824402-15-5

Basic information

• Product Name: 1,4-Dioxaspiro[4.14]nonadecane-2,3-dicarboxamide, 7-methyl-N,N'-bis(phenylmethyl)-, (2R,3R,7R)-
• CAS NO: 824402-15-5
• Molecular Formula: C34H48N2O4
• Molecular Weight: 548.766
• Mol File: 824402-15-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1,4-Dioxaspiro[4.14]nonadecane-2,3-dicarboxamide, 7-methyl-N,N'-bis(phenylmethyl)-, (2R,3R,7R)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-Dioxaspiro[4.14]nonadecane-2,3-dicarboxamide, 7-methyl-N,N'-bis(phenylmethyl)-, (2R,3R,7R)-(824402-15-5)
• EPA Substance Registry System: 1,4-Dioxaspiro[4.14]nonadecane-2,3-dicarboxamide, 7-methyl-N,N'-bis(phenylmethyl)-, (2R,3R,7R)-(824402-15-5)

Safety Data

• Hazardous Substances Data: 824402-15-5(Hazardous Substances Data)

Upstream product

• 107442-24-0 (R)-(+)-3-methylhexadecanedioic acid 
• 869683-45-4 (R)-di-benzyl 3-methylhexadecanedioate 
• 10403-00-6 (R)-3-methyl-1-cyclopentadecanone 
• 88393-56-0 (2R,3R)-N¹,N⁴-dibenzyl-2,3-dihydroxysuccinamide 
• 956-82-1 3-methylcyclopentadecanone 

Downstream Products

• 10403-00-6 (R)-3-methyl-1-cyclopentadecanone 

Relevant articles and documents

A simplified synthesis of (R)-(-)-muscone using a ring-opening reaction of (R)-(+)-β-methyl-β-propiolactone

A chiral macrocyclic precursor can be constructed via a ring-opening reaction of (R)-(+)-β-methyl-β-propiolactone with a functionalized organocuprate with no loss of enantiomeric excess. The carboxylic acid precursor was used as a chiral building block for the synthesis of chiral muscone and musky macrolactones.