1349697-15-9

Basic information

• Product Name: C₂₁H₃₄ClNO₄Si
• CAS NO: 1349697-15-9
• Molecular Weight: 428.044
• Mol File: 1349697-15-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₂₁H₃₄ClNO₄Si(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₁H₃₄ClNO₄Si(1349697-15-9)
• EPA Substance Registry System: C₂₁H₃₄ClNO₄Si(1349697-15-9)

Safety Data

• Hazardous Substances Data: 1349697-15-9(Hazardous Substances Data)

Upstream product

• 1029529-50-7 (R,E)-N-(1-(tert-butyldimethylsilyloxy)-6-chloro-3-oxohex-4-en-2-yl)benzamide 
• 1029529-52-9 N-((2R,3S,E)-1-(tert-butyldimethylsilyloxy)-6-chloro-3-hydroxyhex-4-en-2-yl)benzamide 
• 107-30-2 chloromethyl methyl ether 
• 1029529-45-0 (R)-methyl 2-benzamido-3-(tert-butyldimethylsilyloxy)propanoate 
• 1029529-47-2 (R)-N-(3,8,8,9,9-pentamethyl-4-oxo-2,7-dioxa-3-aza-8-siladecan-5-yl)benzamide 
• 1040384-28-8 N-benzoyl-D-serine methyl ester 

Relevant articles and documents

Efficient and stereoselective syntheses of DAB-1 and D-fagomine via chiral 1,3-oxazine

The concise, stereocontrolled syntheses of DAB-1 and d-fagomine were achieved utilizing chiral oxazine. The key features in these strategies are the stereoselective intramolecular oxazine formation catalyzed by palladium(0), and pyrrolidine and piperidine formation by catalytic hydrogenation of oxazine.