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72620

4′-Nitroacetophenone

purum, ≥97.0% (GC)

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About This Item

Linear Formula:
O2NC6H4COCH3
CAS Number:
100-19-6
Molecular Weight:
165.15
EC Number:
202-827-4
UNSPSC Code:
12352100
MDL number:
MFCD00007355
Beilstein/REAXYS Number:
607777
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grade

purum

assay

≥97.0% (GC)

bp

202 °C (lit.)

mp

75-78 °C (lit.), 76-80 °C

SMILES string

CC(=O)c1ccc(cc1)[N+]([O-])=O

InChI

1S/C8H7NO3/c1-6(10)7-2-4-8(5-3-7)9(11)12/h2-5H,1H3

InChI key

YQYGPGKTNQNXMH-UHFFFAOYSA-N

Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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K Tatsumi et al.
Journal of pharmacobio-dynamics, 4(2), 101-108 (1981-02-01)
The electron transfer mechanism in the reduction of aromatic nitro compounds by xanthine oxidase was investigated using methyl p-nitrobenzoate and p-nitroacetophenone as substrates. Methyl p-nitrobenzene was reduced by both one-electron and more than two-electron transfer mechanisms in the enzyme-electron donor
C M Krishna et al.
Indian journal of biochemistry & biophysics, 30(1), 7-9 (1993-02-01)
The photosensitizing properties of p-nitroacetophenone (PNAP), a well-known radiosensitizer, have been studied in near UV region. The mechanism of PNAP photosensitization has been investigated by testing the efficiency of singlet oxygen production using photooxidation of 2,2,6,6-tetramethylpiperidine (TEMP) and photodegradation of
N Cénas et al.
Archives of biochemistry and biophysics, 315(1), 170-176 (1994-11-15)
The study focused on the effects on various redox states of hemoglobin during NADPH: cytochrome P-450 reductase-catalyzed redox cycling of quinones and nitrocompounds. The following reactions involving quinone/semiquinone and methemoglobin/oxyhemoglobin redox couples were observed: (i) the direct oxidation of oxyhemoglobin
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Global Trade Item Number

SKUGTIN
CDS000533-1G04061825968001