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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
217-076-8
Beilstein/REAXYS Number:
1565424
MDL number:
Assay:
≥97.0% (T)
Form:
crystals
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
SMILES string
[O-][N+](=O)c1ccc(\C=C\C=O)cc1
grade
technical
assay
≥97.0% (T)
form
crystals
mp
139-142 °C
functional group
aldehyde, nitro
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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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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