139351
3′-Aminoacetophenone
97%
Synonym(s):
3-Acetylaniline
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About This Item
Linear Formula:
H2NC6H4COCH3
CAS Number:
Molecular Weight:
135.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-722-3
Beilstein/REAXYS Number:
386009
MDL number:
Assay:
97%
Product Name
3′-Aminoacetophenone, 97%
InChI key
CKQHAYFOPRIUOM-UHFFFAOYSA-N
InChI
1S/C8H9NO/c1-6(10)7-3-2-4-8(9)5-7/h2-5H,9H2,1H3
SMILES string
CC(=O)c1cccc(N)c1
assay
97%
bp
289-290 °C (lit.)
mp
94-98 °C (lit.)
functional group
ketone
Quality Level
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Application
3′-Aminoacetophenone (3-Acetylaniline) was used as reagent during the asymmetric total synthesis of pactamycin. It was used as starting reagent during the synthesis of curcumin mimics with substituted sulfonyl group.
General description
3′-Aminoacetophenone acts as bifunctional coupling reagent during the synthesis of pyrimidines.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Chan Mug Ahn et al.
Bioorganic & medicinal chemistry letters, 19(5), 1481-1483 (2009-01-31)
In order to discover novel small vasodilatory molecules for potential use in the treatment of vascular disease, we tested the vasodilatation effect of two types of synthetic curcumin mimics, amide type (3) and sulfonyl amide type (4), upon the basilar
J S Früchtel et al.
Biotechnology and bioengineering, 71(2), 94-103 (2001-04-05)
A combination of symmetric building blocks and combinatorial functional group transformation for synthesis of pyrimidines was investigated. The purpose of the study was to maximize the return on invested synthetic efforts of reaction development for libraries. A representative set of
M K Subramanian et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 71(1), 59-67 (2008-01-08)
The gas phase infrared spectrum of 3-aminoacetophenone (3AAP) was measured in the range 5000-500 cm(-1) and with a resolution of 0.5 cm(-1). The Fourier transform Raman (FT-Raman) and Fourier transform infrared (FT-IR) spectra of 3AAP were recorded in the solid
Justin T Malinowski et al.
Science (New York, N.Y.), 340(6129), 180-182 (2013-04-13)
Medicinal application of many complex natural products is precluded by the impracticality of their chemical synthesis. Pactamycin, the most structurally intricate aminocyclopentitol antibiotic, displays potent antiproliferative properties across multiple phylogenetic domains, but it is highly cytotoxic. A limited number of
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