808761-99-1

Basic information

• Product Name: phenyl 4,6-O-p-methoxybenzylidene-1-thio-α-D-mannopyranoside
• Synonyms: phenyl 4,6-O-p-methoxybenzylidene-1-thio-α-D-mannopyranoside
• CAS NO: 808761-99-1
• Molecular Weight: 390.457
• Mol File: 808761-99-1.mol

Chemical Properties

• CAS DataBase Reference: phenyl 4,6-O-p-methoxybenzylidene-1-thio-α-D-mannopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: phenyl 4,6-O-p-methoxybenzylidene-1-thio-α-D-mannopyranoside(808761-99-1)
• EPA Substance Registry System: phenyl 4,6-O-p-methoxybenzylidene-1-thio-α-D-mannopyranoside(808761-99-1)

Safety Data

• Hazardous Substances Data: 808761-99-1(Hazardous Substances Data)

Upstream product

• 2186-92-7 p-Anisaldehyde dimethyl acetal 
• 2936-70-1 (2R,3S,4S,5S,6R)-2-Hydroxymethyl-6-phenylsulfanyl-tetrahydro-pyran-3,4,5-triol 

Downstream Products

• 902751-14-8 phenyl 3-O-allyl-2-O-benzyl-4,6-O-(p-methoxybenzylidene)-α-D-thiomannopyranoside 
• 902751-23-9 phenyl 2-O-benzyl-4,6-O-(p-methoxybenzylidene)-3-O-(2-naphthalenylmethyl)-α-D-thiomannopyranoside 
• 1008750-57-9 phenyl 3-O-p-methoxybenzyl-4,6-O-p-methoxybenzylidene-1-thio-α-D-mannopyranoside 
• 808762-01-8 phenyl 2,3-di-O-benzyl-4,6-O-p-methoxybenzylidene-1-thio-α-D-mannopyranoside 

Relevant articles and documents

Thieme chemistry journal awardees - where are they now? synthesis of the marine glycolipid dioctadecanoyl discoside

The first synthesis of the inositol-containing marine glycolipid dioctadecanoyl discoside is reported. The key glycosylation reaction proceeds with β-selectivity at reduced temperature. The separable anomers could be readily progressed to afford discoside

Direct chemical synthesis of the β-mannans: Linear and block syntheses of the alternating β-(1→3)-β-(1→4)-mannan common to Rhodotorula glutinis, Rhodotorula mucilaginosa, and Leptospira biflexa

Two stereocontrolled syntheses of a methyl glycoside of an alternating β-(1→4)-β-(1→3)-mannohexaose, representative of the mannan from Rhodotorula glutinis, Rhodotorula mucilaginosa, and Leptospira biflexa, are described. Both syntheses employ a combinati