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2-methyl-2-(pent-4-en-1-yl)-3-phenyl-2H-azirine | 62901-83-1

中文名称
——
中文别名
——
英文名称
2-methyl-2-(pent-4-en-1-yl)-3-phenyl-2H-azirine
英文别名
2-Methyl-2-(4-pentenyl)-3-phenyl-2H-azirin;2-methyl-2-pent-4-enyl-3-phenyl-2H-azirine;2-Methyl-2-(pent-4-en-1-yl)-3-phenyl-2H-azirene;2-methyl-2-pent-4-enyl-3-phenylazirine
2-methyl-2-(pent-4-en-1-yl)-3-phenyl-2H-azirine化学式
CAS
62901-83-1
化学式
C14H17N
mdl
——
分子量
199.296
InChiKey
ZUEFKQDTHZVEJD-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):
    3.6
  • 重原子数:
    15
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    12.4
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    2-methyl-2-(pent-4-en-1-yl)-3-phenyl-2H-azirine 在 sodium hydride 作用下, 以 为溶剂, 反应 111.0h, 生成 1,2-dimethyl-7,9-diphenyl-8-azatricyclo<4.3.1.02,7>dec-8-ene
    参考文献:
    名称:
    Intramolecular Diels-Alder reactions of 3H-pyrroles resulting from thermal rearrangements of 2H-pyrroles
    摘要:
    DOI:
    10.1021/jo00234a009
  • 作为产物:
    描述:
    trimethyl-[(E)-(2-methyl-1-phenylhept-6-enylidene)amino]azanium;iodide 以87%的产率得到
    参考文献:
    名称:
    EDDAIF, ABDELHAMID;LAURENT, ANDRE;MISON, PIERRE;PELLISSIER, NICOLE;CARRUP+, J. ORG. CHEM., 52,(1987) N 25, 5548-5560
    摘要:
    DOI:
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文献信息

  • Visible-Light Promoted Selective Imination of Unactivated C–H Bonds via Copper-nitrene Intermediates for the Synthesis of 2<i>H</i>-Azirines
    作者:Liyan Feng、Chao Yang、Wujiong Xia
    DOI:10.1021/acs.orglett.9b03103
    日期:2019.10.18
    strategy to trap iminyl radicals with copper ions has been developed at room temperature, the resulted high-valent Cu(III) imine intermediate resets quickly to form nitrene and then to furnish a 2H-azirine. This protocol with dual copper/photoredox catalyst enables the selective imination of unactivated C-H bonds under mild conditions with a broader scope. Moreover, this method also uncovers a novel ring-expansion
    在室温下开发了一种用离子捕获亚胺基的新策略,所得的高价Cu(III)亚胺中间体迅速复位,形成亚硝基,然后提供2H-叠氮基。带有双/光氧化还原催化剂的该方案能够在较宽的范围内在温和条件下选择性活化未活化的CH键。此外,该方法还揭示了由环丁基生物产生α-酰基环戊烷酮的新的扩环重排。
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同类化合物

[(2S)-3-苯基-2H-氮杂环丙烯-2-基]甲醇 3-苯基-2H-氮丙啶-2-甲醛 3-(4-硝基苯基)-2H-吖丙因 3-(4-甲基苯基)-2H-吖丙因-2-甲醛 2H-氮丙啶 2-甲基-3-苯基-2H-吖丙因-2-甲醛 1H-氮丙啶 1-(3-苯基-2H-氮杂环丙烯-2-基)乙酮 (3-苯基-2H-氮杂环丙烯-2-基)甲醇 2-benzyl-3-phenyl-2H-azirine phenyl 3-phenyl-2H-aziren-2-ylsulfide <(3'-phenyl-2'H-azirin-2'-yl)methyl>phosphonic acid diethyl ester 3-(4-(tert-butyl)phenyl)-2H-azirine 3-phenyl-2H-azirine-2-methanol 3-Methyl-2-(4-nitrophenyl)-2H-azirine 3-(4-bromophenyl)-2H-azirine-2-carboxaldehyde 4-methoxy-N-(3-phenyl-2H-azirin-2-ylmethylene)-aniline 3-(3-Methoxyphenyl)-2,2-dimethyl-2H-azirene 3-(o-chlorophenyl)-2,2-dimethyl-2H-azirine 2-(3-chlorophenyl)-3-methyl-2H-azirine-2-carbonitrile (E)-3-(3-Phenyl-2H-azirin-2-yl)-propenal 3-Methyl-2-phenylazirin (E)-2-(2-Butenyl)-2-methyl-3-phenyl-2H-azirin 2-methyl-2-(3-methyl-2-butenyl)-3-phenyl-2H-azirine methyl-2,phenyl-2,ethyl-3 aziridine 3-but-3-enyl-2-methyl-2-phenyl-2H-azirine 2,3-dimethyl-2-phenyl-2H-azirine 2,2-dimethyl-3-(4-t-butylphenyl)-2H-azirine 2-Methyl-2-methallyl-3-phenyl-2H-azirin methyl 2-(2-methoxy-6-methylphenyl)-2H-azirine-3-carboxylate 2-[3-(3-bromophenyl)-2H-azirin-2-yl]-5-(trifluoromethyl)pyridine ethyl 2-(2-methoxyphenyl)-2H-azirine-3-carboxylate 3-(4-fluorophenyl)-2-(2-(5-trifluoromethyl)pyridyl)-2H-azirine (E)-1-Phenyl-3-(3-phenyl-2H-azirin-2-yl)-propenone 2-bromo-3-phenyl-2-phenylsulfonylmethyl-2H-azirine 2-cyano-2H-azirene diethyl(3-phenyl-2-H-azirin-2-yl) phosphonate diethyl(-)-S-(3-phenyl-2-H-azirin-2-yl) phosphonate 2-methyl-3-phenyl-2-(2-phenylethyl)azirine (butene-3'yl)-2 methyl-2 phenyl-3 2H-azirine 2-methyl-2-(pent-4-en-1-yl)-3-phenyl-2H-azirine 2-(Dimethoxymethyl)-3-phenyl-2H-azirin 3-(4-methoxyphenyl)-2H-azirine-2-carbaldehyde methyl 2-(2,3,4-trimethoxy-6-methylphenyl)-2H-azirine-3-carboxylate 2-(2-bromophenyl)-3-methyl-2H-azirine 2-(2,4-dimethylphenyl)azirine 3-methyl-2-o-tolyl-2H-azirine-2-carbonitrile 2-azido-2-formyl-3-phenyl-2H-azirine 2,3-dimethyl-1H-azirine 2-(4-fluorophenyl)-3-methyl-2H-azirine-2-carbonitrile