1260677-75-5

Basic information

• Product Name: 1-(1,3-benzodioxol-5-yl)-3-(2-bromophenyl)propan-1-one
• Synonyms: 1-(1,3-benzodioxol-5-yl)-3-(2-bromophenyl)propan-1-one
• CAS NO: 1260677-75-5
• Molecular Weight: 333.181
• Mol File: 1260677-75-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-(1,3-benzodioxol-5-yl)-3-(2-bromophenyl)propan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(1,3-benzodioxol-5-yl)-3-(2-bromophenyl)propan-1-one(1260677-75-5)
• EPA Substance Registry System: 1-(1,3-benzodioxol-5-yl)-3-(2-bromophenyl)propan-1-one(1260677-75-5)

Safety Data

• Hazardous Substances Data: 1260677-75-5(Hazardous Substances Data)

Upstream product

• 847922-60-5 C₁₆H₁₁BrO₃ 
• 5208-87-7 1'-hydroxysafrole 
• 583-55-1 1-Bromo-2-iodobenzene 

Downstream Products

• 250660-51-6 2-(benzo[d][1,3]dioxol-5-yl)chromane 
• 1384560-04-6 1-(benzo[d][1,3]-dioxol-5-yl)-3-(2-bromophenyl)propan-1-ol 
• 1384560-12-6 2-(benzo[d][1,3]dioxol-5-yl)-4-(2-bromophenyl)butan-2-ol 
• 1449789-83-6 3-(1,3-benzodioxol-5-yl)-1-(2-bromophenyl)hex-5-en-3-ol 
• 1449789-82-5 3-(1,3-benzodioxol-5-yl)-5-(2-bromophenyl)pent-1-en-3-ol 

Relevant articles and documents

Lewis Acid Mediated Domino Intramolecular Cyclization: Synthesis of Dihydrobenzo[ a]fluorenes

An efficient and facile method for the regioselective synthesis of novel dihydrobenzo[a]fluorenes from readily accessible alkynols is presented. The current strategy triggers the formation of a dual C-C bond intramolecularly via Lewis acid catalysis under mild reaction conditions. Notably, secondary as well as tertiary alcohols bearing an alkyne moiety have been smoothly transformed into the corresponding products. As a result, novel tetracyclic dihydrobenzo[a]fluorenes have been accomplished using this approach.

Transition metals catalyzed C-C and C-O bonds formation: Facile synthesis of flavans and benzoxepines

A simple and practical method has been developed based on intermolecular [Pd]-catalyzed C-C and an intramolecular [Cu]-catalyzed C-O bond formations for the synthesis of flavans and benzoxepines. Interestingly, the method is amenable for the synthesis of