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Merck
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Key Documents

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N9608

Sigma-Aldrich

4′-Nitroacetophenone

98%

Sinónimos:

1-(4-Nitrophenyl)ethan-1-one, 1-(4-Nitrophenyl)ethanone, 1-Acetyl-4-nitrobenzene, 4-Nitrophenyl methyl ketone, 4′-Nitroacetophenone, p-Acetylnitrobenzene

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About This Item

Fórmula lineal:
O2NC6H4COCH3
Número de CAS:
100-19-6
Peso molecular:
165.15
Beilstein/REAXYS Number:
607777
EC Number:
202-827-4
MDL number:
MFCD00007355
UNSPSC Code:
12352100
PubChem Substance ID:
24897904
NACRES:
NA.22

Quality Level

100

assay

98%

form

crystals

bp

202 °C (lit.)

mp

75-78 °C (lit.)

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

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Categorías relacionadas

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificados de análisis (COA)

Lot/Batch Number
WXBF3027V
BCCJ3440
BCCF8362
BCCC6077
BCBZ9552

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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
[Semiconservative and unscheduled DNA-synthesis of rat thymocytes under the influence of some radioprotecting and radiosensitizing agents (author's transl)].
K Tempel et al.
Strahlentherapie, 158(2), 112-122 (1982-02-01)
A Hissung et al.
International journal of radiation biology and related studies in physics, chemistry, and medicine, 39(1), 63-71 (1981-01-01)
The reactions of the one electron adduct of 2'-deoxyadenosine dA(-), in aqueous solutions have been studied using pulse radiolysis techniques with optical absorption and conductivity detection. The dA(-) radical anion itself shows a weak and featureless optical absorption at greater
J M Wong et al.
Pharmacogenetics, 3(2), 110-115 (1993-04-01)
The enzyme family carbonyl reductase, which catalyses the reduction of xenobiotic as well as endogenous ketones and aldehydes, has not been very well studied in terms of its biological functions and structural aspects. The aim of the present study was
N Iwata et al.
Biochemical pharmacology, 45(8), 1711-1714 (1993-04-22)
Interindividual variability of carbonyl reductase levels in human livers (N = 11) was examined by measuring reductase activity toward various substrates and by western blot analysis using anti-rat ovarian carbonyl reductase CR2 antibody. The carbonyl reductase activity toward p-nitrobenzaldehyde (PNBA)
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