42044-62-2

Basic information

• Product Name: 2,3-Dimethyl-2-phenyl-buttersaeure
• Synonyms: 2,3-Dimethyl-2-phenyl-buttersaeure
• CAS NO: 42044-62-2
• Molecular Weight: 192.258
• Mol File: 42044-62-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2,3-Dimethyl-2-phenyl-buttersaeure(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-Dimethyl-2-phenyl-buttersaeure(42044-62-2)
• EPA Substance Registry System: 2,3-Dimethyl-2-phenyl-buttersaeure(42044-62-2)

Safety Data

• Hazardous Substances Data: 42044-62-2(Hazardous Substances Data)

Upstream product

• 492-37-5 hydratropic acid 
• 75-26-3 isopropyl bromide 
• 140-29-4 phenylacetonitrile 
• 5558-29-2 3-methyl-2-phenyl-butyronitrile 
• 98-86-2 acetophenone 
• 60902-63-8 2,3-dimethyl-2-phenyl-butyric acid amide 
• 29936-67-2 2,3-Dimethyl-2-phenylbutannitril 
• 64-18-6 formic acid 
• 62837-59-6 1,2-dimethyl-1-phenyl-1-propanol 

Downstream Products

• 42044-36-0 2,3-Dimethyl-2-phenyl-butaneperoxoic acid tert-butyl ester 
• 60902-68-3 2-Cyclohexyl-2,3-dimethylbuttersaeure-phenylester 
• 60902-62-7 2,3-Dimethyl-2-phenylbuttersaeure-phenylester 
• 60902-61-6 2,3-Dimethyl-2-phenylbuttersaeure-methylester 
• 60902-66-1 2,3-Dimethyl-2-phenylbutylessigsaeureester 
• 60902-73-0 Essigsaeure-(2-cyclohexyl-2,3-dimethyl)-butylester 
• 60902-67-2 2-Cyclohexyl-2,3-dimethylbuttersaeure-methylester 
• 60902-69-4 2-Cyclohexyl-2,3-dimethylbuttersaeurechlorid 
• 51556-26-4 2,3-Dimethyl-2-phenylbutylmethylketon 
• 53190-70-8 2-Cyclohexyl-2,3-dimethylbutylketon 
• 60902-65-0 (±)-2,3-dimethyl-2-phenylbutan-1-ol 
• 60902-72-9 2-Cyclohexyl-2,3-dimethylbutanol 
• 31720-72-6 2-Cyclohexyl-2,3-dimethylbuttersaeure 

Relevant articles and documents

Palladium(II)-Catalyzed C(sp2)-H Carbonylation of Sterically Hindered Amines with Carbon Monoxide

A palladium-catalyzed, amine-directed C(sp2)-H carbonylation of α,α-disubstituted benzylamine under 1 atm of CO for the facile synthesis of sterically hindered benzolactam has been developed. The key to success is the use of 2,2,6,6-tetramethyl-1-piperidinyloxy as the crucial sole oxidant. The synthetic utility of this transformation has been demonstrated by the first concise synthesis of the natural product spiropachysin-20-one.