V900695
4-Nitrobenzaldehyde
Vetec™, reagent grade, 98%
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About This Item
Linear Formula:
O2NC6H4CHO
CAS Number:
Molecular Weight:
151.12
EC Number:
209-084-5
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
386796
MDL number:
Assay:
98%
InChI key
BXRFQSNOROATLV-UHFFFAOYSA-N
InChI
1S/C7H5NO3/c9-5-6-1-3-7(4-2-6)8(10)11/h1-5H
SMILES string
[O-][N+](=O)c1ccc(C=O)cc1
grade
reagent grade
product line
Vetec™
assay
98%
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Legal Information
Vetec is a trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Sens. 1
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
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Jinmin Fan et al.
Chemical communications (Cambridge, England), (32)(32), 3792-3794 (2008-08-08)
Double-stranded DNA of natural origin can be used to facilitate nitro-aldol (or Henry) reaction in aqueous solution.
Jinmo Kim et al.
Analytical chemistry, 77(13), 4137-4141 (2005-07-01)
A chemical derivatization technique in time-of-flight secondary ion mass spectrometry (TOF-SIMS) has been developed to quantify the surface density of amine groups of plasma-polymerized ethylenediamine thin film deposited on a glass surface by inductively coupled plasma chemical vapor deposition. Chemical
Gang Wu et al.
The journal of physical chemistry. A, 112(5), 1024-1032 (2008-01-16)
We have used solid-state 17O NMR experiments to determine the 17O quadrupole coupling (QC) tensor and chemical shift (CS) tensor for the carbonyl oxygen in p-nitro-[1-(17)O]benzaldehyde. Analyses of solid-state 17O NMR spectra obtained at 11.75 and 21.15 T under both
Juan Qiao et al.
Talanta, 80(2), 770-776 (2009-10-20)
An innovative block copolymer capillary coating P(MAn-alt-St)(127)-b-PSt(592), synthesized by maleic anhydride and styrene, was developed as a new kind of coating for capillary electrophoresis. The covalent bond coating was effectively applied in the separation of raw material (4-nitrobenzaldehyde) and production
Mauro De Nisco et al.
The Journal of organic chemistry, 74(24), 9562-9565 (2009-11-27)
Dipeptides obtained from l-proline and beta(3)-l-amino acids are reported to catalyze enantioselective direct aldol reaction in aqueous medium, leading to significant anti:syn diastereomeric ratios and enantiomeric excesses. The simple introduction of a polar substituent at the C-2 position of the
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