A38002
4′-Aminoacetophenone
99%
Synonym(s):
4-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:
202-801-2
Beilstein/REAXYS Number:
471493
MDL number:
Product Name
4′-Aminoacetophenone, 99%
InChI key
GPRYKVSEZCQIHD-UHFFFAOYSA-N
InChI
1S/C8H9NO/c1-6(10)7-2-4-8(9)5-3-7/h2-5H,9H2,1H3
SMILES string
CC(=O)c1ccc(N)cc1
assay
99%
form
powder
bp
293 °C (lit.)
mp
103-107 °C (lit.)
Quality Level
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Related Categories
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Regulatory Information
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V Mishra et al.
Pharmaceutica acta Helvetiae, 73(4), 215-218 (1998-12-23)
The thioureido derivative of 4-aminoacetophenone aryl semicarbazone have been prepared. These derivatives have been characterised on the basis of different physicochemical evidences. The anti-HIV-1 (HTLV-IIIB) and -HIV-2 (ROD) activity and cytotoxicity of the compounds were tested. The compound VII and
Dominik Cincić et al.
Acta crystallographica. Section C, Crystal structure communications, 64(Pt 4), o226-o229 (2008-04-09)
In the title compounds, 4-carboxyanilinium bromide, C(7)H(8)NO(2)(+) x Br(-), (I), and 4-acetylanilinium bromide, C(8)H(10)NO(+) x Br(-), (II), each asymmetric unit contains a discrete cation with a protonated amino group and a halide anion. Both crystal structures are characterized by two-dimensional
O A Aleksintseva et al.
Antibiotiki, 27(7), 493-495 (1982-01-01)
The effect of p-aminobenzoic acid on the biosynthesis of levorin was studied. It was shown that in the presence of exogenic p-aminobenzoic acid the antibiotic activity increased by 11 per cent. The acid added was transformed into p-aminoacetophenone which was
O A Aleksintseva et al.
Antibiotiki, 26(8), 566-570 (1981-08-01)
A method for spectrophotometric determination of p-aminoacetophenone (p-AAP) in the mycelium and fermentation broth filtrates of organisms producing polyenic macrolide antibiotics is described. The level of p-AAP accumulation was studied as applicable to the biosynthesis of levorin, a polyenic antibiotic
O Raatikainen et al.
Journal of chromatography, 585(2), 247-254 (1991-11-01)
A high-performance liquid chromatographic (HPLC) method for the determination of the aromaticity of heptaene polyene antibiotics has been developed. The released aromatic moiety of the heptaene polyenes aureofungin, candicidin, candimycin, hamycin and trichomycin was assayed after alkaline hydrolysis. The presence
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