103565-48-6

Basic information

• Product Name: 2-AMINO-1-(2,5-DIMETHOXYPHENYL)-1-PROPANONE
• Synonyms: 2-AMINO-1-(2,5-DIMETHOXYPHENYL)-1-PROPANONE;1-(2,5-Dimethoxybenzoyl)ethanamine
• CAS NO: 103565-48-6
• Molecular Formula: C₁₁H₁₅NO₃*ClH
• Molecular Weight: 209.2417
• Mol File: 103565-48-6.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-AMINO-1-(2,5-DIMETHOXYPHENYL)-1-PROPANONE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-AMINO-1-(2,5-DIMETHOXYPHENYL)-1-PROPANONE(103565-48-6)
• EPA Substance Registry System: 2-AMINO-1-(2,5-DIMETHOXYPHENYL)-1-PROPANONE(103565-48-6)

Safety Data

• Hazardous Substances Data: 103565-48-6(Hazardous Substances Data)

Usage

General Description

2-AMINO-1-(2,5-DIMETHOXYPHENYL)-1-PROPANONE is a chemical compound that contains an amino group and a propanone group. It also has a 2,5-dimethoxyphenyl group attached to the amino group. 2-AMINO-1-(2,5-DIMETHOXYPHENYL)-1-PROPANONE is commonly used in organic synthesis and pharmaceutical research as a building block for the development of various drugs and pharmaceuticals. It can also be used as a reagent in chemical reactions to form new compounds with different properties and applications. The specific structure and properties of this compound make it valuable in a wide range of chemical and pharmaceutical applications.

Upstream product

• 121347-31-7 1-(2,5-dimethoxyphenyl)-2-hydroxyimino-1-acetone 
• 5803-30-5 2',5'-dimethoxypropiophenone 
• 742095-47-2 (RS)-2-trifluoroacetamido-1-(2,5-dimethoxyphenyl)-1-propanone 

Downstream Products

• 390-28-3 2-amino-1-(2,5-dimethoxyphenyl)-1-propanol 

Relevant articles and documents

A salt structure the armor oxygen is bright erythro method for the preparation of acid

A disclosed preparation method for erythro-structure methoxamine hydrochloride comprises the following steps: (1) dissolving an initial raw material 2,5-dimethylpropiophenone in an organic solvent, under the condition of introducing dry hydrogen chloride gas, dropwise adding a 1-butyl nitrite solution to perform an oximation reaction, so as to obtain an intermediate I; (2) under the acidic condition, taking a methanol solution as a solvent, take palladium on activated carbon as a catalyst, employing hydrogen to reduce the oximido group in the intermediate I, so as to obtain an intermediate II; and (3) performing hydrogenation reduction reaction on the intermediate II to obtain the erythro-structure methoxamine hydrochloride. The method provided by the invention is simple in operation, economic, environment-friendly, mild in reaction conditions, excellent in product quality and high in yield, and can help to obtain the single erythro-structure methoxamine hydrochloride.