29780-95-8

Basic information

• Product Name: 1,6-di-O-trityl-D-glucitol
• Synonyms: 1,6-di-O-trityl-D-glucitol
• CAS NO: 29780-95-8
• Molecular Weight: 666.814
• Mol File: 29780-95-8.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1,6-di-O-trityl-D-glucitol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,6-di-O-trityl-D-glucitol(29780-95-8)
• EPA Substance Registry System: 1,6-di-O-trityl-D-glucitol(29780-95-8)

Safety Data

• Hazardous Substances Data: 29780-95-8(Hazardous Substances Data)

Upstream product

• 50-70-4 D-sorbitol 
• 76-83-5 trityl chloride 
• 110-86-1 pyridine 

Downstream Products

• 1607827-97-3 (1R,2S,3R,4R,5R,6R)-3,4,5,6-tetrakis(benzyloxy)cyclohexane-1,2-diol 
• 1607827-91-7 (2S,3S,4S,5R,6R)-6-acetoxy-2,3,4,5-tetrakis(benzyloxy)-cyclohexanone 
• 1607827-90-6 (2S,3S,4R,5S,6R)-2,3,4,5-tetrakis(benzyloxy)-6-hydroxycyclohexanone 
• 1607827-85-9 (2S,3S,4S,5S,6R)-6-acetoxy-2,3,4,5-tetrakis(benzyloxy)-cyclohexanone 
• 1607827-84-8 (2S,3S,4R,5R,6R)-2,3,4,5-tetrakis(benzyloxy)-6-hydroxycyclohexanone 
• 1023310-53-3 2,3,4,5-tetra-O-benzyl-1,6-di-O-trityl-D-glucitol 
• 4261-26-1 O²,O³,O⁴,O⁵-tetramethyl-D-glucose 
• 256342-72-0 2,3,4,5-tetrakis-benzyloxyhexane-1,6-diol 
• 195873-70-2 (3R,4R,5R,6S)-3,4,5,6-tetra(benzoyloxy)-1,7-octadiene 
• 277744-76-0 2,3,4,5-tetra-O-benzyl-D-gluco-hexodialdose 
• 224433-58-3 (3R,4R,5R,6S)-3,4,5,6-tetra(benzyloxy)-cyclohexene 
• 161754-57-0 2,3,4,5-tetra-O-methyl-1,6-di-O-trityl-D-glucitol 
• 29780-96-9 1.6-Ditrityl-D-glucit-2.3.4.5-tetrastearinsaeureester 

Relevant articles and documents

A straightforward synthesis of perbenzylated conduritols from alditols by ring closing olefin metathesis

The synthesis of perbenzylated conduritols A, E and F has been achieved in six steps by formal conversion of galactitol, D-mannitol and D-glucitol into the respective terminal dienes, followed by ring closing olefin metathesis. The Royal Society of Chemistry 1999.

Improved stereochemical analysis of conformationally flexible diamines by binding to a bisporphyrin molecular clip

The relative stereochemistry of acyclic diamines with several stereogenic centers has been analyzed by NMR spectroscopy in combination with conformational deconvolution. Binding to a bisporphyrin molecular clip improves the stereochemical assignment signi

Asymmetric synthesis using reactions with modest group selectivity

The isomeric purity of products from certain group-selective reactions can be significantly amplified when reactions can occur sequentially.The theoretical basis for a strategy that exploits reactions with modest enantiotopic group selectivity for asymmet