5440-27-7

Basic information

• Product Name: 3-AMINO-4-PHENYLBUTAN-2-ONE HYDROCHLORIDE
• Synonyms: 3-AMINO-4-PHENYLBUTAN-2-ONE HYDROCHLORIDE
• CAS NO: 5440-27-7
• Molecular Formula: C₁₀H₁₃NO*ClH
• Molecular Weight: 199.68
• Mol File: 5440-27-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 261.6°Cat760mmHg
• Flash Point: 112°C
• Appearance: /
• Density: 1.043g/cm³
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 3-AMINO-4-PHENYLBUTAN-2-ONE HYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-AMINO-4-PHENYLBUTAN-2-ONE HYDROCHLORIDE(5440-27-7)
• EPA Substance Registry System: 3-AMINO-4-PHENYLBUTAN-2-ONE HYDROCHLORIDE(5440-27-7)

Safety Data

• Hazardous Substances Data: 5440-27-7(Hazardous Substances Data)

Usage

Description

3-AMINO-4-PHENYLBUTAN-2-ONE HYDROCHLORIDE is a hydrochloride derivative of 3-amino-4-phenylbutan-2-one, a ketone compound used in the pharmaceutical and research industries. It serves as a building block or intermediate in the synthesis of various drugs and organic compounds and has potential pharmacological effects, particularly in the treatment of neurological and psychiatric disorders.
Used in Pharmaceutical Industry:
3-AMINO-4-PHENYLBUTAN-2-ONE HYDROCHLORIDE is used as a building block for the synthesis of various drugs and organic compounds, contributing to the development of new therapeutics and biologically active compounds.
Used in Research Industry:
3-AMINO-4-PHENYLBUTAN-2-ONE HYDROCHLORIDE is used as an intermediate in organic synthesis, facilitating the creation of complex molecules for research purposes.
Used in Drug Discovery and Development:
3-AMINO-4-PHENYLBUTAN-2-ONE HYDROCHLORIDE is used as a key component in the discovery and development of new drugs, particularly those targeting neurological and psychiatric disorders, due to its potential pharmacological effects.

Upstream product

• 5440-25-5 3-(hydroxyimino)-4-phenylbutan-2-one 
• 5463-26-3 3-acetylamino-4-phenyl-2-butanone 
• 55902-35-7 Z α-nitrobenzylidene acetone 

Downstream Products

• 78631-22-8 dibenzyl-2,5 dimethyl-3,6 pyrazine 
• 1456782-12-9 3-benzyl-N-(tert-butyl)-2-methyl-4-(4-methylbenzoyl)-4,5-dihydro-3H-1,4-benzodiazepine-5-carboxamide 
• 1456782-11-8 3-benzyl-N-(tert-butyl)-4-(4-chlorobenzoyl)-2-methyl-4,5-dihydro-3H-1,4-benzodiazepine-5-carboxamide 
• 120881-36-9 (1S,5R,7S)-3-(1-Benzyl-2-oxo-propyl)-1,5,7-trimethyl-2,4-dioxo-3-aza-bicyclo[3.3.1]nonane-7-carboxylic acid methyl ester 
• 120881-34-7 (1S,5R,7S)-3-(1-Benzyl-2-oxo-propyl)-1,5,7-trimethyl-2,4-dioxo-3-aza-bicyclo[3.3.1]nonane-7-carboxylic acid 
• 117535-97-4 4-(3-chloropropoxy)-N-<3-(4-phenyl-2-oxobutyl)>phenylacetamide 
• 120881-32-5 (1R,5S,7R)-1,5,7-Trimethyl-2,4-dioxo-3-oxa-bicyclo[3.3.1]nonane-7-carboxylic acid (1-benzyl-2-oxo-propyl)-amide 

Relevant articles and documents

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The object of the present invention is to provide a new thiazolidinedione derivative exhibiting excellent hypoglycemic and hypolipidemic action. Thiazolidinedione derivative represented by the general formula: STR1 wherein n represents an integer from 1 t

Preparation, reduction chimique et electrochimique d'α-nitrostyrylcetones - synthese d'heterocycles azotes

Nitration of styryl ketones with nitrogen peroxide leads to the corresponding α-nitroethylenic ketones in good yield.However, the presence of methoxy groups involves a nitration on the aromatic nucleus.LiAlH4 reduction of α-nitrostyrylketones yields the c