N9608
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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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
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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)
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)
Chemical radiosensitization of anoxic mammalian cells: effect of cell concentration.
D A Agnew et al.
Radiation research, 57(2), 246-259 (1974-02-01)
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
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