61530-99-2

Basic information

• Product Name: Phosphoric acid, diethyl 2-methyl-5-(1-methylethyl)-1-cyclohexen-1-yl ester
• CAS NO: 61530-99-2
• Molecular Formula: C14H27O4P
• Molecular Weight: 290.34
• Mol File: 61530-99-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Phosphoric acid, diethyl 2-methyl-5-(1-methylethyl)-1-cyclohexen-1-yl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphoric acid, diethyl 2-methyl-5-(1-methylethyl)-1-cyclohexen-1-yl ester(61530-99-2)
• EPA Substance Registry System: Phosphoric acid, diethyl 2-methyl-5-(1-methylethyl)-1-cyclohexen-1-yl ester(61530-99-2)

Safety Data

• Hazardous Substances Data: 61530-99-2(Hazardous Substances Data)

Upstream product

• 64474-56-2 (+)-9-bromocamphor 
• 814-49-3 diethyl chlorophosphate 
• 85719-15-9 (+)-endo-3,9-dibromocamphor 
• 10293-06-8 (1R)-3-endo-bromocamphor 
• 464-49-3 (1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one 
• 499-70-7 carvomenthone 

Downstream Products

• 1195-31-9 (+)-p-menth-1-ene 

Relevant articles and documents

Synthesis and Absolute Configuration of the Antiparasitic Furanosesquiterpenes (-)-Furodysin and (-)-Furodysinin. Camphor as a Six-Membered Ring Chiral Pool Template

The syntheses of (-)-furodysin ((-2)-2a) and (-)-furodysinin ((-)-3a) in four steps starting from (+)-9-bromocamphor (18) has been accomplished, thus establishing the absolute configuration of these and related metabolites.This was made possible by the unexpected exo selectivity in the aldol condensation of camphor-like enolates with aldehydes.This has been found to be a general phenomenon in the camphor system.Further, anionic fragmentation of the C1-C7 bond of camphor derivatives has allowed access to synthetic intermediates containing functionalized six-memberedrings, thus opening up avenues from camphor to a new class of chiral pool elements not currently available from chiral pool substances.