N,Alpha-Diphenyl Nitrone N-α-二苯硝酮

CAS 1137-96-8 MFCD00013895

化学结构图

1137-96-8
SMILES: [O-]/[N+](=C\c1ccccc1)c1ccccc1

化学属性

Mol. FormulaC13H11NO
Mol. Weight197.23
Melting Point113-114°
TSCANo

别名和识别编码

Chemical NameN,Alpha-Diphenyl Nitrone
Synonym (Z)-N,1-Diphenylmethanimine oxide {LY} (Z)-N,1-Diphenylmethanimine oxide {} {LY} (Z)-N,1-Diphenylmethanimine oxide {} {} {LY} (Z)-N,1-Diphenylmethanimine oxide {} {} {} {LY} (Z)-N,1-Diphenylmethanimine oxide {} {} {} {} {LY} (Z)-N,1-Diphenylmethanimine oxide {} {} {} {} {} {LY} (Z)-N,1-Diphenylmethanimine oxide {} {} {} {} {} {} {LY} (Z)-N,1-Diphenylmethanimine oxide {} {} {} {} {} {} {} {LY} (Z)-N,1-Diphenylmethanimine oxide {} {} {} {} {} {} {} {} {LY} (Z)-N,1-Diphenylmethanimine oxide {} {} {} {} {} {} {} {} {} {LY} (Z)-N,1-Diphenylmethanimine oxide {} {} {} {} {} {} {} {} {} {} {LY} (Z)-N,1-Diphenylmethanimine oxide {} {} {} {} {} {} {} {} {} {} {} {LY} (Z)-N,1-Diphenylmethanimine oxide {} {} {} {} {} {} {} {} {} {} {} {} {LY} (Z)-N,1-Diphenylmethanimine oxide {} {} {} {} {} {} {} {} {} {} {} {} {} {LY} (Z)-N,1-Diphenylmethanimine oxide {} {} {} {} {} {} {} {} {} {} {} {} {} {} {LY} (Z)-N,1-Diphenylmethanimine oxide {} {} {} {} {} {} {} {} {} {} {} {} {} {} {
MDL NumberMFCD00013895
CAS Number1137-96-8
EC Number214-509-2
Beilstein Registry Number608470
Chemical Name TranslationN-α-二苯硝酮
InChIKeyZEAUJQWDPKRESH-KAMYIIQDSA-N
LabNetwork Molecule IDLN04552096
PubChem Substance ID3036381
InChIInChI=1S/C13H11NO/c15-14(13-9-5-2-6-10-13)11-12-7-3-1-4-8-12/h1-11H/b14-11-
Canonical SMILESO=N(=CC=1C=CC=CC1)C=2C=CC=CC2
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分类

  • {uni_hamburg}

相关文献及参考

  • Short: IV/7b Title: Liquid Crystals: Two-Ring Systems with Bridging Group Author: Vill, V. Editor: Thiem, J. Source: Landolt-Börnstein, New Series Volume: IV/7b Year: 1992 Keyword: organic compounds; enthaly of fusion; melting point; phase transition; liquid crystals; glass transition ISBN: 3-540-55504-8 ISBN: 978-3-540-55504-9 Internet Resource: DOI:10.1007/b46099 RefComment: 10 figs., VIII, 653 pages.
  • For an example of 1,3-dipolar cycloaddition with an alkene to give an isoxazolidine, see: Org. Synth. Coll., 5, 1124 (1973):
  • Similarly, regioselective addition to propiolic esters or alkynyl ketones gives isoxazolines: Tetrahedron, 44, 1247 (1988). The regioselectivity of 1,3-dipolar additions of nitrones with electron-deficient alkenes has been studied: J. Org. Chem., 49, 276 (1984).
  • Reviews: 1,3-Dipolar cycloadditions of nitrones: Synthesis, 205 (1975); The [3+2] nitrone-olefin cycloaddition reaction: Org. React., 36, 1 (1988); Synthetic applications of nitrones: Org. Prep. Proced. Int., 17, 25 (1985).

安全信息

Storage condition

系列性分类

  1. Functional Group 官能团索引
  2. N-oxide

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