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N9608

Sigma-Aldrich

4′-Nitroacetophenone

98%

Sinônimo(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

Fórmula linear:
O2NC6H4COCH3
Número CAS:
100-19-6
Peso molecular:
165.15
Beilstein:
607777
Número CE:
202-827-4
Número MDL:
MFCD00007355
Código UNSPSC:
12352100
ID de substância PubChem:
24897904
NACRES:
NA.22

Ensaio

98%

Formulário

crystals

p.e.

202 °C (lit.)

pf

75-78 °C (lit.)

cadeia de caracteres SMILES

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

chave InChI

YQYGPGKTNQNXMH-UHFFFAOYSA-N

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Categorias relacionadas

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

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Certificados de análise (COA)

Lot/Batch Number
BCCF8362
BCCC6077
BCBZ9552
MKCD7497
BCBS7839V

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G J Fisher et al.
Radiation research, 94(2), 231-238 (1983-05-01)
V-79 Chinese hamster fibroblasts in monolayer culture were exposed to ultraviolet radiation at 313, 334, 365, 380, and 405 nm in the presence of either misonidazole or para-nitroacetophenone, drugs which act as both photosensitizers and radiosensitizers of cell killing. Survival
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
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
C T Aravindakumar et al.
International journal of radiation biology, 66(4), 351-365 (1994-10-01)
The reactions of hydrated electrons e-aq with hypoxanthine and inosine were followed using pulse radiolysis methods. In a neutral solution the electron adduct of inosine is immediately protonated at the heteroatoms of the purine ring by water (k > 2.5
Wing-Yin Tsang et al.
Journal of the American Chemical Society, 131(39), 13952-13962 (2009-10-01)
Primary product isotope effects (PIEs) on L(+) and carboxylic acid catalyzed protonation of ring-substituted alpha-methoxystyrenes (X-1) to form oxocarbenium ions X-2(+) in 50/50 (v/v) HOH/DOD were calculated from the yields of the alpha-CH(3) and alpha-CH(2)D labeled ketone products, determined by
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