2982-54-9

Basic information

• Product Name: 4-BENZYLOXY-3-AMINO-A-[-BENZYL-N-(1-METHYL-2P-METHOXY PHENYL ETHER) AMINO-METHYL BENZYL ALCOHOL
• Synonyms: 4-BENZYLOXY-3-AMINO-A-[-BENZYL-N-(1-METHYL-2P-METHOXY PHENYL ETHER) AMINO-METHYL BENZYL ALCOHOL;4-BENZYLOXY-PHENETHYLAMINE HCL;4-Benzyloxy-phenethylamine hydrochloride;2-(4-Benzyloxy-phenyl)-ethylamine hydrochloride;2-(4-benzoxyphenyl)ethylamine hydrochloride;2-(4-phenylmethoxyphenyl)ethanamine hydrochloride;2-(4-Benzyloxy-phenyl)-ethylamine, HCl;2-(4-(Benzyloxy)phenyl)ethanamine hydrochloride
• CAS NO: 2982-54-9
• Molecular Formula: C₁₅H₁₇NO*ClH
• Molecular Weight: 263.77
• Mol File: 2982-54-9.mol
• Article Data: 8

Chemical Properties

• Melting Point: 196-206 °C (decomp)
• Boiling Point: 370.5°C at 760 mmHg
• Flash Point: 179.6°C
• Appearance: /
• Vapor Pressure: 1.1E-05mmHg at 25°C
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: 4-BENZYLOXY-3-AMINO-A-[-BENZYL-N-(1-METHYL-2P-METHOXY PHENYL ETHER) AMINO-METHYL BENZYL ALCOHOL(CAS DataBase Reference)
• NIST Chemistry Reference: 4-BENZYLOXY-3-AMINO-A-[-BENZYL-N-(1-METHYL-2P-METHOXY PHENYL ETHER) AMINO-METHYL BENZYL ALCOHOL(2982-54-9)
• EPA Substance Registry System: 4-BENZYLOXY-3-AMINO-A-[-BENZYL-N-(1-METHYL-2P-METHOXY PHENYL ETHER) AMINO-METHYL BENZYL ALCOHOL(2982-54-9)

Safety Data

• Hazardous Substances Data: 2982-54-9(Hazardous Substances Data)

Usage

General Description

4-BENZYLOXY-3-AMINO-A-[-BENZYL-N-(1-METHYL-2P-METHOXY PHENYL ETHER) AMINO-METHYL BENZYL ALCOHOL is a complex chemical compound with various substituents and functional groups. It contains a benzyl group, an amino group, and a phenyl ether group, as well as a methyl and methoxy group. The compound also contains an alcohol functional group and multiple benzyl groups. This chemical is likely to have a wide range of uses, including potentially as a pharmaceutical intermediate or in the synthesis of other organic compounds. The specific properties and uses of this chemical would need to be further investigated and determined based on its specific structure and characteristics.

InChI:InChI=1/C15H17NO.ClH/c16-11-10-13-6-8-15(9-7-13)17-12-14-4-2-1-3-5-14;/h1-9H,10-12,16H2;1H

Upstream product

• 74447-33-9 1-(2'-azidoethyl)-4-(benzyloxy)benzene 
• 100-39-0 benzyl bromide 
• 838-96-0 2-[4-(benzyloxy)phenyl]acetonitrile 
• 14191-95-8 4-cyanomethylphenol 
• 51-67-2 tyrosamine 
• 74447-34-0 1-azido-2-(4-hydroxyphenyl)ethane 
• 64318-28-1 N-t-butoxycarbonyl-tyramine 
• 182921-01-3 N-(tert-butoxycarbonyl)-2-[4-(benzyloxy)phenyl]ethylamine 
• 74447-35-1 1-azido-2-(4-methylsulphonyloxyphenyl)ethane 

Downstream Products

• 60-19-5 tyramine hydrochloride 
• 1415684-17-1 (2S,3R,3aS,12bR)-1,2,3,3a,4,5,7,8-octahydro-11-benzyloxy-2-methyl-5-oxo-cyclopenta[2,3]pyrrolo[2,1-a]isoquinoline-3-carboxylic acid 
• 1415684-16-0 (2S,3R,3aS,12bR)-1,2,3,3a,4,5,7,8-octahydro-11-benzyloxy-2-methyl-3-nitromethyl-5-oxo-cyclopenta[2,3]pyrrolo[2,1-a]isoquinoline 
• 51179-05-6 2-(4-(benzyloxy)phenyl)ethanamine 
• 1410800-32-6 N-(4-(benzyloxy)phenethyl)-1H-pyrrolo[3,2-c]pyridine-2-carboxamide 
• 920525-70-8 3-((2-(4-benzyloxyphenyl)-ethylamino)-methyl)-7-methyl-chromen-2-one 
• 74447-32-8 O,O-dibenzoyltyrosol 
• 501-94-0 p-hydroxyphenethyl alcohol 

Relevant articles and documents

TETRAHYDROPROTOBERBERINE COMPOUND, PREPARATION METHOD THEREFOR AND USES THEREOF, AND PHARMACEUTICAL COMPOSITION

The present invention provides a tetrahydroprotoberberine compound represented by the formula (I), enantiomers, diastereomers, racemates and mixtures thereof, and pharmaceutically acceptable salts, crystalline hydrates and solvates thereof. The invention also provides a method for preparing the compound and the use thereof in the preparation of a medicament for preventing and/or treating central nervous system diseases.

Diverse alkaloid-like structures from a common building block

A wealth of unique enantiopure polycyclic alkaloid-like scaffolds can be prepared on a multigram scale in only a few steps from a common, commercially available intermediate. The attached nitromethyl group can then be used to construct highly diverse func

NOVEL CHROMEN-2-ONE BASED HYDROXAMIC ACID DERIVATIVES HAVING ANTI-INFLAMMATORY ACTIVITY, THE PREPARATION THEREOF AND A COMPOSITION CONTAINING THE SAME FOR TREATING INFLAMMATORY DISEASE

The present invention relates to novel chromen-2-one based hydroxamic acid derivatives having anti-inflammatory activity, the preparation thereof and a composition containing the same for treating inflammatory disease.