N,Alpha-Diphenyl Nitrone N-α-二苯硝酮
CAS 1137-96-8 MFCD00013895
化学结构图
SMILES: [O-]/[N+](=C\c1ccccc1)c1ccccc1
化学属性
| Mol. Formula | C13H11NO |
|---|---|
| Mol. Weight | 197.23 |
| Melting Point | 113-114° |
| TSCA | No |
别名和识别编码
| Chemical Name | N,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 Number | MFCD00013895 |
| CAS Number | 1137-96-8 |
| EC Number | 214-509-2 |
| Beilstein Registry Number | 608470 |
| Chemical Name Translation | N-α-二苯硝酮 |
| InChIKey | ZEAUJQWDPKRESH-KAMYIIQDSA-N |
| LabNetwork Molecule ID | LN04552096 |
| PubChem Substance ID | 3036381 |
| InChI | InChI=1S/C13H11NO/c15-14(13-9-5-2-6-10-13)11-12-7-3-1-4-8-12/h1-11H/b14-11- |
| Canonical SMILES | O=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).
