882687-75-4

Usage

Chemical class

Naphthopyranones

Structure

Bromine atom at the 7th position on the pyran ring

Potential applications

Medicinal chemistry and drug development

Biological activities

Antimicrobial, antifungal, antitumor properties
Modulation of chemical reactivity and pharmacological profile
Need for further research to explore full potential uses and effects

Upstream product

• 882687-64-1 3,7-dibromo-2,3-dihydro-4H-naphtho[1,2-b]pyran-4-one 
• 78027-00-6 4-amino-5-(3-pyridyl)-4H-1,2,4-triazole-3-thiol 
• 36209-50-4 4-amino-5-(4-nitrophenyl)-1,2,4-triazole-3-thiol 
• 68468-95-1 4-amino-5-mercapto-3-(4-chlorophenyl)-1,2,4-triazole 
• 22706-11-2 3-phenyl-4-amino-5-mercapto-1,2,4-triazole 
• 61019-26-9 4-Amino-5-(o-methoxyphenyl)-3(4H)-1,2,4-triazolethione 
• 62-55-5 thioacetamide 
• 17356-08-0 thiourea 
• 2227-79-4 benzenecarbothioamide 
• 97625-36-0 7-Bromo-4-oxo-2,3-dihydro-4H-naphtho<1,2-b>pyran 
• 26060-30-0 4-nitrothiobenzamide 
• 2521-24-6 4-chlorothiobenzamide 

Relevant academic research and scientific papers

Synthesis and antibacterial studies of 6-aryl-2,2a-dihydro-naphtho- [2′,1′-5,6]pyrano[4,3-e][1,2,4]triazolo[3,4-b][1,3,4]thiadiazine and its derivatives

Chemoselective synthesis of novel hetero cyclopenta[b]chrysene derivatives, namely, 6-Aryl-2,2a-dihydro-naphtho[2′,1′,5,6]pyrao[4,3-e][1,2,4] triazolo[3,4-b][1,3,4]thiadiazine (4a-j) under neutral condition has been described. These molecules exhibited go

Chemoselective synthesis of hetero cyclic derivatives of 18-nor equilenine, 16-substituted-12H-11-oxa-15-aza-17-thia-cyclopenta[a] phenanthrenene and their in vitro evaluation of antibacterial and antifungal activity

Chemoselective synthesis of heterocyclic derivatives of 18-norequilenine, 16-substituted-12H-11-oxa-15-aza-17-thiacyclopenta[a]phenanthrene 4a-j is presented. These molecules 4a-j have exhibited moderate to good antibacterial activity against some gram-po