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3-CHLORO-4-METHOXYBENZYLAMINE HYDROCHLORIDE

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CAS:41965-95-1
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3-CHLORO-4-METHOXYBENZYLAMINE HYDROCHLORIDE manufacturers

3-CHLORO-4-METHOXYBENZYLAMINE HYDROCHLORIDE Basic information
Product Name:3-CHLORO-4-METHOXYBENZYLAMINE HYDROCHLORIDE
Synonyms:BIO-FARMA BF004393;3-chloro-4-methoxybenzylamine, HC;4-AMINOMETHYL-2-CHLOROANISOLE HCL;4-AMINOMETHYL-2-CHLOROANISOLE HYDROCHLORIDE;3-chloro-4-methoxybenzylamineHCl;3-Chloro-4-methoxybenzylamineHCl95%;3-Chloro-4-methoxybenzylaminehydrochloride95%;3-Chloro-4-methoxybenzylamine hydrochloride 95%
CAS:41965-95-1
MF:C8H11Cl2NO
MW:208.09
EINECS:609-972-6
Product Categories:Anilines, Aromatic Amines and Nitro Compounds;pharmacetical;Anilines, Amides & Amines;Anisoles, Alkyloxy Compounds & Phenylacetates;Chlorine Compounds;Benzene derivatives;Amine Salts;Nitrogen Compounds;Organic Building Blocks;41965-95-1
Mol File:41965-95-1.mol
3-CHLORO-4-METHOXYBENZYLAMINE HYDROCHLORIDE Structure
3-CHLORO-4-METHOXYBENZYLAMINE HYDROCHLORIDE Chemical Properties
Melting point 250-255 °C (lit.)
storage temp. Inert atmosphere,Room Temperature
solubility soluble in Methanol
form Solid
color White to Almost white
InChIInChI=1S/C8H10ClNO.ClH/c1-11-8-3-2-6(5-10)4-7(8)9;/h2-4H,5,10H2,1H3;1H
InChIKeyIKWWOZCEHOYKAO-UHFFFAOYSA-N
SMILESNCC1=CC=C(OC)C(Cl)=C1.[H]Cl
CAS DataBase Reference41965-95-1(CAS DataBase Reference)
Safety Information
Hazard Codes T
Risk Statements 25-37/38-41
Safety Statements 26-36/37-45-39
RIDADR UN 2811 6.1/PG 3
WGK Germany 3
Hazard Note Toxic
HazardClass IRRITANT
HazardClass 6.1
HS Code 2922290090
MSDS Information
ProviderLanguage
SigmaAldrich English
3-CHLORO-4-METHOXYBENZYLAMINE HYDROCHLORIDE Usage And Synthesis
Chemical PropertiesWhite powder solid
Synthesis
4-Methoxybenzylamine

2393-23-9

3-CHLORO-4-METHOXYBENZYLAMINE HYDROCHLORIDE

41965-95-1

General procedure for the synthesis of 3-chloro-4-methoxybenzylamine hydrochloride from 4-methoxybenzylamine: acetic acid (100 ml) was slowly added to 4-methoxybenzylamine (100 g) at 25-30 °C. Subsequently, additional acetic acid (750 ml) was added to the reaction mixture. Sulfonyl chloride (87.84 ml) was slowly added dropwise to the reaction mixture at 20-25 °C and stirred continuously for 6 h at the same temperature. After completion of the reaction, methyl tert-butyl ether (850 ml) was added to the reaction mixture at 25-30 °C. The reaction mixture was cooled to 15-20°C and stirring was continued at this temperature for 1 hour. The precipitated solid product was filtered, washed with methyl tert-butyl ether and dried to give 3-chloro-4-methoxybenzylamine hydrochloride. Yield: 118 g.

References[1] Synthesis, 2003, # 3, p. 403 - 407
[2] Synthetic Communications, 2000, vol. 30, # 14, p. 2609 - 2612
[3] Tetrahedron, 2003, vol. 59, # 35, p. 6991 - 7009
[4] Organic letters, 2001, vol. 3, # 25, p. 4063 - 4066
[5] Patent: WO2015/1567, 2015, A1. Location in patent: Page/Page column 21
Tag:3-CHLORO-4-METHOXYBENZYLAMINE HYDROCHLORIDE(41965-95-1) Related Product Information
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