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Merck
CN

424749

Sigma-Aldrich

1-苯基-2-硝基丙烯

99%

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About This Item

线性分子式:
C6H5CH=C(CH3)NO2
CAS号:
分子量:
163.17
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

99%

表单

solid

mp

63-65 °C (lit.)

官能团

amine
nitro
phenyl

储存温度

2-8°C

SMILES字符串

[H]\C(=C(\C)[N+]([O-])=O)c1ccccc1

InChI

1S/C9H9NO2/c1-8(10(11)12)7-9-5-3-2-4-6-9/h2-7H,1H3/b8-7+

InChI key

WGSVFWFSJDAYBM-BQYQJAHWSA-N

一般描述

反式-β-甲基-β-硝基苯乙烯(1-苯基-2-硝基丙烯),一种硝基苯乙烯衍生物,是 α,β-二取代的硝基烯烃。它是通过苯甲醛与硝基乙烷和丁胺反应合成的。使用 FT-IR、FT-Raman、NMR 和 UV 对 1-苯基-2-硝基丙烯进行了光谱分析。

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


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分析证书(COA)

Lot/Batch Number

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访问文档库

A Mori et al.
Chemical & pharmaceutical bulletin, 38(12), 3449-3451 (1990-12-01)
Microbial reduction of 1-phenyl-2-nitro-1-propene (3) was carried out using 57 strains of yeast, 40 strains of aerobic and facultatively anaerobic bacteria and 40 strains of strictly anaerobic bacteria. Nine strains of yeast (Candida tropicalis, etc.,) had the ability to reduce
Organocatalytic diastereo- and enantioselective sulfa-Michael addition to α,β-disubstituted nitroalkenes
Pei QL, et al.
Tetrahedron, 69, 5367-5373 (2013)
Tundo P and Andraos J
Green Syntheses, 119-119 (2014)
Diego Romano et al.
Microbial cell factories, 13, 60-60 (2014-04-29)
Old Yellow Enzymes (OYEs) are flavin-dependent enoate reductases (EC 1.6.99.1) that catalyze the stereoselective hydrogenation of electron-poor alkenes. Their ability to generate up to two stereocenters by the trans-hydrogenation of the C = C double bond is highly demanded in asymmetric synthesis.
Gas chromatographic and mass spectral analysis of amphetamine products synthesized from 1-phenyl-2-nitropropene.
DeRuiter J, et al.
Journal of Chromatographic Science, 32(11), 511-519 (1994)

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