74895-01-5

Upstream product

• 1125-88-8 benzaldehyde dimethyl acetal 
• 7216-73-1 methyl β-D-cellobioside 
• 100-52-7 benzaldehyde 

Downstream Products

• 84094-20-2 methyl 4-O-(4,6-O-benzylidene-β-D-allopyranosyl)-β-D-allopyranoside 
• 84094-19-9 methyl 2,3,6-tri-O-acetyl-4-O-(2,3-di-O-acetyl-4,6-O-benzylidene-β-D-allopyranosyl)-β-D-allopyranoside 
• 84094-18-8 methyl 2,6-di-O-benzoyl-4-O-<3-O-benzoyl-4,6-O-benzylidene-2-O-(methylsulfonyl)-β-D-allopyranosyl>-2-O-(methylsulfonyl)-β-D-allopyranoside 
• 84093-87-8 methyl 2,3-di-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-6-O-p-tolylsulfonyl-β-D-glucopyranoside 
• 84093-86-7 methyl 2,3-di-O-acetyl-4-O-(2,3-di-O-acetyl-4,6-O-benzylidene-β-D-glucopyranosyl)-6-O-p-tolylsulfonyl-β-D-glucopyranoside 
• 84094-25-7 methyl 4-O-<4,6-O-benzylidene-2,3-di-O-(methylsulfonyl)-β-D-glucopyranosyl>-6-deoxy-2,3-di-O-(methylsulfonyl)-β-D-glucopyranoside 
• 84094-22-4 methyl 2,3-di-O-acetyl-6-deoxy-4-O-(2,3-di-O-acetyl-4,6-O-benzylidene-β-D-glucopyranosyl)-6-iodo-β-D-glucopyranoside 
• 84094-23-5 methyl 2,3-di-O-acetyl-6-deoxy-4-O-(2,3-di-O-acetyl-4,6-O-benzylidene-β-D-glucopyranosyl)-β-D-glucopyranoside 
• 84094-24-6 methyl 4-O-(4,6-O-benzylidene-β-D-glucopyranosyl)-6-deoxy-β-D-glucopyranoside 
• 84094-26-8 methyl 4-O-(4,6-O-benzylidene-2,3-dideoxy-β-D-erythro-hex-2-enopyranosyl)-2,3,6-trideoxy-β-D-erythro-hex-2-enopyranoside 
• 84094-29-1 Benzoic acid (2S,3S,6R)-2-bromomethyl-6-((2R,3S,6R)-6-methoxy-2-methyl-tetrahydro-pyran-3-yloxy)-tetrahydro-pyran-3-yl ester 
• 84094-27-9 methyl 4-O-(4,6-O-benzylidene-2,3-dideoxy-β-D-erythro-hexopyranosyl)-2,3,6-trideoxy-β-D-erythro-hexopyranoside 
• 84094-28-0 methyl 4-O-(4-O-benzoyl-2,3,6-trideoxy-β-D-erythro-hexopyranosyl)-2,3,6-trideoxy-β-D-erythro-hexopyranoside 
• 84093-84-5 methyl 4-O-(4,6-O-benzylidene-2,3-di-O-methyl-β-D-glucopyranosyl)-2,3,6-tri-O-methyl-β-D-glucopyranoside 

Relevant academic research and scientific papers

CHEMICAL MODIFICATION OF METHYL β-CELLOBIOSIDE

Treatment of methyl β-cellobioside (1) with α,α-dimethoxytoluene in N,N-dimethylformamide in the presence of p-toluenesulfonic acid gave a high yield of methyl 4',6'-O-benzylidene-β-cellobioside (6), which was transformed into methyl 2,3,2',3',4',6'-hexa-

Trityl Derivatives of Cellobiose. VI. Unambiguous Assignments of Acetoxyl Group Resonances in the 1H-NMR Spectra of 6,6'-Di-O-trityl-, 6-O-Trityl-, and 6'-O-Tritylcellobiose Peracetates

The 1H-NMR spectra of 6,6'-di-O-trityl-, 6-O-trityl-, and 6'-O-tritylcellobiose peracetates (I-1, II-1, and III-1) showed some of the acetoxyl group resonances at abnormally high fields in CDCl3 and all their acetoxyl group signals were resolved in the re