136034-23-6

Basic information

• Product Name: β-D-Glucopyranosylphenylmethane
• Synonyms: β-D-Glucopyranosylphenylmethane
• CAS NO: 136034-23-6
• Molecular Weight: 254.283
• Mol File: 136034-23-6.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: β-D-Glucopyranosylphenylmethane(CAS DataBase Reference)
• NIST Chemistry Reference: β-D-Glucopyranosylphenylmethane(136034-23-6)
• EPA Substance Registry System: β-D-Glucopyranosylphenylmethane(136034-23-6)

Safety Data

• Hazardous Substances Data: 136034-23-6(Hazardous Substances Data)

Upstream product

• 4291-69-4 2,3,4,6-Tetra-O-benzyl-D-glucopyranose 
• 13096-62-3 (3R,4S,5R,6R)-3,4,5-tris(benzyloxy)-6-((benzyloxy)methyl)tetrahydro-2H-pyran-2-one 
• 100-44-7 benzyl chloride 
• 100-52-7 benzaldehyde 
• 136034-18-9 (S)-[(4S,5R,6R)-3-((S)-Benzenesulfinyl)-4,5-bis-benzyloxy-6-benzyloxymethyl-5,6-dihydro-4H-pyran-2-yl]-phenyl-methanol 
• 136034-19-0 (2S,4S,4aS,6R,7R,8S,8aR)-7,8-Bis-benzyloxy-6-benzyloxymethyl-2,4-diphenyl-hexahydro-pyrano[3,2-d][1,3]dioxine 
• 136034-22-5 2,6-anhydro-3,4,5,7-tetra-O-benzyl-(1S)-C-phenyl-D-erythro-L-guloheptitol 
• 105938-05-4 (S)-((4R,5S,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-5,6-dihydro-4H-pyran-2-yl)-phenyl-methanol 
• 118916-46-4 (2R,3R,4S)-5-((S)-Benzenesulfinyl)-3,4-bis-benzyloxy-2-benzyloxymethyl-3,4-dihydro-2H-pyran 
• 54423-54-0 2,3,4,6-Tetra-O-benzyl 1-O-p-nitrobenzoyl D-glucopyranoside 
• 1589-82-8 phenylmagnesium bromide 
• 59531-24-7 2,3,4,6-tetra-O-benzyl-D-glucopyranoside 
• 4196-35-4 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl bromide 
• 67773-43-7 2,3,4,6-tetra-O-benzyl-α/β-D-glucopyranosyl bromide 

Downstream Products

• 136034-24-7 (2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)phenylmethane 
• 511274-48-9 (2R,4aR,6S,7R,8R,8aS)-6-Benzyl-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine-7,8-diol 
• 511274-42-3 (2R,4aR,6S,7S,8R,8aR)-6-Benzyl-7,8-dimethoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine 
• 511274-43-4 (2R,3R,4S,5S,6S)-6-Benzyl-2-hydroxymethyl-4,5-dimethoxy-tetrahydro-pyran-3-ol 
• 511274-74-1 Pent-4-enoic acid (2R,3R,4R,5S,6S)-6-benzyl-4,5-dimethoxy-2-pent-4-enoyloxymethyl-tetrahydro-pyran-3-yl ester 
• 511274-76-3 Undec-10-enoic acid (2R,3R,4R,5S,6S)-6-benzyl-4,5-dimethoxy-2-undec-10-enoyloxymethyl-tetrahydro-pyran-3-yl ester 
• 161909-26-8 (2,3,4,6-Tetra-O-acetyl-β-D-glucopyranosyl)-4-aminophenylmethane 
• 158419-85-3 (Methyl 2,3,4-tri-O-acetyl-β-D-glucopyranosyluronate)-4-retinamidophenylmethane 

Relevant articles and documents

Synthesis and screening of bicyclic carbohydrate-based compounds: A novel type of antivirals

A small library of bicyclic carbohydrate derivatives was synthesized and screened. A strong and selective activity against cytomegalovirus was found. Structure-activity relationship for this new type of antivirals is discussed.

Bicyclic carbohydrate compounds useful in the treatment of infections caused by herpesviridae

Bicyclic carbohydrates for the treatment of infections caused by herpseviridae, and in particular cytomegalovirus. The invention consists of the novel bicyclic carbohydrates the generic structure of which is: wherein R1 is either -Bn or -Ph; R2 and R3 are either -alkyl, -aryl, -allyl, or —H; R4 and R5 form a ring and are either —CH(Ph)- or —CH(aryl)- and X is either O, N or S.

Suzuki cross-coupling of carbohydrates: Synthesis of β-arylmethyl-C-glycosides and aryl-scaffolded trisaccharide mimics

β-1-C-Arylmethylglycoside derivatives of D-glucose and D-mannose have been synthesized using a mild hydroboration/Suzuki cross-coupling sequence. The scope and limitations of this methodology as well as its extension to the construction of aryl scaffolded trisaccharide mimics is described.