150075-20-0

Basic information

• Product Name: 1,5-Pentanediol, 1-(4-methoxyphenyl)-
• CAS NO: 150075-20-0
• Molecular Formula: C12H18O3
• Molecular Weight: 210.273
• Mol File: 150075-20-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1,5-Pentanediol, 1-(4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,5-Pentanediol, 1-(4-methoxyphenyl)-(150075-20-0)
• EPA Substance Registry System: 1,5-Pentanediol, 1-(4-methoxyphenyl)-(150075-20-0)

Safety Data

• Hazardous Substances Data: 150075-20-0(Hazardous Substances Data)

Upstream product

• 108-55-4 glutaric anhydride, 
• 100-66-3 methoxybenzene 
• 4609-10-3 5-(4-methoxyphenyl)-5-oxopentanoic acid 
• 1847-68-3 5-(4-methoxy-phenyl)-5-oxo-pentanoic acid methyl ester 

Downstream Products

• 132723-33-2 2-(4-methoxyphenyl)-tetrahydro-2H-pyran 
• 25882-27-3 5-hydroxy-1-(4-methoxyphenyl)pentan-1-one 

Relevant articles and documents

Aryl Boronic Acid Catalysed Dehydrative Substitution of Benzylic Alcohols for C?O Bond Formation

A combination of pentafluorophenylboronic acid and oxalic acid catalyses the dehydrative substitution of benzylic alcohols with a second alcohol to form new C?O bonds. This method has been applied to the intermolecular substitution of benzylic alcohols to form symmetrical ethers, intramolecular cyclisations of diols to form aryl-substituted tetrahydrofuran and tetrahydropyran derivatives, and intermolecular crossed-etherification reactions between two different alcohols. Mechanistic control experiments have identified a potential catalytic intermediate formed between the aryl boronic acid and oxalic acid.