84447-05-2

Basic information

• Product Name: 2,5-anhydro-1,6-di-O-tosyl-D-mannitol
• Synonyms: 2,5-anhydro-1,6-di-O-tosyl-D-mannitol
• CAS NO: 84447-05-2
• Molecular Weight: 472.537
• Mol File: 84447-05-2.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2,5-anhydro-1,6-di-O-tosyl-D-mannitol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-anhydro-1,6-di-O-tosyl-D-mannitol(84447-05-2)
• EPA Substance Registry System: 2,5-anhydro-1,6-di-O-tosyl-D-mannitol(84447-05-2)

Safety Data

• Hazardous Substances Data: 84447-05-2(Hazardous Substances Data)

Upstream product

• 22144-41-8 2,5-anhydro-1,6-di-O-benzoyl-D-glucitol 
• 98-59-9 p-toluenesulfonyl chloride 
• 27826-73-9 2,5-anhydro-D-glucitol 
• 495-75-0 2,5-anhydro-D-mannose 
• 41107-82-8 2,5-anhydro-D-mannitol 
• 65729-86-4 1,3,4,6-tetra-O-acetyl-2,5-anhydro-D-glucitol 

Downstream Products

• 22474-44-8 2,5:3,6-dianhydro-1-deoxy-4-O-p-tolylsulfonyl-D-glucitol 
• 84447-06-3 3,4-di-O-acetyl-2,5-anhydro-1,6-di-O-(p-tolylsulfonyl)-D-mannitol 
• 88777-14-4 2,5:3,6-dianhydro-1-O-p-tolylsulfonyl-D-glucitol 
• 84447-06-3 3,4-di-O-acetyl-2,5-anhydro-1,6-di-O-p-tolylsulfonyl-D-glucitol 

Relevant articles and documents

Chiral diphosphorus compounds and their transition metal complexes

The present invention relates to chiral diphosphorus compounds and their transition metal complexes, to a process for preparing chiral diphosphorus compounds and their transition metal complexes and also to their use in asymmetric syntheses.

Synthesis of rigid, chiral 1,5-diamino-3-oxapentanes and incorporation into chiral macrocyclic polyether ligands

The synthesis of 2,5-anhydro-1,6-di-C-amino-1,6-dideoxy-3,4-di-O-methyl-D-mannitol 11 and its N,N'-dimethyl analogue 15 are described, as are couplings to bis-tartaro-18-crown-6 1 to give a macrobicyclic cryptand 16, and macrocycles 17 and 18 bearing four lateral groups, which are potential precursors of a cylindrical stacked macrocyclic system such as 6.

SYNTHESIS OF "DOUBLE-HEADED" BIS-HOMONUCLEOSIDE ANALOGS

The synthesis of "double-headed" bis-homonucleoside analogs, containing an oxolane ring with D-arabo and L-lyxo configuration is described.As starting material differently substituted 1,6-diazido-1,6-dideoxy-2,5-anhydro-D-glucitol and L-iditol derivatives