876950-23-1

Basic information

• Product Name: D-Proline, 3-hydroxy-4-methyl-2-[(1S)-2-methyl-1-(phenylmethoxy)propyl]-5-oxo-, (3S,4S)-
• CAS NO: 876950-23-1
• Molecular Formula: C17H23NO5
• Molecular Weight: 335.357
• Mol File: 876950-23-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: D-Proline, 3-hydroxy-4-methyl-2-[(1S)-2-methyl-1-(phenylmethoxy)propyl]-5-oxo-, (3S,4S)-(CAS DataBase Reference)
• NIST Chemistry Reference: D-Proline, 3-hydroxy-4-methyl-2-[(1S)-2-methyl-1-(phenylmethoxy)propyl]-5-oxo-, (3S,4S)-(876950-23-1)
• EPA Substance Registry System: D-Proline, 3-hydroxy-4-methyl-2-[(1S)-2-methyl-1-(phenylmethoxy)propyl]-5-oxo-, (3S,4S)-(876950-23-1)

Safety Data

• Hazardous Substances Data: 876950-23-1(Hazardous Substances Data)

Upstream product

• 1125-88-8 benzaldehyde dimethyl acetal 
• 89459-98-3 (2S,3S)-2,3-epoxy-4-methyl-1-pentanol 
• 876950-16-2 (3R,4R,5S,6S,8R)-6-isopropyl-3-methyl-8-phenyl-7,9,11,13-tetraoxa-12-thiocarbonyl-1-azaspiro[4.5]decan-2-one 
• 876950-18-4 (3R,4R,5S,6S,8R)-3,4-dihydroxy-6-isopropyl-3-methyl-8-phenyl-7,9-dioxa-1-azaspiro[4.5]decan-2-one 
• 876950-22-0 benzoic acid (S)-1-((2S,3S,4S)-3-hydroxymethyl-4-methyl-5-oxo-pyrrolidin-2-yl)-2-methylpropyl ester 
• 876950-21-9 (3S,4S,5S,6S,8R)-4-hydroxy-6-isopropyl-3-methyl-8-phenyl-7,9-dioxa-1-azaspiro[4.5]decan-2-one 
• 876950-17-3 1-chloro-6-isopropyl-3-methyl-8-phenyl-7,9-dioxa-1-aza-spiro[4.5]dec-3-en-2-one 
• 876950-19-5 (5R,6S,8R)-6-isopropyl-3-methyl-8-phenyl-7,9-dioxa-1-azaspiro[4.5]dec-3-en-2-one 
• 870527-61-0 (E)-(2R,4S,5R)-(-)-(3-bromo-2-methyl-allyl)-(4-isopropyl-2-phenyl-[1,3]dioxan-5-yl)-amine 
• 870527-60-9 (5R,6S,8R)-(-)-6-isopropyl-3-methyl-8-phenyl-7,9-dioxa-1-azaspiro[4.5]dec-3-ene 
• 870527-70-1 (2R,4S,5R)-(-)-5-azido-4-isopropyl-2-phenyl[1,3]dioxane 
• 870527-58-5 (2R,4S,5R)-(-)-5-amino-4-isopropyl-2-phenyl[1,3]dioxane 
• 876950-24-2 (S)-1-((2S,3S,4S)-2-formyl-3-hydroxy-4-methyl-5-oxo-pyrrolidin-2-yl)-2-methyl-propyl benzoate 

Downstream Products

• 186833-31-8 7-epi-omuralide 

Relevant articles and documents

Enantioselective total syntheses of omuralide, 7-epi-omuralide, and (+)-lactacystin

(Chemical Equation Presented) An alkylidene carbene 1,5-CH insertion has been used as a key step in an enantioselective total syntheses of omuralide, its C7-epimer, and (+)-lactacystin. An additional noteworthy feature of the synthesis is the use of a nov