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alpha-(aminomethyl)-3,4-dichlorobenzyl alcohol is a chemical compound characterized by the molecular formula C9H10Cl2NO and a molecular weight of 225.09 g/mol. It is a derivative of 3,4-dichlorobenzyl alcohol, featuring an aminomethyl group attached to the alpha carbon. alpha-(aminomethyl)-3,4-dichlorobenzyl alcohol is recognized for its potent antimicrobial properties, which have led to its widespread use in various applications.

3567-82-6

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3567-82-6 Usage

Uses

Used in Pharmaceutical Industry:
alpha-(aminomethyl)-3,4-dichlorobenzyl alcohol is used as an antifungal and antibacterial agent for its effective antimicrobial properties, playing a crucial role in the treatment and prevention of various infections and diseases.
Used in Personal Care Products:
In the personal care industry, alpha-(aminomethyl)-3,4-dichlorobenzyl alcohol is used as an active ingredient in mouthwashes, skin cleansers, and topical antiseptics, where it helps maintain hygiene and prevent microbial growth.
Used in Research and Development:
alpha-(aminomethyl)-3,4-dichlorobenzyl alcohol is also utilized in research for its potential as a therapeutic agent, with ongoing studies exploring its efficacy in treating a broader range of infections and diseases, thereby expanding its applications in the medical field.

Check Digit Verification of cas no

The CAS Registry Mumber 3567-82-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,6 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3567-82:
(6*3)+(5*5)+(4*6)+(3*7)+(2*8)+(1*2)=106
106 % 10 = 6
So 3567-82-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H9Cl2NO/c9-6-2-1-5(3-7(6)10)8(12)4-11/h1-3,8,12H,4,11H2

3567-82-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-1-(3,4-dichlorophenyl)ethanol

1.2 Other means of identification

Product number -
Other names EINECS 222-659-5

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3567-82-6 SDS

3567-82-6Relevant academic research and scientific papers

ARYL, HETEROARYL, AND HETEROCYCLE SUBSTITUTED TETRAHYDROISOQUINOLINES AND USE THEREOF

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, (2010/12/17)

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.

ARYL-HYDROXYETHYLAMINO-PYRIMIDINES AND TRIAZINES AS MODULATORS OF FATTY ACID AMIDE HYDROLASE

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Page/Page column 41-42, (2009/10/18)

Certain aryl-hydroxyethylamino-pyrimidine and triazine compounds are described, which are useful as FAAH inhibitors. Such compounds may be used in pharmaceutical compositions and methods for the treatment of disease states, disorders, and conditions mediated by fatty acid amide hydrolase (FAAH) activity, such as anxiety, pain, inflammation, sleep disorders, eating disorders, energy metabolism disorders, and movement disorders (e.g., multiple sclerosis). Methods of synthesizing such compounds are also disclosed.

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

Wittman, Mark D.,Balasubramanian, Balu,Stoffan, Karen,Velaparthi, Upender,Liu, Pieying,Krishnanathan, Subramaniam,Carboni, Joan,Li, Aixin,Greer, Ann,Attar, Ricardo,Gottardis, Marco,Chang, Chiehying,Jacobson, Bruce,Sun, Yax,Hansel, Steven,Zoeckler, Mary,Vyas, Dolatrai M.

, p. 974 - 977 (2007/10/03)

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.

Indole, indazole and indoline derivatives as CETP inhibitors

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Page/Page column 29, (2010/02/15)

The present invention relates to compounds of formula (I): wherein —X—Y—, R1 to R11 and n are as defined in the description and claims, and pharmaceutically acceptable salts thereof. The compounds are useful for the treatment and/or prevention of diseases which are mediated by CETP inhibitors.

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