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Key Documents

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:
Molecular Weight:
165.15
Beilstein:
607777
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

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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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

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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)
Y G Smeyers et al.
International journal of radiation biology and related studies in physics, chemistry, and medicine, 39(6), 649-653 (1981-06-01)
The electron affinity of eight well-known nitroaromatic and nitroheterocyclic radiosensitizers is computed resorting to a quantum mechanical approach. Four of the compounds studied were nitroimidazoles; but p-nitroacetophenone and some 5-nitrofuran derivatives were also investigated for comparison. A good correlation between
K Washino et al.
International journal of radiation biology and related studies in physics, chemistry, and medicine, 41(3), 271-282 (1982-03-01)
Native calf thymus DNA, denatured DNA, and synthetic nucleic acids (poly A, poly C, poly U, and poly G) crosslink upon irradiation with 16 MeV electrons in O2-free dilute aqueous solutions containing 0.5mol/l t-butanol and p-nitroacetophenone (PNAP) or nitrobenzene at

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