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About This Item
Linear Formula:
O2NC6H4CH=CHCHO
CAS Number:
Molecular Weight:
177.16
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
98%
form
solid
mp
140-143 °C (lit.)
functional group
aldehyde
nitro
storage temp.
2-8°C
SMILES string
[H]C(=O)\C=C\c1ccc(cc1)[N+]([O-])=O
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
General description
Reduction of trans-4-nitrocinnamaldehyde using the polymer-supported Hantzsch 1,4-dihydropyridine ester and a catalytic amount of HCl has been investigated.
Application
4-Nitrocinnamaldehyde has been used in the preparation of 2, 2′-[(E)-3-(4-nitrophenyl) prop-2-ene-1,1-diyl] bis(3-hydroxy-5, 5-dimethylcyclohex-2-en-1-one).
Signal Word
Warning
Hazard Statements
Precautionary 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
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Polymer-Supported Hantzsch 1, 4-Dihydropyridine Ester: An Efficient Biomimetic Hydrogen Source.
He R, et al.
Advanced Synthesis & Catalysis, 350(1), 54-60 (2008)
Joo Hwan Cha et al.
Acta crystallographica. Section E, Structure reports online, 68(Pt 8), o2510-o2510 (2012-08-21)
In the title compound, C(25)H(29)NO(6), each of the cyclo-hexenone rings adopts a half-chair conformation. The hy-droxy and carbonyl O atoms face each other and are oriented to allow for the formation of two intra-molecular O-H⋯O hydrogen bonds. In the crystal
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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