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2-[(2-HYDROXY-ETHYL)-METHYL-AMINO]-1-PHENYL-ETHANOL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23175-16-8

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23175-16-8 Usage

Type of compound

Alcohol derivative

Functional groups

Phenyl group, hydroxyl group, amino group

Usage

Reagent in organic synthesis and pharmaceutical research

Potential applications

Drug and medicinal compound development

Additional uses

Industrial processes and materials science

Check Digit Verification of cas no

The CAS Registry Mumber 23175-16-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,1,7 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 23175-16:
(7*2)+(6*3)+(5*1)+(4*7)+(3*5)+(2*1)+(1*6)=88
88 % 10 = 8
So 23175-16-8 is a valid CAS Registry Number.

23175-16-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-hydroxyethyl(methyl)amino]-1-phenylethanol

1.2 Other means of identification

Product number -
Other names HMS1718O03

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:23175-16-8 SDS

23175-16-8Relevant academic research and scientific papers

SUBSTITUTED PIPERAZINES AS CB1 ANTAGONISTS

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Page/Page column 164; 164-165, (2009/03/07)

Compounds of Formula (I) or pharmaceutically acceptable salts, solvates, or esters thereof, are useful in treating diseases or conditions mediated by CB1 receptors, such as metabolic syndrome and obesity, neuroinflammatory disorders, cognitive disorders and psychosis, addiction (e.g., smoking cessation), gastrointestinal disorders, and cardiovascular conditions.

Synthesis and pharmacological testing of 1,2,3,4,10,14b-hexahydro-6-methoxy-2-methyldibenzo[c,f]pyrazino[1,2-a]azepin and its enantiomers in comparison with the two antidepressants mianserin and mirtazapine

Wikstr?m, H?kan V.,Mensonides-Harsema, Marguérite M.,Cremers, Thomas I. F. H.,Moltzen, Ejner K.,Arnt, J?rn

, p. 3280 - 3285 (2007/10/03)

The synthesis and resolution of 1,2,3,4,10,14b-hexahydro-6-methoxy-2-methy[dibenzo[c,f]pyrazino [1,2-α]azepin (6-methoxymianserin, 6) are described. Furthermore, the in vitro and in vivo effects of 6 and its enantiomers are presented. 6 displayed high aff

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