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

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

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

Downstream Products

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

Chiral diphosphorus compounds and transition metal complexes thereof

Tetrahydrofuran bisphosphines of formula (I), are new. Tetrahydrofuran bisphosphines of formula (I): X1, X2 = bonds or O; R1, R2 = H, 1-20C alkyl, 1-20C fluoroalkyl, 2-20C alkenyl, 4-24C aryl, 5-25C aralkyl, 6-26C aralkenyl, NR7R8, OR8, AOR8, ANR7R8 or OC

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 6-AMINO-2,5-ANHYDRO-6-DEOXY-AND -1,6-DIDEOXY-D-GLUCITOL AND SOME DERIVATIVES THEREOF

6-Amino-2,5-anhydro-6-deoxy- and -1,6-dideoxy-D-glucitol (44), as well as some of their derivatives, were synthesized, starting from D-mannitol. 3,4-Di-O-allyl-1,2:5,6-dianhydro-D-mannitol was converted into the 2,5-anhydro-6-bromo compound 8, the bromine

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