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5 G
$78.04
About This Item
Linear Formula:
C6H5CH=C(CH3)NO2
CAS Number:
Molecular Weight:
163.17
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
$78.04
List Price$84.10Save 7%Web-Only Promotion
Available to ship onApril 17, 2025Details
Request a Bulk Order
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assay
99%
form
solid
mp
63-65 °C (lit.)
functional group
amine
nitro
phenyl
storage temp.
2-8°C
SMILES string
[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
Related Categories
General description
trans-β-Methyl-β-nitrostyrene (1-phenyl-2-nitropropene), a nitrostyrene derivative is an α,β-disubstituted nitroalkene.[1] It has been synthesized by reacting benzaldehyde with nitroethane and butylamine.[2] Spectroscopic analysis of 1-phenyl-2-nitropropene has been done using FT-IR, FT-Raman, NMR and UV.[3]
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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)
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
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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