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N9608

Sigma-Aldrich

4′-Nitroacetophenone

98%

Synonym(s):

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

Linear Formula:
O2NC6H4COCH3
CAS Number:
100-19-6
Molecular Weight:
165.15
Beilstein:
607777
EC Number:
202-827-4
MDL number:
MFCD00007355
UNSPSC Code:
12352100
PubChem Substance ID:
24897904
NACRES:
NA.22

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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Related Categories

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Chemical radiosensitization of anoxic mammalian cells: effect of cell concentration.
D A Agnew et al.
Radiation research, 57(2), 246-259 (1974-02-01)
The effect of combinations of nitroaromatic and nitroxyl radiosensitizers on the radiation survival response of Chinese hamster cells, V.79-753B, in vitro.
B C Millar et al.
Radiation research, 88(2), 369-376 (1981-11-01)
Modification of radiation sensitivity of Bacillus megaterium spores by N2O and p-nitroacetophenone.
D Ewing et al.
Radiation research, 58(3), 481-488 (1974-06-01)
Katryn L Williams et al.
Journal of agricultural and food chemistry, 66(22), 5462-5472 (2018-05-15)
Benzobicyclon [3-(2-chloro-4-(methylsulfonyl)benzoyl)-2-phenylthiobicyclo[3.2.1]oct-2-en-4-one] is a pro-herbicide used against resistant weeds in California rice fields. Persistence of its active product, benzobicyclon hydrolysate, is of concern. As an acidic herbicide, the neutral species photolyzed faster than the more predominant anionic species ( t1/2
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
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