79528-51-1

Basic information

• Product Name: Phenyl 4,6-O-benzylidene-2-deoxy-2-phthalimido-1-thio-beta-D-glucopyranoside
• Synonyms: Phenyl 4,6-O-benzylidene-2-deoxy-2-phthalimido-1-thio-beta-D-glucopyranoside
• CAS NO: 79528-51-1
• Molecular Weight: 489.549
• Mol File: 79528-51-1.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Phenyl 4,6-O-benzylidene-2-deoxy-2-phthalimido-1-thio-beta-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: Phenyl 4,6-O-benzylidene-2-deoxy-2-phthalimido-1-thio-beta-D-glucopyranoside(79528-51-1)
• EPA Substance Registry System: Phenyl 4,6-O-benzylidene-2-deoxy-2-phthalimido-1-thio-beta-D-glucopyranoside(79528-51-1)

Safety Data

• Hazardous Substances Data: 79528-51-1(Hazardous Substances Data)

Upstream product

• 31505-45-0 2-deoxy-2-phthalimido-D-glucopyranose 
• 85-44-9 phthalic anhydride 
• 79528-49-7 phenyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside 
• 17314-33-9 tributyltin phenyl sulfide 
• 4551-15-9 phenylthiotrimethylsilane 
• 10022-13-6 1,3,4,6-tetra-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranose 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 136882-36-5 2-((2S,3R,4R,5S,6R)-4,5-Dihydroxy-6-hydroxymethyl-2-phenylsulfanyl-tetrahydro-pyran-3-yl)-isoindole-1,3-dione 

Downstream Products

• 79528-53-3 phenyl 3-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside 
• 79528-54-4 phenyl 6-O-acetyl-3-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside 
• 79528-55-5 phenyl 6-O-benzoyl-3-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside 
• 148705-03-7 phenyl 4,6-benzylidene-2-deoxy-3-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside 
• 141342-83-8 phenyl 6-O-benzyl-2-deoxy-2-phthalimido-1-thio-1-deoxy-β-D-glucopyranoside 
• 79528-52-2 2-((4aR,6S,7R,8R,8aS)-8-Benzyloxy-2-phenyl-6-phenylsulfanyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl)-isoindole-1,3-dione 
• 141342-85-0 Phenyl O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->4)-O-<(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1->3)>-6-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside 
• 141342-84-9 Phenyl O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->4)-6-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside 
• 148705-05-9 4-nitrophenyl O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1-3)-O-(4,6-di-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-(1-3)-2,4,6-tri-O-acetyl-β-D-galactopyranoside 
• 148705-04-8 Acetic acid (2R,3S,4R,5R,6S)-2-acetoxymethyl-5-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-6-phenylsulfanyl-4-((2R,3R,4S,5S,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-3-yl ester 

Relevant articles and documents

BIFUNCTIONAL COMPOUND AND ITS USE IN IMMUNOTHERAPY

The invention relates to a bifunctional compound that is, on one side, an agonist of the TLR4 and, on the other side, an important inhibitor of the PSMA. Said compound is useful in immunotherapy for the treatment and/or prevention of prostate cancer. Therefore, the invention also relates to the use of the compound and to the pharmaceutical composition comprising it.

Iodine-catalyzed one-pot acetalation-esterification reaction for the preparation of orthogonally protected glycosides

An iodine-catalyzed one-pot tandem acetalation-esterification reaction of thio- and O-glycosides has been developed providing a fast and mild route to orthogonally protected glycosides ready to be used as building blocks in glycosylation reactions.

Synthesis of phenyl 6-O-acyl-3-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside

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