2400-96-6

Basic information

• Product Name: 2,4(1H,3H)-Quinazolinedione, 3-(4-bromophenyl)-
• CAS NO: 2400-96-6
• Molecular Formula: C14H9BrN2O2
• Molecular Weight: 317.142
• Mol File: 2400-96-6.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: 2,4(1H,3H)-Quinazolinedione, 3-(4-bromophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4(1H,3H)-Quinazolinedione, 3-(4-bromophenyl)-(2400-96-6)
• EPA Substance Registry System: 2,4(1H,3H)-Quinazolinedione, 3-(4-bromophenyl)-(2400-96-6)

Safety Data

• Hazardous Substances Data: 2400-96-6(Hazardous Substances Data)

Usage

Molecular Weight

255.04 g/mol

Structure

Heterocyclic compound with a quinazoline ring structure and a bromophenyl group attached

Appearance

Not provided in the material

Solubility

Not provided in the material

Melting Point

Not provided in the material

Boiling Point

Not provided in the material

Spectra

Not provided in the material

Biological Activity

Potential applications in medicinal chemistry as it may possess biological activities

Use

Could be used as a building block in organic synthesis and pharmaceutical drug development

Value

Its physical and chemical properties make it a valuable molecule for further research and potential applications.

Upstream product

• 19062-36-3 2-hydrazino-3-(4-bromophenyl)quinazoline-4-(3H)-one 
• 106-40-1 4-bromo-aniline 
• 2493-02-9 4-bromophenyl isocyanate 
• 1567-02-8 C₁₅H₁₃BrN₂O₃ 
• 91-56-5 indole-2,3-dione 
• 133764-46-2 [3-(4-Bromo-phenyl)-4-oxo-3,4-dihydro-quinazolin-2-ylsulfanyl]-acetic acid hydrazide 
• 1028-39-3 3-(4-bromophenyl)-2-thioxo-2,3-dihydroquinazoline-4(1H)-one 
• 50735-55-2 2-amino-N-(4-bromophenyl)benzamide 
• 118-48-9 isatoic anhydride 
• 32315-10-9 bis(trichloromethyl) carbonate 
• 2385-26-4 N-(4-bromophenyl)-2-nitrobenzamide 
• 57-13-6 urea 
• 33829-00-4 3-[(4-bromophenyl)imino]-1,3-dihydro-2H-indol-2-one 
• 201230-82-2 carbon monoxide 

Relevant articles and documents

2-[3-(4-morpholinyl)propylamine]-3-aryl-4-quinolinone compounds and application thereof

The invention belongs to the technical field of medicines and relates to 2-[3-(4-morpholinyl)propylamine]-3-aryl-4-quinolinone compounds and an application thereof. 2-[3-(4-morpholinyl)propylamine]-3-aryl-4-quinolinone derivatives comprise stereisomers and pharmaceutically applicable salts of the compounds and have the general structural formula shown in the description, wherein R is described inthe claims and description. The 2-[3-(4-morpholinyl)propylamine]-3-aryl-4-quinolinone derivatives and pharmaceutically applicable acid-added salts of the compounds can be combined with existing medicines or used separately to serve as influenza virus inhibitors to treat influenza and have better curative effects on various type-A influenza in particular.

Synthesis, molecular structure and spectroscopic studies of some new quinazolin-4(3H)-one derivatives; An account on the N- versus S-Alkylation

A new series of N- and S-alkylated products of 3-aryl-1H,3H-quinazolin-2,4-dione and 3-aryl-2-mercapto-3H-quinazolin-4-one, respectively, were prepared in good yields via efficient nucleophilic substitution reaction of the SH and NH substrates with methyl

An efficient synthesis of quinazoline-2,4-dione derivatives with the aid of a low-valent titanium reagent

A facile synthetic method using low-valent titanium reagent (TiCl4/Zn system) to promote the novel reductive cyclization of 2-nitrobenzamides and triphosgene is described. Sequentially, a series of quinazoline-2,4-diones were synthesized in goo