2-Amino-1-(4-chlorophenyl)ethan-1-ol

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Company Name: Amatek Scientific Co. Ltd.  
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Company Name: ShangHai AmK Pharmaceutical Technology Co., Ltd.  
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2-Amino-1-(4-chlorophenyl)ethan-1-ol manufacturers

2-Amino-1-(4-chlorophenyl)ethan-1-ol Basic information
Product Name:2-Amino-1-(4-chlorophenyl)ethan-1-ol
Synonyms:2-Amino-1-(4-chlorophenyl)ethan-1-ol;AKOS BBV-002955;4-Chloro-beta-hydroxyphenethylamine 95%;2-Amino-1-(4-chlorophenyl)ethan-1-ol, 4-Chloro-beta-hydroxyphenethylamine;alpha-(Aminomethyl)-4-chlorobenzyl alcohol 95%;BENZENEMETHANOL, α-(AMINOMETHYL)-4-CHLORO-;alpha-(Aminomethyl)-4-chlorobenzylalcohol95%;alpha-(Aminomethyl)-4-chlorobenzyl alcohol
CAS:41870-82-0
MF:C8H10ClNO
MW:171.6241
EINECS:205-516-1
Product Categories:
Mol File:41870-82-0.mol
2-Amino-1-(4-chlorophenyl)ethan-1-ol Structure
2-Amino-1-(4-chlorophenyl)ethan-1-ol Chemical Properties
Melting point 93-96
Boiling point 319.8±27.0 °C(Predicted)
density 1.260±0.06 g/cm3(Predicted)
form powder
pka11.83±0.35(Predicted)
color white
Safety Information
HazardClass IRRITANT
HS Code 2922190090
MSDS Information
2-Amino-1-(4-chlorophenyl)ethan-1-ol Usage And Synthesis
Uses2-Amino-1-(4-chlorophenyl)ethanol is a useful synthetic intermediate in the synthesis of capsaicin analogs which exhibit potential analgesic activity. 2-Amino-1-(4-chlorophenyl)ethanol is also used as a reagent in the synthesis of imidazolyl arylamides as inhibitors of CYP24A1.
2-Amino-1-(4-chlorophenyl)ethan-1-ol Preparation Products And Raw materials
Tag:2-Amino-1-(4-chlorophenyl)ethan-1-ol(41870-82-0) Related Product Information
2-Hydroxysaclofen Hexaconazole Ketoconazole (+/-)-Ethyl-cis-[4-[[2-(2,4-dichlorophenyl)-2-(1H-imidazol-1-ylmethyl)-1,3-dioxolan-4-yl]-methylthio]phenyl]-carbamate hydrochloride ETACONAZOLE MICONAZOLE NITRATE Imazalil Econazole nitrate Propiconazole alpha-(2,4-Dichlorophenyl)-1H-imidazole-1-ethanol Vagistat Imazalil sulfate Dichloroisoproterenol hydrochloride CALMIDAZOLIUM CHLORIDE 2-(2,4-Dichlorophenyl)-2-(1H-imidazol-1-yl methyl)-1,3-dioxolane-4-methanol 3-(4-Chlorophenyl)-3-hydroxy-1-methyl-2-oxa-5-azoniaspiro[4.5]decane bromide 1,1-Bis(4-chlorophenyl)-2-[(4-methylbenzyl)amino]-1-ethanol 2-(4-Chlorophenyl)-4,4-diethyl-2-hydroxy-6-methyl-1,4-oxazinan-4-ium bromide