214707-40-1

Basic information

• Product Name: Tos-Ser-OBn
• Synonyms: Tos-Ser-OBn
• CAS NO: 214707-40-1
• Molecular Weight: 349.408
• Mol File: 214707-40-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Tos-Ser-OBn(CAS DataBase Reference)
• NIST Chemistry Reference: Tos-Ser-OBn(214707-40-1)
• EPA Substance Registry System: Tos-Ser-OBn(214707-40-1)

Safety Data

• Hazardous Substances Data: 214707-40-1(Hazardous Substances Data)

Upstream product

• 60022-62-0 L-serine benzyl ester hydrochloride 
• 98-59-9 p-toluenesulfonyl chloride 
• 59524-02-6 N-tert-butoxycarbonyl-L-serine benzyl ester 

Downstream Products

• 470458-89-0 (S)-3-Hydroxy-2-[((E)-3-phenyl-allyl)-(toluene-4-sulfonyl)-amino]-propionic acid benzyl ester 
• 1738-72-3 L-serine benzyl ester 
• 470459-00-8 (R)-3-Bromo-2-[((E)-3-phenyl-allyl)-(toluene-4-sulfonyl)-amino]-propionic acid benzyl ester 
• 470458-95-8 (R)-2-[Allyl-(toluene-4-sulfonyl)-amino]-3-bromo-propionic acid benzyl ester 

Relevant articles and documents

Diastereoselective synthesis of 4-substituted L-prolines by intramolecular radical cyclization of N-aryl sulphonyl-N-allyl 3-bromoalanines: Interesting dependence of selectivity on the nature of sulphonamido groups

Enantiopure 4-substituted L-proline derivatives have been prepared via intramolecular radical cyclization of N-aryl sulphonyl-N-allyl-3-bromo-L-alanines in high yields. Surprisingly, the extent of selectivity was found to be primarily dependent on the nat