107134-90-7

Basic information

• Product Name: 1-<(4-Methylphenyl)(trimethylsilyloxy)methyl>pyridinium-trifluormethansulfonat
• CAS NO: 107134-90-7
• Molecular Weight: 421.513
• Mol File: 107134-90-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-<(4-Methylphenyl)(trimethylsilyloxy)methyl>pyridinium-trifluormethansulfonat(CAS DataBase Reference)
• NIST Chemistry Reference: 1-<(4-Methylphenyl)(trimethylsilyloxy)methyl>pyridinium-trifluormethansulfonat(107134-90-7)
• EPA Substance Registry System: 1-<(4-Methylphenyl)(trimethylsilyloxy)methyl>pyridinium-trifluormethansulfonat(107134-90-7)

Safety Data

• Hazardous Substances Data: 107134-90-7(Hazardous Substances Data)

Upstream product

• 84355-13-5 N-Trimethylsilylpyridinium trifluoromethanesulfonate 
• 104-87-0 4-methyl-benzaldehyde 

Downstream Products

• 128816-30-8 1-(4-methylphenyl)ethyl trimethylsilyl ether 
• 96258-65-0 diethyl α-trimethylsilyloxy-4-methylbenzylphosphonate 
• 18544-88-2 (p-Tolyl-trimethylsilanyloxy-methyl)-phosphonic acid dimethyl ester 
• 107134-94-1 (4-methylphenyl)<(trimethylsiloxy)methyl>triphenylphosphonium trifluoromethanesulfonate 
• 128816-27-3 Trimethyl-(phenylsulfanyl-p-tolyl-methoxy)-silane 
• 128816-28-4 1-(p-Tolyl-trimethylsilanyloxy-methyl)-1H-pyrrole 
• 128816-29-5 2-(p-Tolyl-trimethylsilanyloxy-methyl)-malonic acid diethyl ester 
• 66985-49-7 2-(4-methylphenyl)-2-(trimethylsilyloxy)acetonitrile 
• 142821-31-6 oxybis<(4-methylphenyl)(1-pyridino)methane> bis(trifluoromethanesulfonate) 
• 128816-22-8 Trifluoro-methanesulfonatetributyl-(p-tolyl-trimethylsilanyloxy-methyl)-phosphonium; 
• 128816-31-9 trimethyl(phenyl(p-tolyl)methoxy)silane 
• 107134-92-9 4-Benzyl-1-<(4-methylphenyl)(trimethylsilyloxy)methyl>pyridinium-trifluormethansulfonat 

Relevant articles and documents

Syntheses with N-Trimethylsilylheteroarylium Salts: Reactions with Aldehydes, Ketones and Carboxylic Acids. Comparison of Reactivity with Analogous N-Acylheteroarylium Salts

N-Trimethylsilylheteroarylium salts 2 can be characterized as efficient silylating reagents for carbonyl compounds (5 or 8) and carbonic acids 11, their reactivity is comparable to that of N-acylheteroarylium salts 1.In some cases (depending on the nature of the substrates), their silylating power can be stronger than the acylating power of comparable salts 1.This will be demonstrated in the case of enolizable examples of 5 and 8.