88877-45-6

Basic information

• Product Name: C₃₀H₅₀N₂O₉⁽²⁺⁾*2I^(1-)
• CAS NO: 88877-45-6
• Molecular Weight: 836.544
• Mol File: 88877-45-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: C₃₀H₅₀N₂O₉⁽²⁺⁾*2I^(1-)(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₀H₅₀N₂O₉⁽²⁺⁾*2I^(1-)(88877-45-6)
• EPA Substance Registry System: C₃₀H₅₀N₂O₉⁽²⁺⁾*2I^(1-)(88877-45-6)

Safety Data

• Hazardous Substances Data: 88877-45-6(Hazardous Substances Data)

Upstream product

• 95120-38-0 methyl 4,6-O-benzylidene-2,3-O-bis(p-toluenesulphonyloxyethyl)-α-D-galactopyranoside 
• 130787-46-1 methyl 4,6-O-benzylidene-2,3-bis(2-iodoethoxy)-α-D-galactoside 
• 58688-38-3 7,13-dimethyl-7,13-diaza-1,4,10-trioxacyclopentadecane 
• 34270-90-1 2,2'-diiodoethyl ether 
• 88877-44-5 (4aR,6S,6aR,22aS,22bS)-6-Methoxy-10,19-dimethyl-2-phenyl-hexadecahydro-1,3,5,7,13,16,22-heptaoxa-10,19-diaza-cyclooctadeca[a]naphthalene 
• 95120-37-9 methyl 4,6-O-benzylidene-2,3-O-bis(p-toluenesulphonyloxyethyl)-α-D-glucopyranoside 
• 130787-45-0 methyl 4,6-O-benzylidene-2,3-bis(2-iodoethoxy)-α-D-glucoside 
• 88877-43-4 (4aR,6S,6aR,22aS,22bR)-6-Methoxy-10,19-dimethyl-2-phenyl-hexadecahydro-1,3,5,7,13,16,22-heptaoxa-10,19-diaza-cyclooctadeca[a]naphthalene 
• 86534-17-0 methyl 4,6-O-benzylidene-2,3-O-bis(p-toluenesulphonyloxyethyl)-α-D-mannopyranoside 
• 130787-47-2 methyl 4,6-O-benzylidene-2,3-bis(2-iodoethoxy)-α-D-mannoside 
• 86534-19-2 (4aR,6S,6aS,22aS,22bR)-6-Methoxy-10,19-dimethyl-2-phenyl-hexadecahydro-1,3,5,7,13,16,22-heptaoxa-10,19-diaza-cyclooctadeca[a]naphthalene 

Downstream Products

• 88877-49-0 C₂₈H₄₄N₂O₉ 
• 88877-50-3 C₂₈H₄₄N₂O₉ 
• 88877-48-9 C₂₈H₄₄N₂O₉ 

Relevant articles and documents

A New Strategy for the High-Pressure Synthesis of Chiral Cryptands

A new strategy for the high-pressure synthesis of chiral cryptands is reported.Four chiral cryptands derived fro D-glucose, D-galactose, D-mannose and L-tartaric acid are prepared in a short reaction sequence.

High-pressure Approach to the Synthesis of Novel Chiral Cryptands Derived from Methyl 4,6-O-Benzylidene-α-D-manno-, -α-D-galacto-, and -α-D-gluco-pyranoside

Diaza crown ethers derived from sugars react under high pressure with bis-(2-iodoethyl) ether to give the quaternary salts in quantitative yield and their subsequent demethylation with triphenylphosphine affords chiral cryptands in high yield.