75810-07-0

Basic information

• Product Name: Benzyl 2,6-Dideoxy-α-D-arabino-hexopyranoside
• Synonyms: Benzyl 2,6-Dideoxy-α-D-arabino-hexopyranoside
• CAS NO: 75810-07-0
• Molecular Weight: 238.284
• Mol File: 75810-07-0.mol

Chemical Properties

• CAS DataBase Reference: Benzyl 2,6-Dideoxy-α-D-arabino-hexopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: Benzyl 2,6-Dideoxy-α-D-arabino-hexopyranoside(75810-07-0)
• EPA Substance Registry System: Benzyl 2,6-Dideoxy-α-D-arabino-hexopyranoside(75810-07-0)

Safety Data

• Hazardous Substances Data: 75810-07-0(Hazardous Substances Data)

Upstream product

• 90762-86-0 Acetic acid (2R,3R,4R)-3-acetoxy-6-benzyloxy-2-methyl-tetrahydro-pyran-4-yl ester 
• 75124-36-6 Benzyl-4-O-benzyl-2,6-didesoxy-6-iod-α-D-arabino-hexopyranosid 
• 474017-59-9 benzyl 3,4-di-O-acetyl-2-bromo-2,6-dideoxy-α-D-mannopyranoside 
• 61-58-5 2-deoxy-D-arabino-hexopyranose 
• 50615-76-4 benzyl 2-deoxy-α-D-arabino-hexopyranoside 
• 100-51-6 benzyl alcohol 
• 89063-61-6 1,3,4-Tri-O-acetyl-2,6-didesoxy-D-arabino-hexopyranose 
• 92611-21-7 benzyl 3,4-di-O-acetyl-2,6-dibromo-2,6-dideoxy-α-D-glucopyranoside 
• 92611-14-8 benzyl 3,4-di-O-acetyl-2,6-dibromo-2,6-dideoxy-α-D-mannopyranoside 
• 76739-66-7 3,4-di-O-acetyl-D-rhamnal 
• 145295-38-1 benzyl 6-bromo-2,6-dideoxy-α-D-glucopyranoside 
• 90762-86-0 benzyl 3,4-di-O-acetyl-2,6-dideoxy-α-D-glucopyranoside 
• 78185-01-0 2,6-dideoxy-α-D-arabino-hexopyranose 
• 78138-31-5 3,4-di-O-acetyl-2,6-dibromo-2,6-dideoxy-α-D-glucopyranosyl bromide 

Downstream Products

• 90762-88-2 Benzyl 3-O-Benzyl-2,6-dideoxy-α-D-arabino-hexopyranoside 
• 75124-38-8 Benzyl 4-O-Benzyl-2,6-dideoxy-α-D-arabino-hexopyranoside 
• 90762-89-3 (2R,3R,4R,6S)-3,4,6-Tris-benzyloxy-2-methyl-tetrahydro-pyran 
• 474017-73-7 benzyl 3-O-(tert-butyldimethylsilyl)-2,6-dideoxy-α-D-glucopyranoside 
• 474017-85-1 benzyl 3,4-anhydro-2,6-dideoxy-α-D-galactopyranoside 
• 474018-04-7 benzyl 3,4-anhydro-2,6-dideoxy-α-D-allopyranoside 
• 90763-05-6 Benzyl 4-O-(3,4-Di-O-acetyl-2,6-dibromo-2,6-dideoxy-α-D-glucopyranosyl)-3-O-benzyl-2,6-dideoxy-α-D-arabino-hexopyranoside 
• 90763-06-7 Benzyl 4-O-(3,4-Di-O-acetyl-2,6-dibromo-2,6-dideoxy-β-D-glucopyranosyl)-3-O-benzyl-2,6-dideoxy-α-D-arabino-hexopyranoside 
• 90762-92-8 Benzyl 4-O-(3,4-Di-O-acetyl-2,6-dibromo-2,6-dideoxy-α-D-mannopyranosyl)-3-O-benzyl-2,6-dideoxy-α-D-arabino-hexopyranoside 
• 90762-96-2 Benzyl 4-O-(3,4-Di-O-acetyl-2,6-dideoxy-α-D-arabino-hexopyranosyl)-3-O-benzyl-2,6-dideoxy-α-D-arabino-hexopyranoside 
• 90763-08-9 Benzyl-4-O-(3,4-di-O-acetyl-2,6-didesoxy-β-D-arabino-hexopyranosyl)-2,6-didesoxy-3-O-benzyl-α-D-arabino-hexopyranosid 
• 474017-77-1 (+)-benzyl 3-(O-t-butyldimethylsilyl)-4-(O-mesyl)-2,6-dideoxy-α-D-glucopyranoside 
• 474017-81-7 benzyl 4-O-mesyl-2,6-dideoxy-α-D-glucopyranoside 

Relevant articles and documents

Regiochemical control of the ring opening of 1,2-epoxides by means of chelating processes. Part 17: Synthesis and opening reactions of cis- and trans-oxides derived from (2S,6R)-2-benzyloxy-6-methyl-3,6-dihydro-2H-pyran, (2R,6R)- and (2S,6R)-2-methoxy-6-m

The regiochemical behavior of the title deoxy anhydrosugars, prepared in an enantioselective way starting from methyl α-D-glucopyranoside, was examined in opening reactions, both under standard and chelating conditions. The results clearly indicate the in

Unusual stereoselectivity in sialic acid aldolase-catalyzed aldol condensations: Synthesis of both enantiomers of high-carbon monosaccharides

An inversion of stereoselectivity in aldol condensations catalyzed by sialic acid aldolase (from Escherichia coli, Shinko American Inc.) was observed when L-mannose, 6-deoxy-L-mannose, L-talose, 2-deoxy-L-glucose, 2-deoxy-L-rhamnose, N-acetyl-L-mannosamin

Preparation of α- and β-Linked Disaccharides of 2,6-Dideoxy-D-arabino-hexose. Synthesis of Bamflalactone

1,4-α-Linked disaccharides of 2,6-dideoxy-D-arabino-hexose are prepared from the selectively protected 2,6-dideoxy sugars 3 or 4 and the 1,5-anhydrohex-1-enitol (9) by using the N-iodosuccinimide (NIS) method or from the deoxy sugar 6 and the acetylated 2

2-BROMO-2-DEOXY SUGARS AS STARTING MATERIALS FOR THE SYNTHESIS OF α- OR β-GLYCOSIDES OF 2-DEOXY SUGARS

3,4-Di-O-acetyl-2,6-dibromo-2,6-dideoxy-α-D-gluco- (1) and -D-mannopyranosyl bromide (18) gave, in glycosidation reactions, 1,2-trans-glycosides. β-D-Glycosides were formed as the main products from 1 in moderate yields, whereas 18 gave α-D-glycosides exc