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
UNSPSC Code:
12352200
NACRES:
NA.21
PubChem Substance ID:
EC Number:
209-084-5
Beilstein/REAXYS Number:
386796
MDL number:
Assay:
≥99.0% (HPLC), ≥99.0%
Form:
powder
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
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%
Quality Level
mp
104-106 °C
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Other Notes
Reagent for the spectrophotometric det. of amino carbohydrates
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
ppe
dust mask type N95 (US), Eyeshields, Faceshields, 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.
Amit A Kudale et al.
The Journal of organic chemistry, 73(21), 8437-8447 (2008-09-30)
Condensation of 3-aminocoumarin (5) with 4-nitrobenzaldehyde (8) afforded a 2-azadiene (9), which reacted with various electron-rich alkenes (10 examples) in the presence of Yb(OTf)3 to afford 1,2,3,4-tetrahydropyrido[2,3-c]coumarins. Yields were generally good, but the diastereomeric ratios were highly variable. The products
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