17959-64-7

Basic information

• Product Name: 2-PHENOXYETHYLAMINEHCL
• Synonyms: 2-PHENOXYETHYLAMINEHCL;(2-Phenoxyethyl)amine hydrochloride
• CAS NO: 17959-64-7
• Molecular Formula: C₈H₁₁NO*ClH
• Molecular Weight: 173.64
• Mol File: 17959-64-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 230.3 °C at 760 mmHg
• Flash Point: 97.9 °C
• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 2-PHENOXYETHYLAMINEHCL(CAS DataBase Reference)
• NIST Chemistry Reference: 2-PHENOXYETHYLAMINEHCL(17959-64-7)
• EPA Substance Registry System: 2-PHENOXYETHYLAMINEHCL(17959-64-7)

Safety Data

• Hazardous Substances Data: 17959-64-7(Hazardous Substances Data)

Usage

General Description

2-Phenoxyethylamine hydrochloride (2-PEA HCl) is a chemical compound that is widely used in the pharmaceutical and chemical industries. It is a derivative of phenethylamine and is commonly used as a precursor in the synthesis of various drugs and other organic compounds. 2-PEA HCl has also been studied for its potential therapeutic applications, including its ability to act as a vasodilator and its potential use in the treatment of neurological disorders. 2-PHENOXYETHYLAMINEHCL is known for its mild odor and is typically sold as a white or off-white crystalline powder.

Upstream product

• 108-95-2 phenol 
• 1758-46-9 2-phenoxyethanamine 
• 921596-28-3 tert-butyl (2-phenoxyethyl)carbamate 

Downstream Products

• 64463-90-7 1-(2-Bromo-phenoxy)-3-(2-phenoxy-ethylamino)-propan-2-ol 
• 1205561-38-1 2-iodo-4-methyl-N-(2-phenoxyethyl)-1,3-thiazole-5-carboxamide 
• 1353573-75-7 5-{[(2-phenoxyethyl)amino]methyl}-2,2-diphenylcyclopentan-1-one 
• 155768-97-1 2-chloro-N-(2-phenoxyethyl)adenosine 
• 64463-54-3 1-Phenoxy-3-(2-phenoxy-ethylamino)-propan-2-ol 
• 64596-96-9 1-(4-Benzyloxy-phenoxy)-3-(2-phenoxy-ethylamino)-propan-2-ol 
• 64463-83-8 1-(2-Phenoxy-ethylamino)-3-p-tolyloxy-propan-2-ol 
• 40077-26-7 2-[(2-Phenoxy-ethylamino)-methyl]-3,4-dihydro-2H-naphthalen-1-one 
• 22303-44-2 5-amino-3-(2-phenoxy-ethyl)-[1,2,3]oxadiazolium betaine 

Relevant articles and documents

Double - (to - alkoxybenzyl propenone) glutathione - S - transfers the sulfur of the enzyme dives inhibitors

The invention discloses a bis-(p-alkoxy benzene acrylketone) like glutathione-S-transferase potential inhibitor. Structure and living features of the potential inhibitor are as follows: two p-alkoxy benzene acrylketone units are linked to two amino groups, alcoholic hydroxyl groups and carboxyl groups or one amino group and one alcoholic hydroxyl group which are spaced by less than 8 single bonds through amide and/or ester bond, wherein compounds obtained are substrate and inhibitor of glutathione-S-transferase, namely GST; the GST catalyzes carbon-carbon bond and reduced glutathione, namely GSH, of alpha, beta-unsaturated ketone of each p-alkoxy benzene acrylketone unit in the compounds and generates a compound, namely product, through Michael addition. The product shows a stronger inhibiting efficacy on the GST, so that the compound is a GST potential inhibitor; the product has a stronger inhibiting efficacy on human GST isozyme mu in comparison with human GST isozyme alpha and pi; and the compounds can enter into cells, and can enhance inhibiting effect of cis-platinum on drug-resistant carcinoma cell growth.

THIAZOLE DERIVATIVES AS STEAROYL COA DESATURASE INHIBITORS

The present invention provides thiazole derivatives as Stearoyl CoA Desaturase (SCD) inhibitors. In particular, the compounds described herein are useful for treating or preventing diseases, conditions and/or disorders modulated by Stearoyl CoA Desaturase