14643-62-0

Basic information

• Product Name: tris(p-methylphenyl) borate
• Synonyms: tris(p-methylphenyl) borate
• CAS NO: 14643-62-0
• Molecular Weight: 332.207
• Mol File: 14643-62-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: tris(p-methylphenyl) borate(CAS DataBase Reference)
• NIST Chemistry Reference: tris(p-methylphenyl) borate(14643-62-0)
• EPA Substance Registry System: tris(p-methylphenyl) borate(14643-62-0)

Safety Data

• Hazardous Substances Data: 14643-62-0(Hazardous Substances Data)

Upstream product

• 106-44-5 p-cresol 
• 5337-36-0 trihexyl borate 
• 11113-50-1 boric acid 

Downstream Products

• 101-94-0 p-tolyl phenylacetate 
• 229007-98-1 N-methyl-N-methoxy-5-(4-methylphenyl)furan-2-carboxamide 
• 229006-96-6 7-(4-methylphenyl)-2,3-dihydro-1-benzooxepine-4-carboxylic acid 
• 610273-86-4 (R)-3-p-tolyl-cyclohexanone 
• 5459-79-0 N,N-dibenzyl-4-methylbenzenamine 
• 897961-09-0 2-phenyl-2-(2-hydroxy-5-methylphenyl)-N-(4-methylphenylsulfonyl)-ethanamine 
• 99429-99-9 4-methylphenyl (2E)-3-phenylprop-2-enoate 
• 229009-16-9 tert-butyl 1-methyl-7-(4-methylphenyl)-2,3-dihydro-1-benzoazepine-4-carboxylate 
• 229008-89-3 ethyl 6-(4-methylphenyl)-1,2-dihydro-2H-thiochromene-3-carboxylate 
• 229008-14-4 N-methyl-N-methoxy-5-(4-methylphenyl)pyridine-3-carboxamide 
• 229007-97-0 (E)-3-[5-(4-methylphenyl)-thiophen-2-yl]acrylic acid 

Relevant articles and documents

Synthesis and antioxidant characteristics of borate esters used in lubricating oil

In the present studies, the preparation of esters of boric acid with hindered phenols is reported, wherein the alkyl groups are branched on the α-carbon atoms. The products were evaluated in terms of their oxidative stability. In most cases, improvements in oxidative stability in ahydrocarbon media (cumene) were observed.

A new regio- and stereoselective intermolecular Friedel-Crafts alkylation of phenolic substrates with aryl epoxides

A conceptually new regioselective and highly syn-stereoselective intermolecular Friedel-Crafts-type O-alkylation of phenols with aryl epoxides by the use of appropriately substituted aryl borates is reported. The carbon-carbon bond formation occurs in neutral and mild conditions without the need for external Lewis acids or transition metal catalysts.