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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 | 14384-47-5

中文名称
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
中文别名
——
英文名称
2,3-Dihydro-2,2,3,3,5,6-hexamethylpyrazine-1,4-dioxide
英文别名
2,2,3,3,5,6-Hexamethyl-2,3-dihydropyrazin-1,4-dioxid;2,2,3,3,5,6-hexamethyl-2,3-dihydro-pyrazine 1,4-dioxide;2,2,3,3,5,6-Hexamethyl-2,3-dihydro-pyrazin-1,4-dioxid;2,3-Dihydrohexamethylpyrazin-1,4-dioxid;2,2,3,3,5,6-Hexamethyl-4-oxidopyrazin-1-ium 1-oxide
2,2,3,3,5,6-六甲基-1-羰基-2,3-二氢吡嗪-1-正离子-4(1H)-醇酸化学式
CAS
14384-47-5
化学式
C10H18N2O2
mdl
——
分子量
198.265
InChiKey
DTHCHTIMNLLDQM-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:
    1.0
  • 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

SDS

SDS:4a5cbda978d20246118d1cc999805743
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反应信息

  • 作为反应物:
    参考文献:
    名称:
    Gagnon Janet L., Walters Thomas R., Zajac Walter W. (Jr), Buzby John H., J. Org. Chem, 58 (1993) N 24, S 6712-6715
    摘要:
    DOI:
  • 作为产物:
    描述:
    N,N’-二羟基-2,3-二甲基-2,3-丁二胺2,3-丁二酮乙醇 为溶剂, 反应 15.0h, 以63%的产率得到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
    参考文献:
    名称:
    关于单环α-二硝酮的反应性
    摘要:
    合成了一些单环α-二硝酮,并研究了它们与异氰酸酯反应时的反应性。
    DOI:
    10.1002/ardp.19803130210
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文献信息

  • Nitrones. Part VII. The photochemistry and cycloaddition of a monocyclic α-dinitrone
    作者:M. Lamchen、T. W. Mittag
    DOI:10.1039/j39680001917
    日期:——
    The photochemical isomerisation of the α-dinitrone, hexamethyl-2,3-dihydropyrazine 1,4-dioxide into a nitrone-oxaziridine 2,2,3,3,5,6-hexamethyl-1,4-diaza-7-oxabicyclo[4,1,0]hept-4-ene 4-oxide and a mixture of dioxaziridines is described. Cycloaddition of the nitrone-oxaziridine with acrylonitrile, and the structure of the adducts, are discussed. The i.r. spectra are used in the structural assignments
    α-地龙酮,1,4-二甲基六甲基-2,3-二氢吡嗪的光化学异构化为硝酮-恶唑烷2,2,3,3,5,6-六甲基-1,4-二氮杂-7-恶双环[描述了4,1,0]庚-4-烯4-氧化物和二恶唑烷的混合物。讨论了氮杂-恶唑烷与丙烯腈的环加成反应以及加合物的结构。红外光谱用于结构分配。该环加成反应表明原始的单环α-地尼酮对环加成反应的惰性不是由于吡嗪环,而是更可能是由于硝酮官能团的结合。
  • Interesting products derived from the reactions of 2,3-diamino-2,3-dimethylbutane
    作者:Janet L. Gagnon、Thomas R. Walters、Walter W. Zajac、John H. Buzby
    DOI:10.1021/jo00076a034
    日期:1993.11
    The diimine, N,N'-dibenzylidene-2,3-diamino-2,3-dimethylbutane (10), was successfully synthesized from 2,3-diamino-2,3-dimethylbutane (3) by reaction with excess benzaldehyde. The reaction of diimine 10 with permanganate/PTC at pH = 4.1 did not give the corresponding dinitrone 11 but unexpectedly gave 3-benzoyl-4,4,5,5-tetramethyl-2-phenylimidazoline (13) in 45% yield. The imidazoline 13 was independently prepared by benzoylation of 4,4,5,5-tetramethyl-2-phenylimidazoline (9) which had been synthesized from diamine 3 and methyl benzimidate. The cyclic alpha-dinitrone, 2,3-dihydro-2,2,3,3,5,6-hexamethylpyrazine 1,4-dioxide (4), synthesized from N,N'-dihydroxy-2,3-diamino-2,3-dimethylbutane (2) and 2,3-butanedione, underwent ozonolysis to yield the corresponding vicinal dinitro compound, 2,3-dimethyl-2,3-dinitrobutane (1), quantitatively.
  • Zur Reaktivität monocyclischer α-Dinitrone
    作者:Jürgen Schmidt、Gerwalt Zinner
    DOI:10.1002/ardp.19803130210
    日期:——
    Einige monocyclische α‐Dinitrone werden synthetisiert und ihre Reaktivität bei der Umsetzung mit Isocyanaten untersucht.
    合成了一些单环α-二硝酮,并研究了它们与异氰酸酯反应时的反应性。
  • Gagnon Janet L., Walters Thomas R., Zajac Walter W. (Jr), Buzby John H., J. Org. Chem, 58 (1993) N 24, S 6712-6715
    作者:Gagnon Janet L., Walters Thomas R., Zajac Walter W. (Jr), Buzby John H.
    DOI:——
    日期:——
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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