InChI
1S/C9H9NO2/c1-8(10(11)12)7-9-5-3-2-4-6-9/h2-7H,1H3/b8-7+
SMILES string
[H]\C(=C(\C)[N+]([O-])=O)c1ccccc1
InChI key
WGSVFWFSJDAYBM-BQYQJAHWSA-N
assay
99%
form
solid
mp
63-65 °C (lit.)
functional group
amine, nitro, phenyl
storage temp.
2-8°C
Quality Level
General description
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。
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Spectroscopic (FT-IR, FT-Raman, UV and NMR) Investigation on 1-Phenyl-2-Nitropropene by Quantum Computational Calculations.
Xavier S and Periandy S.
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy (2015)
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)
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)
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.
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