1379820-13-9

Basic information

• Product Name: 4-p-methylphenyl-1,2-oxaborol-2(5H)-ol
• Synonyms: 4-p-methylphenyl-1,2-oxaborol-2(5H)-ol
• CAS NO: 1379820-13-9
• Molecular Weight: 174.007
• Mol File: 1379820-13-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-p-methylphenyl-1,2-oxaborol-2(5H)-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-p-methylphenyl-1,2-oxaborol-2(5H)-ol(1379820-13-9)
• EPA Substance Registry System: 4-p-methylphenyl-1,2-oxaborol-2(5H)-ol(1379820-13-9)

Safety Data

• Hazardous Substances Data: 1379820-13-9(Hazardous Substances Data)

Upstream product

• 5419-55-6 Triisopropyl borate 
• 107-19-7 propargyl alcohol 

Downstream Products

• 1489100-10-8 2-(4-p-tolyl-2,5-dihydrofuran-2-yl)phenol 
• 143360-75-2 2-methyl-4-(4'-methylphenyl)furan 
• 344339-78-2 C₁₇H₁₃ClO 
• 344350-71-6 4-(4-methylphenyl)-2-phenylfuran 
• 1418224-46-0 (Z)-4-phenyl-2-p-tolylbut-2-en-1-ol 
• 1418224-47-1 (Z)-4-(4-nitrophenyl)-2-p-tolylbut-2-en-1-ol 

Relevant articles and documents

One-pot synthesis of functionalized 2,5-dihydrofurans via an amine-promoted Petasis borono-Mannich reaction

A series of functionalized 2,5-dihydrofurans were efficiently synthesized via an amine-promoted Petasis borono-Mannich reaction of 4-substituted 1,2-oxaborol-2(5H)-ols with salicylaldehydes in high yields. The process, which combines a boronic acid-based Mannich reaction and a highly efficient intramolecular SN2 cyclization, provides a one-step and efficient route toward 2,5-dihydrofurans from simple and stable starting materials.