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6-(hydroxyiminomethyl)-4-methyl-1-phenylpyridazinium-3-sulfonate | 158468-22-5

中文名称
——
中文别名
——
英文名称
6-(hydroxyiminomethyl)-4-methyl-1-phenylpyridazinium-3-sulfonate
英文别名
6-[(E)-hydroxyiminomethyl]-4-methyl-1-phenylpyridazin-1-ium-3-sulfonate
6-(hydroxyiminomethyl)-4-methyl-1-phenylpyridazinium-3-sulfonate化学式
CAS
158468-22-5;168138-87-2
化学式
C12H11N3O4S
mdl
——
分子量
293.303
InChiKey
LPKWZSAGRALARV-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):
    1.6
  • 重原子数:
    20
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    115
  • 氢给体数:
    1
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    Synthese und Charakterisierung von Stilbazoliumfarbstoffen mit mesoionischer 1,2-Diaziniumstruktur
    摘要:
    Pyridazinium salts of typ 1 react with substituted aromatic and heteroaromatic aldehydes 2a, e-h, 8a-c and trans-p-dimethylamino-cinnamaldehyde 3a to the charge transfer dyes 4a-h, 5a-d, 9a-c. They absorb in the range between 380 and 660 degrees nm. The dehydratisation of the aldoxime group in 4, 5 to the nitril group under formation of 6, 7a-d causes a bathochromic shift of the absorption band up to 110 nm. The UV-VIS data are discussed dependent on the structure of the dyes.
    DOI:
    10.1002/prac.19953370175
  • 作为产物:
    参考文献:
    名称:
    A mesoionic pyridazinium sulfonate; an unexpected reaction product
    摘要:
    The title compound is an 'inner' salt: 6-(hydroxy-iminomethyl)-4-methyl-1-phenylpyridazinium-3-sulfonate, C12H11N3O4S (1). The pyridazinium ring is almost planar and twisted approximately 50-degrees out of the benzene ring plane. The oxime -OH group forms an intermolecular hydrogen bond to one of the sulfonate O atoms. The identification of (1) has revealed an unusual rearrangement.
    DOI:
    10.1107/s0108270193013022
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文献信息

  • Fanghaenel, E.; Hucke, A.; Hasan, H., Journal fur Praktische Chemie - Chemiker-Zeitung, 1995, vol. 337, # 2, p. 104 - 108
    作者:Fanghaenel, E.、Hucke, A.、Hasan, H.、Ullrich, K.、Radeglia, R.、Simonsen, O.
    DOI:——
    日期:——
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同类化合物

酸四嗪 甲四嗪-氨基叔丁酯 四嗪-活性脂 四嗪-氨基叔丁酯 嘧啶并[4,5-e]-1,2,3,4-四嗪 二甲基-1,2,4,5-四嗪 二氯均四嗪 METHYLTETRAZINE-ACID,甲基四嗪-羧基 6-苯基-1,2,4,5-四嗪-3-胺 6-乙基-1,2,4,5-四嗪-3-胺 6-丁基氨基-3-(3,5-二甲基吡唑-1-基)四嗪 6-(3,5-二甲基吡唑-1-基)-1,2,4,5-四嗪-3-胺 3-苯基-6-(吡啶-2-基)-1,2,4,5-四嗪 3,6-二苯基-1,2,4,5-四嗪 3,6-二溴-1,2,4,5-四嗪 3,6-二氨基-1,2-二氢-1,2,4,5-四嗪盐酸盐 3,6-二-4-吡啶基-1,2,4,5-四嗪 3,6-二-2-吡啶基-1,2,4,5-四嗪 3,6-二(噻吩-2-基)-1,2,4,5-四嗪 3,6-二(3-吡啶基)-1,2,4,5-四氮杂苯 3,6-二(3,5-二甲基-1H-吡唑-1-基)-1,2,4,5-四嗪 1-[6-(3,5-二甲基吡唑-1-基)-1,2,4,5-四嗪-3-基]-2-(丙-2-亚基)肼 1,2-二氢-1,2,4,5-四嗪-3,6-二酮 1,2,5-噁二唑-3-胺,4-[(5-甲基-2H-四唑-2-基)甲基]- 1,2,4,5]四嗪-3,6-二羧酸 1,2,4,5-四嗪-3-胺 1,2,4,5-四嗪-3,6-二羧酸二甲酯 1,2,4,5-四嗪,3-甲氧基-6-苯基- 1,2,4,5-四嗪 (9CI)-吡咯并[2,1-d]-1,2,3,5-四嗪 (6-肼基-1,2,4,5-四嗪-3-基)肼 3,6-Dicyclopropyl-s-tetrazin 3-Methyl-4-methylaminotriazol-1-oxid 1,2,4,5-Tetrazin-3-amine, 6-cyclohexyl- 7-amino-2-trifluoromethyl-6-(5-trifluoromethyl-1,3,4-thiadiazol-2-yl)-4,4a,5,6-tetra-hydroimidazo[1,5-d][1,3,4]thiadiazin-6-ium pentaiodide 3,6-bis(ethylamino)-1,2,4,5-tetrazine Gtersunqcxeonk-uhfffaoysa- aminotetrazine argon 3-amino-s-tetrazine*Ar2 N-(2-chloro-1-methoxyethyl)-6-(3,5-dimethyl-1H-pyrazol-1-yl)-1,2,4,5-tetrazin-3-amine 3,6-di(2-cyclopentylidenehydrazino)-1,2,4,5-tetrazine 4,4'-(butane-2,3-diylidenebis(azaneylylidene))bis(4H-1,2,4-triazole-3-thiol) 6-Isopropyl-s-triazolo<4,3-b>-s-tetrazin-3-thiol 3-amino-6-(3,5-diamino-1,2,4-triazol-1-yl)-1,2,4,5-tetrazine 3,6-bis(4-bromo-3,5-dimethylpyrazol-1-yl)-1,2,4,5-tetrazine 1,4-s-Tetrazin-15N2 N-(sec-butyl)-6-(3,5-dimethyl-1H-pyrazol-1-yl)-1,2,4,5-tetrazin-3-amine 1,2-Di-4-pyridazinylethanone oxime trans-Pt(S[CN4(C2H5)])2(PMe3)2