generated photochemically in solution and in the gas phase. New STs are efficient in trapping OH, hydroxyalkyl, or HO2 radicals. EPR spectra of the spin adducts (SA) of studied dinitrones are triplets of doublets characteristic of the nitroxides with one radical center. Imidazoline ST with amino nitrogen exhibits pH-dependent hyperfine splittings of its SAs. Some spin traps were shown to be efficient in detecting R in the atmospheric experiments.
  • Interaction of 1,2-bishyroxylamines with 1,2-dicarbonyl compounds. Isolation and properties of 2,3-dihydropyrazine-1,4-dioxides
    作者:D. G. Mazhukin、A. Ya. Tikhonov、L. B. Volodarskii、E. P. Konovalova
    DOI:10.1007/bf00529884
    日期:1993.4
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同类化合物

N,N-二氧化吡嗪 5-异丙基-2,3-二甲基吡嗪1,4-二氧化物 3-甲基-4-氧代吡嗪-1-鎓1-氧化物 2-甲基-2-亚硝基丙腈 2,5-二甲基吡嗪 1,4-二氧化物 2,3-二氢-3,3-二甲基-吡嗪醇 1,4-二氧化物 2,3,3,5,6-五甲基-1-氧代-2,3-二氢吡嗪-1-鎓-4(1H)-醇 2,2,3,3,5,6-六甲基-1-羰基-2,3-二氢吡嗪-1-正离子-4(1H)-醇酸 1,2-二[1-(1,1-二甲基乙基)-2,2-二甲基丙基]二氮烯1,2-二氧化物 (5-甲基-1,4-二氧代-2-吡嗪基)甲醇 trans-Nitrosomethan-dimer 1,2-Bis(2,2-diethoxyethyl)-2-oxodiazan-2-ium-1-olate nitrosocyclohexane dimer Dimeres-2-Chlor-1-nitroso-cyclopentan 2,5-Dichlor-3,6-diethylpyrazin-1,4-dioxid [Oxido(propan-2-yl)amino]-oxo-propan-2-ylazanium Tetrachlorpyrazin-bis-N-oxid Bis-(5-methyl-hexa-3,4-dienyl)-diazene N,N'-dioxide 2,3,4,6,7,8,9,10-Octahydro-1H-cyclohepta[b]quinoxaline 5,11-dioxide 2,7-Dicyano-2,7-dimethyl-3,6-diazaocta-3,5-dien-3,6-dioxide 2,3-Dimethyl-4a,5,6,7,8,8a-hexahydro-quinoxaline 1,4-dioxide 3-(2-Methoxyethoxy)-4-oxidopyrazin-1-ium 1-oxide 2-propylpyrazine 1,4-dioxide 2-methyl-5,6,7,8-tetrahydroquinoxaline 1,4-dioxide 1-nitrosodecane dimer 2,2,3,3-Tetramethyl-2,3-dihydropyrazin-1,4-dioxid 2,6-dimethylpyrazine-N,N'-dioxide 2,3-dimethylpyrazine 1,4-dioxide 2,5-Dichlor-3,6-dimethylpyrazin-1,4-dioxid 2,5-di-iso-propylpyrazine 1,4-dioxide 2,3,5-trimethylpyrazine-N,N'-dioxide 2-methoxymethyl-5-methylpyrazine-1,4-dioxide 3-hydroxy-2,2-dimethyl-2,3,5,6,7,8-hexahydroquinoxaline 1,4-dioxide 1,2-Bis(2-chloro-2-methylpentan-3-yl)-2-oxodiazan-2-ium-1-olate Cyclohexyl(ethenyl)oxoammonium 1-Oxo-1,2-diazet-1-ium-2(1H)-olate 2,3-(bisbromomethyl)-4a,5,6,7,8,8a-hexahydroquinoxaline-1,4-dioxide Di-tert-butyl-nitroxid 5,6-bis(bromomethyl)-2,2-dimethyl-3-methoxy-2,3-dihydropyrazine 1,4-dioxide 2,2,5,6-tetramethyl-3-methoxy-2,3-dihydropyrazine 1,4-dioxide 3-hydroxy-2,2,5,6-tetramethyl-2,3-dihydropyrazine 1,4-dioxide 2,5-dichloro-3,6-dipropylpyrazine 1,4-dioxide 2-Chlor-1-nitrosohexadecan-Dimer 2,5-dichloro-3,6-diisobutyl-pyrazine 1,4-dioxide 2-chloro-pyrazine 1,4-dioxide N,N'-Dimethyl-glyoxaldiimin-N,N'-dioxid N,N'-diheptyldiazene N,N'-dioxide 2-methyl-2-nitrosopropane dimer [(2S)-2-chlorohexadecyl]-[[(2R)-2-chlorohexadecyl]-oxidoamino]-oxoazanium [(2R)-2-chlorohexadecyl]-[[(2R)-2-chlorohexadecyl]-oxidoamino]-oxoazanium