21090-79-9

Basic information

• Product Name: 3,6-anhydro-D-talo-2-heptulose phenylosazone
• CAS NO: 21090-79-9
• Molecular Weight: 370.408
• Mol File: 21090-79-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 3,6-anhydro-D-talo-2-heptulose phenylosazone(CAS DataBase Reference)
• NIST Chemistry Reference: 3,6-anhydro-D-talo-2-heptulose phenylosazone(21090-79-9)
• EPA Substance Registry System: 3,6-anhydro-D-talo-2-heptulose phenylosazone(21090-79-9)

Safety Data

• Hazardous Substances Data: 21090-79-9(Hazardous Substances Data)

Upstream product

• 3624-30-4 D-galacto-2-heptulose phenylosazone 
• 3624-30-4 D-manno-hept-2-ulose phenylosazone 
• 3624-30-4 D-gluco-hept-2-ulose phenylosazone 
• 3624-30-4 D-altro-2-heptulose phenylosazone 
• 73364-67-7 D-galacto-heptulose phenylosazone 

Downstream Products

• 74134-95-5 4-α-D-arabinofuranosyl-2-phenyl-1,2,3-osotriazole 
• 74211-21-5 2-phenyl-4-(2,3,5-tri-O-acetyl-β-D-lyxofuranosyl)-1,2,3-osotriazole 
• 74134-91-1 4-(β-D-lyxofuranosyl)-2-phenyl-1,2,3-osotriazole 
• 78548-27-3 2-phenyl-4-(2,3,5-tri-O-acetyl-β-D-arabinofuranosyl)-1,2,3-osotriazole 
• 74134-93-3 4-β-D-arabinofuranosyl-2-phenyl-1,2,3-osotriazole 

Relevant articles and documents

Studies on Anhydro-osazones. Part 5. Structure and Anomeric Configuration of the C-Nucleoside Analogues Obtained from the Dehydration of D-gluco- and D-manno-Hept-2-ulose Phenylosazones

Dehydration of D-gluco- and D-manno-hept-2-ulose phenylosazones with methanolic sulphuric acid afforded the anomeric furanosyl anhydro-osazone pair: 3,6-anhydro-D-manno-hept-2-ulose phenylosazone (2) and the gluco-analogue osazone (3).A new type of anomeric pyranosyl anhydro-osazone was also idenified.Refluxing the anhydro-osazones with copper sulphate afforded the anomeric furanosyl C-nucleoside analogues 4-α-D-arabinofuranosyl-2-phenyl-v-triazole (6) and the β-isomer (7), and the arabinofuranosyl isomers (8) and (9).The structures and anomeric configurations of the products were determined by periodate oxidation, o.r.d., and n.m.r. spectroscopy.The mechanism of the dehydration and the mass spectra of compounds (6)-(9) are discussed.

Studies on 3,6-anhydro-osazones of higher monosaccharides: characterization and anomeric configuration

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2-phenyl-1,2,3-osotriazole C-nucleoside analogs synthesis and determination of anomeric configuration

A series of anomeric 2-phenyl-1,2,3-osotriazole C-nucleoside analogs has been prepared. The anomeric configuration was determined by a novel method from the chemical shift of the C-5 proton of the osotriazole base moieties.