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A38207

Sigma-Aldrich

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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1 G
$70.20
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$152.00

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1 G
$70.20
5 G
$152.00

About This Item

线性分子式:
C6H5COCH2NH2 · HCl
CAS号:
5468-37-1
分子量:
171.62
Beilstein:
3563173
EC 号:
226-787-2
MDL编号:
MFCD00012873
UNSPSC代码:
12352100
PubChem化学物质编号:
24890815
NACRES:
NA.22

$70.20

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方案

99%

表单

crystals

mp

194 °C (dec.) (lit.)

SMILES字符串

Cl.NCC(=O)c1ccccc1

InChI

1S/C8H9NO.ClH/c9-6-8(10)7-4-2-1-3-5-7;/h1-5H,6,9H2;1H

InChI key

CVXGFPPAIUELDV-UHFFFAOYSA-N

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相关类别

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCBB3937
BCBB3937V
1292912
09720KH
05723BH

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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
Dopamine beta-hydroxylase: activity and inhibition in the presence of beta-substituted phenethylamines.
J P Klinman et al.
Biochemistry, 21(1), 67-75 (1982-01-05)
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.
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
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