3528-23-2

Usage

Structure

Contains a benzene ring fused to a pyrone ring

Natural Sources

Found in tonka beans, cinnamon, sweet clover, and other plant species

Applications

Used in the production of perfumes and flavorings due to its pleasant, sweet scent
Acts as a precursor to the drug warfarin in medicine, owing to its anticoagulant properties

Regulation

Its use in food and beverages is regulated in several countries due to potential liver damage associated with excessive consumption

Versatility

Widely used in fragrance, flavor, and medicine industries

Upstream product

• 93416-98-9 3-Bromo-4-oxo-2,3-dihydro-4H-naphtho<1,2-b>pyran 
• 26060-30-0 4-nitrothiobenzamide 
• 2521-24-6 4-chlorothiobenzamide 
• 2227-79-4 benzenecarbothioamide 
• 61019-26-9 4-Amino-5-(o-methoxyphenyl)-3(4H)-1,2,4-triazolethione 
• 22706-11-2 3-phenyl-4-amino-5-mercapto-1,2,4-triazole 
• 68468-95-1 4-amino-5-mercapto-3-(4-chlorophenyl)-1,2,4-triazole 
• 36209-50-4 4-amino-5-(4-nitrophenyl)-1,2,4-triazole-3-thiol 

Downstream Products

• 64-18-6 formic acid 
• 1354628-16-2 2-(3-methyl-1-phenyl-1H-pyrazolo[3,4-b]pyridin-6-yl)naphthalen-1-ol 
• 1354628-17-3 5-(1-hydroxynaphthalen-2-yl)-1-methyl-3-phenyl-1H-imidazo[4,5-b]pyridine-2(3H)-thione 
• 1251738-89-2 2-cyclohexyl-4H-benzo[h]chromen-4-one 
• 1413433-55-2 C₁₉H₁₄O₂ 
• 6051-86-1 2-phenyl-2H-benzo[h]chromen-4(3H)-one 

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