A38207
2-氨基苯乙酮 盐酸盐
99%
别名:
ω-氨基苯乙酮 盐酸盐, 苯甲酰甲胺 盐酸盐
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线性分子式:
C6H5COCH2NH2 · HCl
化学文摘社编号:
分子量:
171.62
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
226-787-2
Beilstein/REAXYS Number:
3563173
MDL number:
Assay:
99%
Form:
crystals
产品名称
2-氨基苯乙酮 盐酸盐, 99%
InChI key
CVXGFPPAIUELDV-UHFFFAOYSA-N
InChI
1S/C8H9NO.ClH/c9-6-8(10)7-4-2-1-3-5-7;/h1-5H,6,9H2;1H
SMILES string
Cl.NCC(=O)c1ccccc1
assay
99%
form
crystals
mp
194 °C (dec.) (lit.)
Quality Level
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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)
[Anorexigenic activity of various derivatives of alpha-aminoacetophenone].
M S Sánchez et al.
Archivos de farmacologia y toxicologia, 5(3), 165-168 (1979-12-01)
Yasumasa Iwai et al.
Chemical & pharmaceutical bulletin, 50(3), 441-443 (2002-03-26)
The new coupling reaction of phenacylamines with silylstannane and lithium diisopropylamide (LDA) is reported. The treatment of a phenacylamine iodide 1 with (trimethylsilyl)tributylstannane (Me3SiSnBu3) and cesium fluoride (CsF) gave a dimerization product 2 having no iodine atom. Reaction of 1
J B Mangold et al.
The Journal of biological chemistry, 259(12), 7772-7779 (1984-06-25)
Functionalization of the beta-carbon of phenethylamines has been shown to produce a new class of substrate/inhibitor of dopamine beta-monooxygenase. Whereas both beta-hydroxy- and beta- chlorophenethylamine are converted to alpha-aminoacetophenone at comparable rates, only the latter conversion is accompanied by concomitant
Frank Sporkert et al.
Forensic science international, 133(1-2), 39-46 (2003-05-14)
A sensitive and reproducible method for the quantitative determination of cathinone (CTN), norpseudoephedrine (NPE, cathine) and norephedrine (NE) from hair was developed. The compounds were extracted for 4 hours with phosphate buffer pH 2.0, followed by a standard solid phase
M J Bossard et al.
The Journal of biological chemistry, 265(10), 5640-5647 (1990-04-05)
A mechanism for beta-chlorophenethylamine inhibition of dopamine beta-monooxygenase has been postulated in which bound alpha-aminoacetophenone is generated followed by an intramolecular redox reaction to yield a ketone-derived radical cation as the inhibitory species (Mangold, J.B., and Klinman, J.P. (1984) J.
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