99749-54-9

Basic information

• Product Name: ALPHA-D(+)MANNOSE 1-PHOSPHATE SODIUM SALT
• Synonyms: ALPHA-D(+)MANNOSE 1-PHOSPHATE SODIUM SALT;ALPHA-D-MANNOPYRANOSYL PHOSPHATE SODIUM SALT;A-D(+)MANNOSE 1-PHOSPHATE SODIUM SIGMA*G RADE;α-d(+)mannose 1-phosphate sodium salt hydrate;a-D-Mannose-1-phosphatesodiumsalt;α-D-Mannose-1-phosphate sodium salt ,98%;α-D-Mannose phosphate sodium salt
• CAS NO: 99749-54-9
• Molecular Formula: C₆H₁₁O₉P*2Na
• Molecular Weight: 282.12
• Mol File: 99749-54-9.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• Storage Temp.: −20°C
• CAS DataBase Reference: ALPHA-D(+)MANNOSE 1-PHOSPHATE SODIUM SALT(CAS DataBase Reference)
• NIST Chemistry Reference: ALPHA-D(+)MANNOSE 1-PHOSPHATE SODIUM SALT(99749-54-9)
• EPA Substance Registry System: ALPHA-D(+)MANNOSE 1-PHOSPHATE SODIUM SALT(99749-54-9)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 99749-54-9(Hazardous Substances Data)

Usage

Chemical Properties

Solid

Upstream product

• 374726-35-9 dibenzyl 2,3,4,6-tetra-O-acetyl-D-glucopyranosyl phosphate 
• 149717-36-2 dibenzyl 2,3,4,6-tetra-O-acetyl-D-glucopyranosyl phosphite 
• 3947-62-4 2,3,4,5-tetra-O-acetyl-D-glucopyranose 
• 83-87-4 D-glucose pentaacetate 

Relevant articles and documents

Synthesis and use of glycosyl phosphites: An effective route to glycosyl phosphates, sugar nucleotides, and glycosides

An efficient and convenient synthetic route to glycosyl phosphites and phosphates has been developed that uses dibenzyl N,N-diethylphosphoramidite as a phosphitylating reagent. Glycosyl phosphites and phosphates of 2-acetamido-2-deoxy-D-galactose (GalNAc) (29), 2-acetamido-2-deoxy-D-glucose (GlcNAc) (30), D-galactose (Gal) (31), D-glucose (Glc) (32), D-mannose (Man) (33), L-rhamnose (Rha) (34), L-fucose (Fuc) (35), and N-acetylneuraminic acid (NeuAc) (41) were prepared by this procedure. Compounds 29 and 30 were obtained as α anomers exclusively, whereas compounds 31, 32, and 41 were obtained as β anomers, and compounds 33 and 34, as α anomers, predominately. The phosphates are useful for the synthesis of sugar nucleotides, and the phosphites are effective glycosylation reagents.