228115-94-4

Basic information

• Product Name: L-glycero-L-galacto-Heptitol, 2,6-anhydro-1,3:5,7-bis-O-(phenylmethylene)-, 4-methylbenzenesulfonate
• Synonyms: L-glycero-L-galacto-Heptitol, 2,6-anhydro-1,3:5,7-bis-O-(phenylmethylene)-, 4-methylbenzenesulfonate
• CAS NO: 228115-94-4
• Molecular Formula: C₂₈H₂₈O₈S
• Molecular Weight: 524.58
• Mol File: 228115-94-4.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: L-glycero-L-galacto-Heptitol, 2,6-anhydro-1,3:5,7-bis-O-(phenylmethylene)-, 4-methylbenzenesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: L-glycero-L-galacto-Heptitol, 2,6-anhydro-1,3:5,7-bis-O-(phenylmethylene)-, 4-methylbenzenesulfonate(228115-94-4)
• EPA Substance Registry System: L-glycero-L-galacto-Heptitol, 2,6-anhydro-1,3:5,7-bis-O-(phenylmethylene)-, 4-methylbenzenesulfonate(228115-94-4)

Safety Data

• Hazardous Substances Data: 228115-94-4(Hazardous Substances Data)

Upstream product

• 52443-07-9 3,4,5,7-tetra-O-acetyl-2,6-anhydro-D-glycero-L-manno-heptonitrile 
• 228115-82-0 3,4,7-tri-O-acetyl-2,6-anhydro-D-glycero-L-manno-heptonic acid 
• 228115-81-9 Acetic acid (1S,4R,6R,7S,8R)-8-acetoxy-6-acetoxymethyl-3-oxo-2,5-dioxa-bicyclo[2.2.2]oct-7-yl ester 
• 71420-08-1 1,3-diphenyl-2-(tetra-O-acetyl-2,6-anhydro-D-glycero-L-manno-heptosyl)imidazolidine 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 71420-09-2 2,3,4,6-tetra-O-acetyl-2,6-anhydro-D-glycero-L-manno-heptose 
• 115224-88-9 1,3,4,5,7-penta-O-acetyl-2,6-anhydro-L-glycero-L-galacto-heptitol 
• 13964-15-3 2,6-anhydro-L-glycero-L-galacto-heptitol 
• 71072-12-3 (4aS,8aR,9R,9aR,10aR)-2,7-Diphenyl-hexahydro-1,3,6,8,10-pentaoxa-anthracen-9-ol 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 71072-13-4 Acetic acid (4aS,8aS,9R,9aS,10aR)-2,7-diphenyl-hexahydro-1,3,6,8,10-pentaoxa-anthracen-9-yl ester 
• 71072-12-3 (4aS,8aR,9R,9aR,10aR)-2,7-Diphenyl-hexahydro-1,3,6,8,10-pentaoxa-anthracen-9-ol 
• 228115-96-6 2,6-anhydro-4-azido-1,3:5,7-di-O-benzylidene-4-deoxy-L-glycero-L-gluco-heptitol 

Relevant articles and documents

Synthesis studies of structural analogues of tagetitoxin: 4-O-acetyl-3- amino-1,6-anhydro-3-deoxy-D-gulose 2-phosphate

Synthetic approaches to structural analogues of tagetitoxin (1) are described. The successful route to analogue 3 (X=O) has, as a key step, protection of the cis-vicinal amino alcohol moiety of compound 7 as an N- benzylated cyclic carbamate (9). X-Ray cr