123672-56-0

Basic information

• Product Name: 3-deoxy-L-gulo-2-octulosonic acid
• CAS NO: 123672-56-0
• Molecular Weight: 238.194
• Mol File: 123672-56-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3-deoxy-L-gulo-2-octulosonic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3-deoxy-L-gulo-2-octulosonic acid(123672-56-0)
• EPA Substance Registry System: 3-deoxy-L-gulo-2-octulosonic acid(123672-56-0)

Safety Data

• Hazardous Substances Data: 123672-56-0(Hazardous Substances Data)

Upstream product

• 328-42-7 Oxalacetic acid 
• 609-06-3 L-xylose 
• 113409-52-2 3-deoxy-2,5,6,7,8-penta-O-acetyl-L-gulo-2-octenoic acid γ-lactone 
• 113443-91-7 2-hydroxy-3-deoxy-5,6,7,8-tetra-O-acetyl-L-gulo-2-octenoic acid γ-lactone 

Relevant articles and documents

Synthesis and immunoreactivity of poly(acrylamide) copolymers containing C-3- and C-7-modified, carboxyl-reduced, 4-O- and 5-O-phosphorylated Kdo residues

Sodium (allyl 3-deoxy-α-D-lyxo-2-heptulopyranosid)onate (6), allyl 3-deoxy-β- and -α-D-manno-2-octulopyranoside, sodium (allyl 3-deoxy-β-L-gulo-2-octulopyranosid)onate, sodium (allyl α-D-glycero-D-talo-2-octulopyranosid)onate, sodium (allyl α-D-glycero-D-galacto-2-octulopyranosidonate, ammonium (allyl 3-deoxy-4-O- and -5-O-phosphono-α-D-manno-2-octulopyranosid)onate, and ammonium (allyl 3-deoxy-4-O- and -5-O-phosphono-β-D-manno-2-octulopyranosid)onate were prepared and copolymerized with acrylamide to give multivalent haptens, which were used in immune inhibition assays. The monoclonal antibody A 20, directed against α-pyranoside Kdo residues, did not react with these compounds, except with heptulosonic acid derivative 6, thus proving that the terminal hydroxymethyl group of Kdo is not required for binding. Sodium (allyl 3-deoxy-α-D-(yxo-2-heptulopyranosid)onate (6), allyl 3-deoxy-β- and -α-D-manno-2-octulopyranoside, sodium (allyl 3-deoxy-β-L-gulo-2-octulopyranosid)onate, sodium (allyl α-D-glycero-D-talo-2-octulopyranosid)onate, sodium (allyl α-D-glycero-D-galacto-2-octolopyranosidonate, ammonium (allyl 3-deoxy-4-O- and -5-O-phosphono-α-D-manno-2-octulopyranosid)onate, and ammonium (allyl 3-deoxy-4-O- and -5-O-phosphono-β-D-manno-2-octulopyranosid)onate were prepared and copolymerized with acrylamide to give multivalent haptens, which were used in immune inhibition assays. The monoclonal antibody A 20, directed against α-pyranoside Kdo residues, did not react with these compounds, except with heptulosonic acid derivative 6, thus proving that the terminal hydroxymethyl group of Kdo is not required for binding.