N9608
4′-硝基苯乙酮
98%
别名:
1-(4-硝基苯基)-1-乙酮, 1-(4-硝基苯基)乙酮, 1-乙酰基-4-硝基苯, 4′-硝基苯乙酮, 4-硝基苯甲酮, 对乙酰基硝基苯
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关于此项目
线性分子式:
O2NC6H4COCH3
化学文摘社编号:
分子量:
165.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-827-4
Beilstein/REAXYS Number:
607777
MDL number:
Assay:
98%
Form:
crystals
InChI key
YQYGPGKTNQNXMH-UHFFFAOYSA-N
InChI
1S/C8H7NO3/c1-6(10)7-2-4-8(5-3-7)9(11)12/h2-5H,1H3
SMILES string
CC(=O)c1ccc(cc1)[N+]([O-])=O
assay
98%
form
crystals
bp
202 °C (lit.)
mp
75-78 °C (lit.)
Quality Level
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
[Semiconservative and unscheduled DNA-synthesis of rat thymocytes under the influence of some radioprotecting and radiosensitizing agents (author's transl)].
K Tempel et al.
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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
J M Wong et al.
Pharmacogenetics, 3(2), 110-115 (1993-04-01)
The enzyme family carbonyl reductase, which catalyses the reduction of xenobiotic as well as endogenous ketones and aldehydes, has not been very well studied in terms of its biological functions and structural aspects. The aim of the present study was
A Hissung et al.
International journal of radiation biology and related studies in physics, chemistry, and medicine, 39(1), 63-71 (1981-01-01)
The reactions of the one electron adduct of 2'-deoxyadenosine dA(-), in aqueous solutions have been studied using pulse radiolysis techniques with optical absorption and conductivity detection. The dA(-) radical anion itself shows a weak and featureless optical absorption at greater
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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