148223-47-6

Basic information

• Product Name: 2-(3-BENZYLOXY-4-METHOXY-PHENYL)-ETHYLAMINE HCL
• Synonyms: 2-(3-BENZYLOXY-4-METHOXY-PHENYL)-ETHYLAMINE HCL;2-(3-Benzyloxy-4-methoxy-phenyl)-ethylamine;2-(3-Benzyloxy-4-methoxyphenyl)ethylaminehydrochloride;2-(3-(benzyloxy)-4-methoxyphenyl)ethanamine hydrochloride
• CAS NO: 148223-47-6
• Molecular Formula: C₁₆H₁₉NO₂*ClH
• Molecular Weight: 0
• Mol File: 148223-47-6.mol
• Article Data: 1

Chemical Properties

• Melting Point: 166 °C
• Appearance: /
• CAS DataBase Reference: 2-(3-BENZYLOXY-4-METHOXY-PHENYL)-ETHYLAMINE HCL(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3-BENZYLOXY-4-METHOXY-PHENYL)-ETHYLAMINE HCL(148223-47-6)
• EPA Substance Registry System: 2-(3-BENZYLOXY-4-METHOXY-PHENYL)-ETHYLAMINE HCL(148223-47-6)

Safety Data

• Hazardous Substances Data: 148223-47-6(Hazardous Substances Data)

Usage

General Description

2-(3-Benzyloxy-4-methoxy-phenyl)-ethylamine HCL is a chemical compound with the molecular formula C17H21NO2·HCl. It is a derivative of phenethylamine and is commonly used in organic synthesis. 2-(3-BENZYLOXY-4-METHOXY-PHENYL)-ETHYLAMINE HCL is often utilized as a reagent in the production of various pharmaceuticals and other organic compounds. It is a white to off-white crystalline solid at room temperature and is soluble in water. 2-(3-Benzyloxy-4-methoxy-phenyl)-ethylamine HCL has applications in the development of new medications and in the production of fine chemicals.

InChI:InChI=1/C16H19NO2.ClH/c1-18-15-8-7-13(9-10-17)11-16(15)19-12-14-5-3-2-4-6-14;/h2-8,11H,9-10,12,17H2,1H3;1H

Upstream product

• 63909-29-5 3-benzyloxy-4-methoxy-β-nitrostyrene 

Downstream Products

• 1233354-87-4 C₃₃H₃₄FNO₈S 

Relevant articles and documents

Synthesizing method of 6-benzyloxy-7-methoxy-3,4-dihydroisoquinoline

The invention discloses a synthesizing method of 6-benzyloxy-7-methoxy-3,4-dihydroisoquinoline in the field of medicine synthesizing. The synthesizing method includes: dissolving 3-benzyloxy-4- methoxy phenylethylamine or hydrochloride thereof in the mixed liquid of glacial acetic acid and trifluoroacetic acid to generate the 6-benzyloxy-7-methoxy-3,4-dihydroisoquinoline under the effect of hexamethylene tetramine in a closed-loop manner. The synthesizing method has the advantages that the 3-benzyloxy-4- methoxy phenylethylamine is subjected to one-step closed-loop reaction under the effect ofhexamethylene tetramine to prepare the target product, and the synthesizing route is short; the 3-benzyloxy-4- methoxy phenylethylamine and the 6-benzyloxy-7-methoxy-3,4-dihydroisoquinoline are purified in a recrystallization manner to prepare the hydrochloride of the 3-benzyloxy-4- methoxy phenylethylamine and the 6-benzyloxy-7-methoxy-3,4-dihydroisoquinoline, the purification operation is simple, and the obtained compound is stable in property and can be conveniently stored for a long time.