32783-79-2

Basic information

• Product Name: Propanal, 3-(benzoyloxy)-2,2-dimethyl-
• CAS NO: 32783-79-2
• Molecular Formula: C12H14O3
• Molecular Weight: 206.241
• Mol File: 32783-79-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Propanal, 3-(benzoyloxy)-2,2-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Propanal, 3-(benzoyloxy)-2,2-dimethyl-(32783-79-2)
• EPA Substance Registry System: Propanal, 3-(benzoyloxy)-2,2-dimethyl-(32783-79-2)

Safety Data

• Hazardous Substances Data: 32783-79-2(Hazardous Substances Data)

Upstream product

• 126-30-7 2,2-Dimethyl-1,3-propanediol 
• 98-88-4 benzoyl chloride 
• 5522-92-9 2,2-dimethyl-1,3-propanediol 1-benzoate 
• 90839-63-7 (2R)-1,1,3,3-tetramethyl-1,2,4-butanetriol 1-benzoate 

Downstream Products

• 1416254-77-7 2,2-dimethylbut-3-en-1-yl benzoate 
• 100-51-6 benzyl alcohol 
• 90839-64-8 Benzoic acid 3-methanesulfonyloxy-2,2-dimethyl-propyl ester 
• 75-84-3 2,2-dimethyl-propanol-1 
• 5522-92-9 2,2-dimethyl-1,3-propanediol 1-benzoate 
• 1416254-81-3 2,2-dimethyloctyl benzoate 

Relevant articles and documents

Dithiocarbamate-substituted gem-difluorinated silicon reagent: generation and addition to aldehydes

Abstract A new gem-difluorinated silicon reagent bearing a pyrrolidine dithiocarbamate substituent was prepared by the reaction of (bromodifluoromethyl)trimethylsilane with the corresponding potassium dithiocarbamate. The obtained reagent was employed in

SUBSTITUTED PYRAZOLOAZEPIN-4-ONES AND THEIR USE AS PHOSPHODIESTERASE INHIBITORS

The present invention relates to novel substituted pyrazoloazepin-4-ones with phosphodiesterase inhibitory activity, as well as to their use as therapeutic agents the treatment of inflammatory diseases and conditions.

Steric Course of N5,N10-Methylenetetrahydrofolate Formation from Glycine by the Glycine Cleavage System in E. coli

The steric course of the conversion of glycine to 5,10-methylenetetrahydrofolate (5,10-CH2-H4folate) by the glycine cleavage system in E. coli has been elucidated. 2-Hre of glycine is the precursor of 11-Hre of 5,10-CH2-H4folate, and 2-Hsi of glycine is the precursor of 11-Hsi of 5,10-CH2-H4folate.The overall transformation is at least 78percent stereospecific (possibly higher).