Skip to Content
Merck
CN

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

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
O2NC6H4COCH3
CAS Number:
100-19-6
Molecular Weight:
165.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24897904
EC Number:
202-827-4
Beilstein/REAXYS Number:
607777
MDL number:
MFCD00007355

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

4′-Nitroacetophenone, 98%

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

100

Looking for similar products? Visit Product Comparison Guide

Related Categories

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
WXBF6262V
WXBF3027V
BCCJ3440
BCCF8362
BCCC6077

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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
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
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
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
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service