16463-42-6

Basic information

• Product Name: Benzoic acid, 2,6-dimethoxy-, potassium salt
• CAS NO: 16463-42-6
• Molecular Formula: C9H10O4.K
• Molecular Weight: 220.266
• Mol File: 16463-42-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 2,6-dimethoxy-, potassium salt(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 2,6-dimethoxy-, potassium salt(16463-42-6)
• EPA Substance Registry System: Benzoic acid, 2,6-dimethoxy-, potassium salt(16463-42-6)

Safety Data

• Hazardous Substances Data: 16463-42-6(Hazardous Substances Data)

Upstream product

• 1466-76-8 2-6-dimethoxybenzoic acid 

Downstream Products

• 27124-92-1 2',6'-dimethoxy-2,3,4,5-tetrahydro-1,1'-biphenyl 
• 634-36-6 1,2,3-trimethoxybenzene 

Relevant articles and documents

Arylalkene synthesis via decarboxylative cross-coupling of alkenyl halides

A bimetallic catalyst system generated from readily available palladium(II) and copper(I) salts, 1,10-phenanthroline and tri-1-naphthylphosphine was found to efficiently mediate the decarboxylative cross-coupling of alkenyl bromides and chlorides with aromatic carboxylates. It allows the regiospecific synthesis of a broad range of aryl- and heteroarylalkenes in high yields.

Low-Temperature Ag/Pd-catalyzed decarboxylative cross-coupling of aryl trflates with aromatic carboxylate salts

Chemical Equation Presented At 50°C lower than the best known copper catalysts, a catalytic silver(I)/ palladium(II) system allows the decarboxylative cross-coupling of arenecarboxylates with aryl triflates at temper-atures as low as 120°C. Remarkably, polychlorinated and many heterocyclic arenecarboxylates are converted for the first time in high yields. FG = functional group.