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74115

Sigma-Aldrich

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:
1565424
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

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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