74115
trans-4-Nitrocinnamaldehyde
technical, ≥97.0% (T)
Synonym(s):
trans-3-(4-Nitrophenyl)-2-propenal
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About This Item
Empirical Formula (Hill Notation):
C9H7NO3
CAS Number:
Molecular Weight:
177.16
Beilstein/REAXYS Number:
1565424
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
grade
technical
assay
≥97.0% (T)
form
crystals
mp
139-142 °C
SMILES string
[O-][N+](=O)c1ccc(\C=C\C=O)cc1
InChI
1S/C9H7NO3/c11-7-1-2-8-3-5-9(6-4-8)10(12)13/h1-7H/b2-1+
InChI key
ALGQVMMYDWQDEC-OWOJBTEDSA-N
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Certificates of Analysis (COA)
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E Eder et al.
Mutagenesis, 6(4), 261-269 (1991-07-01)
Seventeen cinnamaldehydes, cinnamic acids, 2-furylacroleins and related compounds were tested in the Salmonella preincubation reversion assay and in the SOS chromotest. Of eight compounds containing nitrogroups, seven were clearly mutagenic in the presence of S9 mix and six in its
I Baburina et al.
Biochemistry, 37(5), 1245-1255 (1998-03-07)
The residue C221 on pyruvate decarboxylase (EC. 4.1.1.1) from Saccharomyces cerevisiae has been shown to be the site where the substrate activation cascade is triggered [Baburina et al. (1994) Biochemistry 33, 5630-5635] and is located on the beta domain [Arjunan
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