37614-73-6

Basic information

• Product Name: 1,2-O-isopropylidene-α-D-glucofuranose 3-O-benzoate
• Synonyms: 1,2-O-isopropylidene-α-D-glucofuranose 3-O-benzoate
• CAS NO: 37614-73-6
• Molecular Weight: 324.331
• Mol File: 37614-73-6.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: 1,2-O-isopropylidene-α-D-glucofuranose 3-O-benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-O-isopropylidene-α-D-glucofuranose 3-O-benzoate(37614-73-6)
• EPA Substance Registry System: 1,2-O-isopropylidene-α-D-glucofuranose 3-O-benzoate(37614-73-6)

Safety Data

• Hazardous Substances Data: 37614-73-6(Hazardous Substances Data)

Upstream product

• 286011-06-1 1,2:5,6-di-O-isopropylidene-α-D-galactofuranose 
• 582-52-5 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 98-88-4 benzoyl chloride 
• 4105-61-7 3-O-Benzyl-5,6-didehydro-5,6-dideoxy-1,2-isopropyliden-α-D-xylo-hexofuranose 
• 3254-32-8 6-O-benzoyl-1,2-O-isopropylidene-α-D-glucofuranose 
• 182412-45-9 Benzoic acid (3aR,5R,6S,6aR)-2,2-dimethyl-5-((R)-2-thioxo-[1,3]dioxolan-4-yl)-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl ester 
• 81712-62-1 Benzoic acid (3aR,5R,6S,6aR)-5-((R)-1,2-bis-benzhydryloxy-ethyl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl ester 
• 13964-22-2 3-O-benzoyl-1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 

Downstream Products

• 55263-77-9 O³,O⁶-dibenzoyl-O¹,O²-isopropylidene-O⁵-(toluene-4-sulfonyl)-α-D-glucofuranose 
• 81058-34-6 6-Azido-3-O-benzoyl-6-desoxy-1,2-O-isopropyliden-4-O-(methylsulfonyl)-α-D-glucopyranose 
• 81058-60-8 6-Azido-6-desoxy-1,2-O-isopropyliden-4-O-(p-tolylsulfonyl)-α-D-glucopyranose 
• 81058-59-5 6-Azido-6-desoxy-1,2-O-isopropyliden-3-O-(p-tolylsulfonyl)-α-D-glucopyranose 
• 81058-33-5 6-Azido-3-O-benzoyl-6-desoxy-1,2-O-isopropyliden-α-D-glucopyranose 
• 81058-32-4 6-Azido-3-O-benzoyl-6-desoxy-1,2-O-isopropyliden-α-D-glucofuranose 
• 4105-61-7 3-O-Benzyl-5,6-didehydro-5,6-dideoxy-1,2-isopropyliden-α-D-xylo-hexofuranose 
• 55169-76-1 3,6-di-O-benzoyl-1,2-O-isopropylidene-α-D-glucofuranose 
• 3254-32-8 6-O-benzoyl-1,2-O-isopropylidene-α-D-glucofuranose 
• 81712-62-1 Benzoic acid (3aR,5R,6S,6aR)-5-((R)-1,2-bis-benzhydryloxy-ethyl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl ester 
• 983-79-9 benzophenone azine 
• 81058-31-3 3-O-benzoyl-1,2-O-isopropylidene-6-O-p-toluenesulfonyl-α-D-glucofuranose 
• 66954-56-1 O⁵,O⁶-diacetyl-O³-benzoyl-O¹,O²-isopropylidene-α-D-glucofuranose 

Relevant articles and documents

Thioglucose compound and preparation method thereof

The invention provides a thioglucose compound which has the following general formula: Wherein R is selected from H or acetyl. The preparation method of the thioglucose compound is easy to obtain, low in production cost and suitable for industrial product

Catalytic asymmetric dihydroxylation of olefins using polysulfone-based novel microencapsulated osmium tetroxide

A polysulfone based novel polymer-supported osmium catalyst has been developed. The catalyst was prepared from commercially available polysulfone, based on a microencapsulation technique and was employed in the asymmetric dihydroxylation of various olefins using (DHQD)2PHAL as the chiral ligand and NMO as the co-oxidant in H2O-acetone-CH3CN (1:1:1). The catalyst was recovered by simple filtration and was reused to obtain excellent yields with good enantioselectivity up to five times.

Sulfuric acid immobilized on silica: an efficient reusable catalyst for selective hydrolysis of the terminal O-isopropylidene group of sugar derivatives

Sulfuric acid immobilized on silica proved to be an efficient catalyst for selective hydrolysis of the terminal O-isopropylidene group of sugar derivatives. The method is very simple and economic for large-scale synthesis in which the catalyst is recovered and reused for several runs. Reactions with di-O-isopropylidene derivatives of d-glucose, d-mannose, d-fructose and l-sorbose led to the formation of the corresponding mono-O-isopropylidene derivatives in good to excellent yields.