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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All Photos(3)
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
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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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Modification of radiation sensitivity of Bacillus megaterium spores by N2O and p-nitroacetophenone.
D Ewing et al.
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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)
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
H B Michaels
International journal of radiation oncology, biology, physics, 12(7), 1055-1058 (1986-07-01)
The oxygen concentration in stirred aqueous solutions contained in sealed glass vessels was continuously monitored during irradiation with a sensitive Clark-type oxygen probe. The yield of radiolytic oxygen depletion, g(-O2), in alpha medium was determined to be about 0.44 microM/Gy
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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