6924-15-8

Basic information

• Product Name: 2-AMINO-1-(3,4-DIMETHOXY-PHENYL)-ETHANOL
• Synonyms: 2-AMINO-1-(3,4-DIMETHOXY-PHENYL)-ETHANOL;AKOS BBV-002394;OTAVA-BB 1055879
• CAS NO: 6924-15-8
• Molecular Formula: C₁₀H₁₅NO₃
• Molecular Weight: 197.23
• Product Categories: pharmacetical
• Mol File: 6924-15-8.mol
• Article Data: 13

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-AMINO-1-(3,4-DIMETHOXY-PHENYL)-ETHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2-AMINO-1-(3,4-DIMETHOXY-PHENYL)-ETHANOL(6924-15-8)
• EPA Substance Registry System: 2-AMINO-1-(3,4-DIMETHOXY-PHENYL)-ETHANOL(6924-15-8)

Safety Data

• Hazardous Substances Data: 6924-15-8(Hazardous Substances Data)

Usage

General Description

2-AMINO-1-(3,4-DIMETHOXY-PHENYL)-ETHANOL, also known as 4-Methylpropiophenone, is a chemical compound with the formula C11H15NO3. It is classified as an amino alcohol and contains a phenyl ring with two methoxy groups attached, as well as an amino group and a hydroxyl group. 2-AMINO-1-(3,4-DIMETHOXY-PHENYL)-ETHANOL has been studied for its potential pharmaceutical properties, including its potential as a psychoactive agent. It may also have applications in the field of organic synthesis and as a building block for the production of other chemical compounds. Additional research is needed to further understand its potential uses and applications.

Upstream product

• 52196-76-6 2-diazo-1-(3,4-dimethoxyphenyl)ethan-1-one 
• 65961-86-6 (3,4-dimethoxy-phenyl)-glyoxylonitrile 
• 99076-44-5 (+/-)-3,4-Dimethoxy-mandelsaeure-amid 
• 75-52-5 nitromethane 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 6309-18-8 2-(3,4-dimethoxyphenyl)-2-hydroxyacetonitrile 
• 95392-01-1 2-(3,4-dimethoxyphenyl)-2-((trimethylsilyl)oxy)acetonitrile 
• 64-19-7 acetic acid 
• 64-17-5 ethanol 
• 46729-91-3 1-(3,4-dimethoxyphenyl)-2-nitroethan-1-one 
• 68413-92-3 sodium (3,4-dimethoxyphenyl)(hydroxy)methanesulfonate 
• 39220-86-5 2-nitro-1-(3,4-dimethoxyphenyl)ethanol 
• 1131-62-0 1-(3,4-dimethoxyphenyl)ethanone 
• 1835-02-5 2-Bromo-1-(3,4-dimethoxyphenyl)ethanone 

Downstream Products

• 54837-88-6 piperonal-(β-hydroxy-3,4-dimethoxy-phenethylimine) 
• 78004-24-7 (3,4-dimethoxy-phenyl)-acetic acid-(β-hydroxy-3,4-dimethoxy-phenethylamide) 
• 109158-18-1 5-(3,4-dimethoxy-phenyl)-2-styryl-oxazolidine 
• 3865-99-4 5-(3,4-dimethoxy-phenyl)-4,5-dihydro-oxazol-2-ylamine 
• 743358-61-4 2-(4-Chloro-benzylamino)-1-(3,4-dimethoxy-phenyl)-ethanol 
• 83633-37-8 N-<2-hydroxy-2-(3,4-dimethoxyphenyl)ethyl>-4-nitrobenzeneacetamide 
• 54837-87-5 [2-(3,4-Dimethoxy-phenyl)-2-hydroxy-ethyl]-carbamic acid ethyl ester 
• 25932-34-7 6,7-dimethoxy-1-(4-nitrobenzyl)isoquinoline 
• 83633-13-0 4-[(6,7-dimethoxy-1-isoquinolinyl)methyl]benzenamine 
• 83633-23-2 N-(2-chloroethyl)-4-[(6,7-dimethoxy-1-isoquinolinyl)methyl]benzenamine 
• 83633-15-2 N-{4-[(6,7-dimethoxy-1-isoquinolinyl)methyl]phenyl}propenamide 
• 83633-40-3 N-<4-<(6,7-dimethoxy-1-isoquinolinyl)methyl>phenyl>-2,2'-aminobis 
• 83633-34-5 N,N-bis(2-chloroethyl)-4-[(6,7-dimethoxy-1-isoquinolinyl)methyl]benzenamine 
• 83633-19-6 2-chloro-N-{4-[(6,7-dimethoxy-1-isoquinolinyl)methyl]phenyl}acetamide 

Relevant articles and documents

Chiral-Organotin-Catalyzed Kinetic Resolution of Vicinal Amino Alcohols

A highly efficient kinetic resolution of racemic amino alcohols has been achieved for the first time with a chiral tin catalyst. A chiral organotin compound with 3,4,5-trifluorophenyl groups at the 3,3′-positions of the binaphthyl framework enabled this transformation with excellent yield and high enantioselectivity. The process tolerates aryl- and alkyl-substituted amino alcohols and a variety of other substrates, affording the corresponding products in high enantioselectivity and with s factors up to >500.

SUBSTITUTED 8 - AMINO - IMIDAZO [1, 2-A] PYRAZ1NES AS ANTIBACTERIAL AGENTS

The present invention relates to substituted imidazo[1,2-a]pyrazines of Formula (I) and their use as antibacterial agents.

First total synthesis of crispine B by nitro aldol and the Bischler-Napieralski reaction

A pyrrolo[2,1-a]isoquinoline alkaloid, crispine B, was firstly synthesized in 55% overall yield from 3,4-dimethoxyaldehyde via five steps by employing nitro-aldol reaction and the Bischler-Napieralski reaction.