212915-61-2

Basic information

• Product Name: 2,2-Dimethyl-propionic acid (1S,2S,3S)-3-isopropenyl-2-methyl-2-(2-phenylselanylcarbonyl-ethyl)-cyclopentyl ester
• CAS NO: 212915-61-2
• Molecular Weight: 435.465
• Mol File: 212915-61-2.mol

Chemical Properties

• CAS DataBase Reference: 2,2-Dimethyl-propionic acid (1S,2S,3S)-3-isopropenyl-2-methyl-2-(2-phenylselanylcarbonyl-ethyl)-cyclopentyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2-Dimethyl-propionic acid (1S,2S,3S)-3-isopropenyl-2-methyl-2-(2-phenylselanylcarbonyl-ethyl)-cyclopentyl ester(212915-61-2)
• EPA Substance Registry System: 2,2-Dimethyl-propionic acid (1S,2S,3S)-3-isopropenyl-2-methyl-2-(2-phenylselanylcarbonyl-ethyl)-cyclopentyl ester(212915-61-2)

Safety Data

• Hazardous Substances Data: 212915-61-2(Hazardous Substances Data)

Upstream product

• 71098-88-9 N-phenylselanylphthalimide 
• 212915-60-1 2,2-Dimethyl-propionic acid (1S,2S,3S)-2-(2-carboxy-ethyl)-3-isopropenyl-2-methyl-cyclopentyl ester 
• 212953-00-9 (1S,7aS)-(+)-1-hydroxy-4,7a-dimethyl-2,3,7,7a-tetrahydro-1H-indene-5⁽⁶⁾-one 
• 33878-96-5 (7aS)-(+)-4,7a-dimethyl-2,3,7,7a-tetrahydro-1H-indene-1,5(6H)-dione 
• 212915-50-9 2,2-Dimethyl-propionic acid (1S,5S,7aS)-5-hydroxy-4,7a-dimethyl-2,3,5,6,7,7a-hexahydro-1H-inden-1-yl ester 
• 212915-49-6 2,2-Dimethyl-propionic acid (1S,7aS)-4,7a-dimethyl-5-oxo-2,3,5,6,7,7a-hexahydro-1H-inden-1-yl ester 
• 212915-59-8 2,2-Dimethyl-propionic acid (1S,2S,3S)-3-isopropenyl-2-(2-methoxycarbonyl-ethyl)-2-methyl-cyclopentyl ester 
• 212915-52-1 2,2-Dimethyl-propionic acid (3aS,5aS,6S,8bR)-2,2,5a,8b-tetramethyl-decahydro-indeno[4,5-d][1,2]oxasilol-6-yl ester 
• 212915-57-6 2,2-Dimethyl-propionic acid (1S,2S,3R)-3-((S)-1,2-dihydroxy-1-methyl-ethyl)-2-(2-methoxycarbonyl-ethyl)-2-methyl-cyclopentyl ester 
• 212915-58-7 2,2-Dimethyl-propionic acid (1S,2S,3R)-2-(2-methoxycarbonyl-ethyl)-2-methyl-3-((S)-4-methyl-2-thioxo-[1,3]dioxolan-4-yl)-cyclopentyl ester 
• 212915-53-2 2,2-Dimethyl-propionic acid (1S,3aR,4S,5S,7aS)-5-hydroxy-4-hydroxymethyl-4,7a-dimethyl-octahydro-inden-1-yl ester 

Relevant articles and documents

Novel and general entry into pseudoguaianolides. Formal and enantioselective synthesis of (+)-confertin

A novel and general access to pseudoguaianolide sesquiterpenoids has been developed by employing a diastereoselective acyl radical-mediated 7- endo-trigonal mode of cyclization as a key reaction step. The methodology has successfully been applied to the formal enantioselective synthesis of (+)- confertin.