228115-40-0

Basic information

• Product Name: .beta.-D-Gulopyranose, 3-amino-1,6-anhydro-3-deoxy-, 4-acetate 2-(dihydrogen phosphate)
• Synonyms: .beta.-D-Gulopyranose, 3-amino-1,6-anhydro-3-deoxy-, 4-acetate 2-(dihydrogen phosphate)
• CAS NO: 228115-40-0
• Molecular Formula: C8H14 N O8 P
• Molecular Weight: 283.17
• Mol File: 228115-40-0.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: .beta.-D-Gulopyranose, 3-amino-1,6-anhydro-3-deoxy-, 4-acetate 2-(dihydrogen phosphate)(CAS DataBase Reference)
• NIST Chemistry Reference: .beta.-D-Gulopyranose, 3-amino-1,6-anhydro-3-deoxy-, 4-acetate 2-(dihydrogen phosphate)(228115-40-0)
• EPA Substance Registry System: .beta.-D-Gulopyranose, 3-amino-1,6-anhydro-3-deoxy-, 4-acetate 2-(dihydrogen phosphate)(228115-40-0)

Safety Data

• Hazardous Substances Data: 228115-40-0(Hazardous Substances Data)

Upstream product

• 228115-46-6 1,6-anhydro-3-(N,N-dibenzylamino)-3-deoxy-4-O-(2-tetrahydropyranyl)-β-D-gulopyranose 2-(o-xylylene phosphate) 
• 228115-47-7 1,6-anhydro-3-(N,N-dibenzylamino)-3-deoxy-β-D-gulopyranose 2-(o-xylylene phosphate) 
• 228115-45-5 1,6-anhydro-3-(N,N-dibenzylamino)-3-deoxy-4-O-(2-tetrahydropyranyl)-β-D-gulopyranose 
• 228115-43-3 1,6-anhydro-3-N-benzylamino-2-O,3-N-carbonyl-3-deoxy-4-O-(2-tetrahydropyranyl)-β-D-gulopyranose 
• 228115-44-4 3-amino-1,6-anhydro-3-N-benzyl-3-deoxy-4-O-(2-tetrahydropyranyl)-β-D-gulopyranose 
• 228115-42-2 1,6-anhydro-3-N-benzylamino-2-O,3-N-carbonyl-3-deoxy-β-D-gulopyranose 
• 228115-41-1 3-amino-1,6-anhydro-3-N-tert-butoxycarbonyl-3-deoxy-β-D-gulopyranose 
• 127903-51-9 (2R)-[1,3]dioxolane-2r,4c-dicarbaldehyde 
• 116607-29-5 1,6-anhydro-3-deoxy-3-nitro-β-D-gulopyranose 
• 228115-48-8 4-O-acetyl-1,6-anhydro-3-(N,N-dibenzylamino)-3-deoxy-β-D-gulopyranose 2-(o-xylylene phosphate) 
• 108782-66-7 3-amino-1,6-anhydro-3-deoxy-β-D-gulopyranose hydrochloride 

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