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Di-tert-butyl-nitroxid | 44871-19-4

中文名称
——
中文别名
——
英文名称
Di-tert-butyl-nitroxid
英文别名
di-tert-Butyl nitroxyl;ditert-butyl(oxo)azanium
Di-tert-butyl-nitroxid化学式
CAS
44871-19-4
化学式
C8H18NO
mdl
——
分子量
144.237
InChiKey
ZYVDOMIPNQUMNV-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):
    1.3
  • 重原子数:
    10
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    20.1
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为产物:
    描述:
    二叔丁基硝基氧 在 hexachloroiridate(IV) 作用下, 生成 Di-tert-butyl-nitroxid
    参考文献:
    名称:
    涉及叠氮基的电子转移反应
    摘要:
    DOI:
    10.1021/j100407a042
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文献信息

  • Method for the functionalization of conjugated or conjugatable derivatives assisted by a tempo-type electrophoric mediator
    申请人:Belgsir El Mustapha
    公开号:US20070197790A1
    公开(公告)日:2007-08-23
    The invention relates to a method for the functionalization of a chemical molecule having at least two double bonds or containing a double bond which is conjugated with a structure that is rich in electrons in the presence of a TEMPO-type electrophoric mediator and a nucleophilic agent. The functionalization method can also include a system for electrochemical regeneration of the electrophoric mediator.
  • Alpha-Hydrogen Substituted Nitroxyls And Derivatives Thereof As Catalysts
    申请人:Technion Research and Development Foundation Ltd.
    公开号:US20140350258A1
    公开(公告)日:2014-11-27
    Novel alpha-hydrogen substituted nitroxyl compounds and their corresponding oxidized (oxoammonium cations) and reduced (hydroxylamine) forms, and the use of such compounds, inter alia, for oxidation of primary and secondary alcohols to aldehydes and ketones, respectively; resolution of racemic alcohols; desymmetrization of meso-alcohol; as radicals and spin trapping reagents; and as polymerization agents. Processes for preparing the novel nitroxyl/oxoammonium/hydroxylamine compounds from the corresponding amines, and certain novel amine derivatives and their uses. The compounds and amine precursors are useful as ligands for transition metals and as organocatalysts in e.g., aldol reactions.
  • US9475774B2
    申请人:——
    公开号:US9475774B2
    公开(公告)日:2016-10-25
  • Electron-transfer reactions involving the azidyl radical
    作者:M. S. Ram、David M. Stanbury
    DOI:10.1021/j100407a042
    日期:1986.7
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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