3567-82-6

Basic information

• Product Name: alpha-(aminomethyl)-3,4-dichlorobenzyl alcohol
• Synonyms: alpha-(aminomethyl)-3,4-dichlorobenzyl alcohol;3,4-dichlorophenylethanolamine;α-(Aminomethyl)-3,4-dichlorobenzenemethanol;3672-26-2 (Hydrochloride);Einecs 222-659-5;2-AMino-1-(3,4-dichlorophenyl)ethanol HCl;2-Amino-1-(3,4-dichloro-phenyl)-ethanol;Benzenemethanol, a-(aminomethyl)-3,4-dichloro-
• CAS NO: 3567-82-6
• Molecular Formula: C₈H₉Cl₂NO
• Molecular Weight: 206.06916
• EINECS: 222-659-5
• Mol File: 3567-82-6.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 354.1°Cat760mmHg
• Flash Point: 167.9°C
• Appearance: /
• Density: g/cm³
• Vapor Pressure: 1.26E-05mmHg at 25°C
• Refractive Index: 1.6
• CAS DataBase Reference: alpha-(aminomethyl)-3,4-dichlorobenzyl alcohol(CAS DataBase Reference)
• NIST Chemistry Reference: alpha-(aminomethyl)-3,4-dichlorobenzyl alcohol(3567-82-6)
• EPA Substance Registry System: alpha-(aminomethyl)-3,4-dichlorobenzyl alcohol(3567-82-6)

Safety Data

• Hazardous Substances Data: 3567-82-6(Hazardous Substances Data)

Usage

General Description

Alpha-(aminomethyl)-3,4-dichlorobenzyl alcohol is a chemical compound with the molecular formula C9H10Cl2NO and a molecular weight of 225.09 g/mol. It is a derivative of 3,4-dichlorobenzyl alcohol and contains an aminomethyl group attached to the alpha carbon. alpha-(aminomethyl)-3,4-dichlorobenzyl alcohol is mainly used as an antifungal and antibacterial agent in various pharmaceutical and personal care products. It is known for its effective antimicrobial properties, making it a common ingredient in mouthwashes, skin cleansers, and topical antiseptics. Additionally, alpha-(aminomethyl)-3,4-dichlorobenzyl alcohol has also been studied for its potential as a therapeutic agent in the treatment of various infections and diseases.

InChI:InChI=1/C8H9Cl2NO/c9-6-2-1-5(3-7(6)10)8(12)4-11/h1-3,8,12H,4,11H2

Upstream product

• 380650-10-2 2-amino-1-(3,4-dichloro-phenyl)-ethanone 
• 53065-95-5 2-chloro-1-(3,4-dichlorophenyl)ethan-1-ol 
• 6287-38-3 3,4-dichlorobenzaldehyde 
• 958452-69-2 (3,4-dichloro-phenyl)-glyoxal-2-oxime 
• 95-50-1 1,2-dichloro-benzene 
• 2642-63-9 3',4'-dichloroacetophenone 
• 42981-08-8 2,3',4'-trichloroacetophenone 
• 41995-19-1 2-amino-1-(3,4-dichloro-phenyl)-ethanone; hydrochloride 
• 2632-10-2 2-bromo-1-(3,4-dichlorophenyl)ethanone 

Downstream Products

• 68287-28-5 1-(3,4-dichloro-phenyl)-2-(1,1-dioxo-1H-1λ⁶-benzo[d]isothiazol-3-ylamino)-ethanol 
• 875305-43-4 [rac]-(4-tert-butyl-benzyl)-[2-(3,4-dichloro-phenyl)-2-hydroxy-ethyl]-amine 
• 1254941-84-8 2-(3-([1,2,4]triazolo[1,5-a;]pyridin-6-yl)benzylamino)-1-(3,4-dichlorophenyl)ethanol 
• 1254942-00-1 5-([1,2,4]triazolo[1,5-α]pyridin-6-yl)-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydroisoquinoline 
• 1254941-99-5 7-([1,2,4]triazolo[1,5-a]pyridin-6-yl)-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydroisoquinoline 

Relevant articles and documents

ARYL, HETEROARYL, AND HETEROCYCLE SUBSTITUTED TETRAHYDROISOQUINOLINES AND USE THEREOF

Novel aryl, heteroaryl, and non-aromatic heterocyle substituted tetrahydroisoquinolines are described in the present invention. These compounds are used in the treatment of various neurological and physiological disorders. Methods of making these compounds are also described in the present invention.

Novel 1H-(benzimidazol-2-yl)-1H-pyridin-2-one inhibitors of insulin-like growth factor I (IGF-1R) kinase

A novel class of 1H-(benzimidazol-2-yl)-1H-pyridin-2-one inhibitors of insulin-like growth factor I (IGF-1R) kinase is described. This report discusses the SAR of 4-(2-hydroxy-2-phenylethylamino)-substituted pyridones with improved IGF-1R potency.

On the synthesis of β receptor blockers

-