20706-90-5

Basic information

• Product Name: 2-amino-2-deoxy-α-D-talopyranose; hydrochloride
• Synonyms: 2-amino-2-deoxy-α-D-talopyranose; hydrochloride
• CAS NO: 20706-90-5
• Molecular Weight: 215.634
• Mol File: 20706-90-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-amino-2-deoxy-α-D-talopyranose; hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: 2-amino-2-deoxy-α-D-talopyranose; hydrochloride(20706-90-5)
• EPA Substance Registry System: 2-amino-2-deoxy-α-D-talopyranose; hydrochloride(20706-90-5)

Safety Data

• Hazardous Substances Data: 20706-90-5(Hazardous Substances Data)

Upstream product

• 87-81-0 D-tagatose 
• 41847-61-4 (3S,4S,5R)-2-(hydroxymethyl)tetrahydropyran-2,3,4,5-tetrol 
• 887472-18-6 N-benzyl-D-tagatosylamine 
• 103782-08-7 allosamidin 

Downstream Products

• 66395-17-3 1-methyl-1-nitroso-3-(2-deoxy-D-galactos-2-yl)urea 
• 51471-40-0 2-Amino-N-anisyliden-2-deoxy-L-glucose 
• 3006-58-4 2-carbobenzyloxyamino-2-deoxy-D-galactopyranose 
• 20183-89-5 (3aR)-3-(3,4-dichloro-phenyl)-5t-((R)-1,2-dihydroxy-ethyl)-6t-hydroxy-(3ar,6ac)-hexahydro-furo[2,3-d]imidazole-2-thione 
• 31505-45-0 2-((3R,4R,5R,6R)-2,4,5-Trihydroxy-6-hydroxymethyl-tetrahydro-pyran-3-yl)-isoindole-1,3-dione 
• 149038-33-5 (4S,5S)-4-(D-arabino-tetritol-1-yl)-1-(4-chlorophenyl)-5-hydroxyimidazolidin-2-one 
• 98-98-6 2-Picolinic acid 
• 16932-62-0 D-mannosaminic acid 
• 81176-80-9 D-galactosaminic acid 
• 3006-60-8 2-acetamido-1,3,4,6-tetra-O-acetyl-2-deoxy-β-D-galactopyranose 
• 882503-87-9 2-[(E)-cinnamylidene]amino-2-deoxy-D-galactopyranose 
• 1355005-40-1 (3R,4R,5R,6R)-6-(acetoxymethyl)-3-aminotetrahydro-2H-pyran-2,4,5-triyl triacetate hydrochloride 
• 100483-05-4 2-deoxy-2-[[(phenylmethoxy)carbonyl]amino]-D-galactopyranose-1,3,4,6-tetraacetate 
• 1360862-26-5 C₅₇H₅₆Cl₃NO₁₂S 

Relevant articles and documents

Synthesis of N-protected galactosamine building blocks from D-tagatose via the heyns rearrangement

N-Acetyl-D-galactosamine (11), a very important naturally occurring building block of oligosaccharides, is easily accessible via the Heyns rearrangement of D-tagatose (3) with benzylamine. The short and efficient synthesis of various differently N-protected D-galactosamine derivatives is reported. Copyright Taylor & Francis Group, LLC.

Synthesis of 2-amino-2-deoxyglycoses and 2-amino-2-deoxyglycosides from glycals

O-acetylated glycals react with ceric ammonium nitrate in the presence of sodium azide to provide, in good yield, O-acetylated 2-azido-2-deoxy glycosyl nitrates. These nitrates can be used to prepare 2-amino-2-deoxy sugars, such as D-galactosamine and lactosamine. The O-acetylated 2-azido-2-deoxy glycosyl nitrates can alternately be converted to O-acetylated 2-azido-2-deoxy glycosyl halides which are useful in the preparation of O-acetylated 2-azido-2-deoxy glycosides, which in turn can be reduced to 2-amino-2-deoxy glycosides. Of particular interest are the syntheses of 2-amino-2-deoxy glycosides which correspond to the terminal units of the antigenic determinant for the human A blood group. Attachment of these glycosides to a solid support provides immunoabsorbents which efficiently and preferentially absorb anti-A antibodies from blood plasma.