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1,10-ethyleneisoalloxazinium chloride | 114853-42-8

中文名称
——
中文别名
——
英文名称
1,10-ethyleneisoalloxazinium chloride
英文别名
1,10-ethanoisoalloxazinium chloride;1,10-ethyleneisoalloxazine chloride;4,6-Dioxo-2,4,5,6-tetrahydro-1H-benzo[g]imidazo[1,2,3-ij]pteridin-12-ium chloride;8,11,13-triaza-1-azoniatetracyclo[7.6.1.02,7.013,16]hexadeca-1(16),2,4,6,8-pentaene-10,12-dione;chloride
1,10-ethyleneisoalloxazinium chloride化学式
CAS
114853-42-8
化学式
C12H9N4O2*Cl
mdl
——
分子量
276.682
InChiKey
UKQDCOMWRMLNKZ-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):
    -3.46
  • 重原子数:
    19
  • 可旋转键数:
    0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    66.2
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    乙酸酐1,10-ethyleneisoalloxazinium chloride 作用下, 以 三氟乙酸 为溶剂, 反应 1.0h, 以54%的产率得到1,10-ethano-5-acetyl-1,5-dihydrolumiflavin
    参考文献:
    名称:
    N1,N10-Ethylene-bridged high-potential flavins: synthesis, characterization, and reactivity
    摘要:
    N-1,N-10-Ethyleneisoalloxazinium chloride and its 8-Cl-, 7-CF3-, and 3-CH3-7-CF3-substituted analogs were synthesized for the purpose of exhibiting thermal reactivity with organic substrates. The new flavins were characterized spectroscopically and electrochemically, and were found to react with amines, thiols, and phenylhydrazine, the latter case exhibiting catalytic aerobic recycling. Reactions of aliphatic benzylic and cyclopropyl amines with the 7-CF3 analog were also compared to their oxidations by tris(phenanthroline)iron(III). All reactions of the flavinium salts appear to occur through heterolytic rather than homolytic mechanisms. (C) 2001 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(01)00313-1
  • 作为产物:
    描述:
    N-(2-硝基苯基)乙醇胺氯化亚砜 、 palladium on activated charcoal 、 甲酸铵硼酸溶剂黄146 作用下, 以 甲醇 为溶剂, 反应 21.0h, 生成 1,10-ethyleneisoalloxazinium chloride
    参考文献:
    名称:
    用合成的黄素类似物体内调节辅因子平衡
    摘要:
    报道了一种使用合成黄素类似物调节全细胞生物转化体内辅因子平衡的新策略。观察到该系统的高效率,易于操作和良好的适用性。共聚焦激光扫描显微镜用于验证合成的黄素类似物可以直接渗透到大肠杆菌细胞中,而无需修饰细胞膜。这项工作提供了一种有前途的细胞内氧化还原调节方法,以构建更有效的细胞工厂。
    DOI:
    10.1002/anie.201810881
  • 作为试剂:
    描述:
    烯丙醇2,2,6,6-四甲基哌啶氧化物硝基甲烷氧气1,10-ethyleneisoalloxazinium chloride 作用下, 反应 8.0h, 以94%的产率得到丙烯醛
    参考文献:
    名称:
    黄素硝基烷氧化酶模拟了与NOx / TEMPO催化的相容性:醇,二醇和醚的需氧氧化。
    摘要:
    仿生黄素有机催化剂将硝基甲烷氧化为甲醛和NO x,为乙醇,二醇和醚的需氧TEMPO氧化提供了一种相对无毒,无苛刻且廉价的催化NO 2来源。醇被氧化成醛或酮,环醚被氧化成酯,末端二醇被氧化成内酯。NO x和甲醛的原位捕集表明氧化Nef过程使人联想到黄素蛋白硝基烷氧化酶的反应性,这是通过相对稳定的1,10-桥联黄素实现的。无金属的黄素/ NO x / TEMPO催化循环具有独特的相容性,尤其是与其他Nef和NO x相比生成过程,并显示出黄素催化亚砜形成的选择性。脂肪族醚通过这种方法被氧化,如(-)-氨氧化物转化为(+)-香紫苏内酯所证明的。
    DOI:
    10.1021/acs.joc.0c01013
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文献信息

  • CHEMICAL REGENERATION METHOD OF OXIDIZED COENZYME NAD (P)+
    申请人:NANJING TECH UNIVERSITY (CN)
    公开号:US20170114085A1
    公开(公告)日:2017-04-27
    It discloses a chemical regeneration method of oxidized coenzyme NAD(P) + which is under an oxygen or air atmosphere condition, adding a catalytic amount of bridged flavin, and oxidizing NAD(P)H to obtain NAD(P) + . The catalyst for regeneration of cofactor is cheap and easily available small organic molecule having no noble metal; this regeneration system can regenerate NADH and NADPH; this regeneration system has a wide pH range and temperature range, being applicable to various oxidation reactions catalyzed by nicotinamide-dependent oxidoreductase.
    它揭示了一种化学再生方法,用于在氧气或空气氛围条件下氧化辅酶NAD(P)+,添加一个催化量的桥联黄素,并氧化NAD(P)H以获得NAD(P)+。辅酶再生的催化剂是一种廉价且易获得的小有机分子,不含贵金属;这种再生系统可以再生NADH和NADPH;这种再生系统具有较宽的pH范围和温度范围,适用于由烟酰胺依赖氧化还原酶催化的各种氧化反应。
  • Chemoselective sulfide oxidation mediated by bridged flavinium organocatalysts
    作者:Barrie J. Marsh、David R. Carbery
    DOI:10.1016/j.tetlet.2010.02.164
    日期:2010.4
    The chemoselective oxidation of sulfides to sulfoxides, catalysed by bridged, tetracyclic flavinium catalysts is presented. The flavinium catalysts are easily prepared via a telescoped three-step process. A range of sulfoxides is accessed in excellent yield and chemoselectivity. (C) 2010 Elsevier Ltd. All rights reserved.
  • Regulating Cofactor Balance In Vivo with a Synthetic Flavin Analogue
    作者:Zhuotao Tan、Chenjie Zhu、Jingwen Fu、Xiaowang Zhang、Ming Li、Wei Zhuang、Hanjie Ying
    DOI:10.1002/anie.201810881
    日期:2018.12.10
    novel strategy to regulate cofactor balance in vivo for whole‐cell biotransformation using a synthetic flavin analogue is reported. High efficiency, easy operation, and good applicability were observed for this system. Confocal laser scanning microscopy was employed to verify that the synthetic flavin analogue can directly permeate into Escherichia coli cells without modifying the cell membrane. This
    报道了一种使用合成黄素类似物调节全细胞生物转化体内辅因子平衡的新策略。观察到该系统的高效率,易于操作和良好的适用性。共聚焦激光扫描显微镜用于验证合成的黄素类似物可以直接渗透到大肠杆菌细胞中,而无需修饰细胞膜。这项工作提供了一种有前途的细胞内氧化还原调节方法,以构建更有效的细胞工厂。
  • N1,N10-Ethylene-bridged high-potential flavins: synthesis, characterization, and reactivity
    作者:Wen-Shan Li、Nanjing Zhang、Lawrence M Sayre
    DOI:10.1016/s0040-4020(01)00313-1
    日期:2001.5
    N-1,N-10-Ethyleneisoalloxazinium chloride and its 8-Cl-, 7-CF3-, and 3-CH3-7-CF3-substituted analogs were synthesized for the purpose of exhibiting thermal reactivity with organic substrates. The new flavins were characterized spectroscopically and electrochemically, and were found to react with amines, thiols, and phenylhydrazine, the latter case exhibiting catalytic aerobic recycling. Reactions of aliphatic benzylic and cyclopropyl amines with the 7-CF3 analog were also compared to their oxidations by tris(phenanthroline)iron(III). All reactions of the flavinium salts appear to occur through heterolytic rather than homolytic mechanisms. (C) 2001 Elsevier Science Ltd. All rights reserved.
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