72800
4-Nitrobenzaldehyde
for spectrophotometric det. of amino sugars, ≥99.0%
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About This Item
Linear Formula:
O2NC6H4CHO
CAS Number:
Molecular Weight:
151.12
Beilstein:
386796
EC Number:
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.21
Quality Level
Assay
≥99.0% (HPLC)
≥99.0%
form
powder
quality
for spectrophotometric det. of amino sugars
technique(s)
UV/Vis spectroscopy: suitable
ign. residue
≤0.05%
mp
103-106 °C (lit.)
104-106 °C
SMILES string
[O-][N+](=O)c1ccc(C=O)cc1
InChI
1S/C7H5NO3/c9-5-6-1-3-7(4-2-6)8(10)11/h1-5H
InChI key
BXRFQSNOROATLV-UHFFFAOYSA-N
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Other Notes
Reagent for the spectrophotometric det. of amino carbohydrates
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Sens. 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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A. Nakamura et al.
Chemical & Pharmaceutical Bulletin, 17, 770-770 (1969)
Mikhail Yu Karganov et al.
Biological trace element research, 198(2), 567-574 (2020-03-08)
The objective of the present study was investigation of tissue trace element distribution in a streptozotocin model of DM1 in rats. DM1 was modeled in 2-month-old male Wistar rats (n = 30) using intraperitoneal injection of 45 mg/kg b.w. (STZ1) and 55 mg/kg b.w.
H Maheswaran et al.
Chemical communications (Cambridge, England), (39)(39), 4066-4068 (2006-10-07)
The dichloro[(-)-sparteine-N,N']copper(II) complex provides Henry adducts with high enantioselectivities (73-97% ee) in Henry reaction between nitromethane and various aldehydes.
Chao Li et al.
Journal of biotechnology, 150(4), 539-545 (2010-10-21)
Several proteases, especially pepsin, were observed to directly catalyze asymmetric aldol reactions. Pepsin, which displays well-documented proteolytic activity under acidic conditions, exhibited distinct catalytic activity in a crossed aldol reaction between acetone and 4-nitrobenzaldehyde with high yield and moderate enantioselectivity.
Anant Prakash et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 76(3-4), 356-362 (2010-04-27)
The new Schiff bases N,N'-bis (4-nitro benzaldehyde) ethylenediamine (L(1)) and N,N'-bis (acetophenone) ethylenediamine (L(2)) and its Zn(II), Cd(II) complexes were synthesized and characterized by different physicochemical studies. Vibrational spectra indicate coordination of metal ion through azomethine nitrogen and acetate/nitrate ions.
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