6956-60-1

Basic information

• Product Name: 2-(butylsulfanyl)quinazolin-4(1H)-one
• Synonyms: 2-(Butylsulfanyl)quinazolin-4(1H)-one; 2-(Butylsulfanyl)quinazolin-4(3H)-one; 4(1H)-quinazolinone, 2-(butylthio)-; 4(3H)-Quinazolinone, 2-(butylthio)-
• CAS NO: 6956-60-1
• Molecular Formula: C₁₂H₁₄N₂OS
• Molecular Weight: 234.3174
• Mol File: 6956-60-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 387.2°C at 760 mmHg
• Flash Point: 188°C
• Density: 1.23g/cm³
• Vapor Pressure: 3.36E-06mmHg at 25°C
• Refractive Index: 1.63
• CAS DataBase Reference: 2-(butylsulfanyl)quinazolin-4(1H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(butylsulfanyl)quinazolin-4(1H)-one(6956-60-1)
• EPA Substance Registry System: 2-(butylsulfanyl)quinazolin-4(1H)-one(6956-60-1)

Safety Data

• Hazardous Substances Data: 6956-60-1(Hazardous Substances Data)

Usage

Compound type

Quinazolinone derivative

Attached groups

Sulfur atom and a butyl group

Potential pharmacological properties

Yes

Potential applications

Medicinal chemistry, drug discovery and development, new therapeutics for various medical conditions

Precise pharmacological and biological activities

Under investigation

Promise as a potential lead compound

Yes

Upstream product

• 103748-72-7 2-{[(Toluene-4-sulfonyl)-(triphenyl-λ⁵-phosphanylidene)-methyl]-azo}-benzaldehyde 
• 109-79-5 n-butanethiol 
• 103748-77-2 2-p.tosyl-4-oxo-dihydroquinazoline 
• 118-92-3 anthranilic acid 
• 109-65-9 1-bromo-butane 
• 13906-09-7 2-mercapto-3H-quinazolin-4-one 
• 13906-09-7 2-thioxo-2,3-dihydro-1H-quinazolin-4-one 
• 109-69-3 n-Butyl chloride 

Relevant articles and documents

SYNTHESIS OF 2-ALKYLTHIOQUINAZOL-4-ONES

Alkylation of 2-thioxoquinazol-4-one by different alkylating agents was studied, and it was found that the reaction proceeds at the exocyclic sulfur atom with the formation of 2-alkylthioquinazol-4-ones.

SYNTHESIS AND ALKYLATION OF 2-MERCAPTO-4-QUINAZOLONE AND THE FUNGICIDAL ACTIVITIES OF THE COMPOUNDS OBTAINED

A convenient method of obtaining 2-mercapto-4-quinazolone has been developed and the alkylation of its ambidentate anions has been studied.It has been found that they exhibit a dual reactivity in alkylation reactions.It has been shown that alkylated 2-mercapto-4-quinazolones possess a moderate fungicidal activity.