N-(2-Aminoethyl)-4-chlorobenzamide hydrochloride

N-(2-Aminoethyl)-4-chlorobenzamide hydrochloride Suppliers list
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: 3B Pharmachem (Wuhan) International Co.,Ltd.  
Tel: 18930552037
Email: 3bsc@sina.com
Company Name: Chemsky(shanghai)International Co.,Ltd.  
Tel: 021-50135380
Email: shchemsky@sina.com
Company Name: ShangHai AmK Pharmaceutical Technology Co., Ltd.  
Tel: 微信 18019252918 18019252918
Email: sale@amkchem.com
Company Name: Zhengzhou Guancheng Laboratory equipment Sales  
Tel: 0371-88888888 qq272369594;2159423853qq
Email: 2723695949@qq.com
N-(2-Aminoethyl)-4-chlorobenzamide hydrochloride Basic information
Product Name:N-(2-Aminoethyl)-4-chlorobenzamide hydrochloride
Synonyms:N-(2-AMINOETHYL)-4-CHLOROBENZAMIDE HCL;Zinc02555368;RO 16-6491;N-(2-Aminoethyl)-4-chlorobenzamide hydrochloride
CAS:94319-79-6
MF:C9H12Cl2N2O
MW:235.11
EINECS:
Product Categories:Heterocyclic Compounds;Inhibitors;Neurochemicals;Amines;Aromatics
Mol File:94319-79-6.mol
N-(2-Aminoethyl)-4-chlorobenzamide hydrochloride Structure
N-(2-Aminoethyl)-4-chlorobenzamide hydrochloride Chemical Properties
Melting point 209-210°C
storage temp. Refrigerator
solubility H2O: soluble
form solid
color white
Stability:Store in Freezer at -20°C
Safety Information
WGK Germany 3
MSDS Information
ProviderLanguage
SigmaAldrich English
N-(2-Aminoethyl)-4-chlorobenzamide hydrochloride Usage And Synthesis
Chemical PropertiesWhite Solid
UsesA competitive, time-dependent reversible inhibitor of monamine oxidase-B (MAO-B) is also an analogue of N-(2-Aminoethyl)benzamide.
UsesN-(2-Aminoethyl)-4-chlorobenzamide Hydrochloride is a competitive, time-dependent reversible inhibitor of monamine oxidase-B (MAO-B) and an analogue of N-(2-Aminoethyl)benzamide (1,2).
N-(2-Aminoethyl)-4-chlorobenzamide hydrochloride Preparation Products And Raw materials
Tag:N-(2-Aminoethyl)-4-chlorobenzamide hydrochloride(94319-79-6) Related Product Information
LORGLUMIDE N-(2-Aminoethyl)-4-chlorobenzamide hydrochloride Ethyl 2-[1-(2,4-dichlorobenzoyl)-3-oxo-2-piperazinyl]acetate 3,4-Dichloro-N-(2-[(2-hydroxyethyl)amino]-2-oxoethyl)benzenecarboxamide 4-(4-Chlorobenzoyl)-1-(4-chlorobenzyl)-3-methyl-3,4-dihydro-2(1H)-quinoxalinone N-(2-[(3,4-Dichlorobenzoyl)amino]ethyl)-2,5-bis(2,2,2-trifluoroethoxy)benzenecarboxamide N-(2-[(2,4-Dichlorobenzoyl)amino]ethyl)-2,5-bis(2,2,2-trifluoroethoxy)benzenecarboxamide 3,4-Dichloro-N-(2-[4-(4-chlorophenyl)piperazino]-2-oxoethyl)benzenecarboxamide (8-[3-Chloro-5-(trifluoromethyl)-2-pyridinyl]-3,3-dimethyl-1,4,8-triazaspiro[4.5]dec-1-yl)(2,4-dichlorophenyl)methanone Ethyl 2-[1-(3,4-dichlorobenzoyl)-3-oxo-2-piperazinyl]acetate N-[5-Acetyl-1-(4-chlorobenzyl)-6-methyl-2-oxo-1,2-dihydro-3-pyridinyl]-4-chlorobenzenecarboxamide 3,4-Dichloro-N-[1-(2,6-dichlorobenzyl)-2-oxo-1,2-dihydro-3-pyridinyl]benzenecarboxamide 4-Chloro-N-[1-(2-([3-chloro-5-(trifluoromethyl)-2-pyridinyl]amino)ethyl)-2,5-dioxo-1,2,5,6,7,8-hexahydro-3-quinolinyl]benzenecarboxamide 2,4-Dichloro-N-[1-(2,6-dichlorobenzyl)-2-oxo-1,2-dihydro-3-pyridinyl]benzenecarboxamide (4-Chlorophenyl)[4-(6-chloro-2-pyridinyl)piperazino]methanone 4-Chloro-N-(2-([3-chloro-5-(trifluoromethyl)-2-pyridinyl]amino)ethyl)benzenecarboxamide 4-Chloro-N-(2-[2-(4-([3-chloro-5-(trifluoromethyl)-2-pyridinyl]amino)butanoyl)hydrazino]-2-oxoethyl)benzenecarboxamide 4-Chloro-N-[1-(2,6-dichlorobenzyl)-2-oxo-1,2-dihydro-3-pyridinyl]benzenecarboxamide