187879-14-7

Basic information

• Product Name: 1,5-Anhydro-2-deoxy-4,6-O-[(R)-(4-methoxyphenyl)methylene]-3-O-[tris(1-methylethyl)silyl]-D-arabino-hex-1-enitol
• Synonyms: 1,5-Anhydro-2-deoxy-4,6-O-[(R)-(4-methoxyphenyl)methylene]-3-O-[tris(1-methylethyl)silyl]-D-arabino-hex-1-enitol
• CAS NO: 187879-14-7
• Molecular Weight: 420.621
• Mol File: 187879-14-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1,5-Anhydro-2-deoxy-4,6-O-[(R)-(4-methoxyphenyl)methylene]-3-O-[tris(1-methylethyl)silyl]-D-arabino-hex-1-enitol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,5-Anhydro-2-deoxy-4,6-O-[(R)-(4-methoxyphenyl)methylene]-3-O-[tris(1-methylethyl)silyl]-D-arabino-hex-1-enitol(187879-14-7)
• EPA Substance Registry System: 1,5-Anhydro-2-deoxy-4,6-O-[(R)-(4-methoxyphenyl)methylene]-3-O-[tris(1-methylethyl)silyl]-D-arabino-hex-1-enitol(187879-14-7)

Safety Data

• Hazardous Substances Data: 187879-14-7(Hazardous Substances Data)

Upstream product

• 13265-84-4 D-glucal 
• 13154-24-0 triisopropylsilyl chloride 
• 187880-20-2 2,6-anhydro-5-deoxy-1,3-O-(4-methoxybenzylidene)-D-arabino-hex-5-enitol 
• 2186-92-7 p-Anisaldehyde dimethyl acetal 

Downstream Products

• 199116-19-3 C₈₀H₁₀₂O₁₅Si₂ 
• 196704-96-8 4-O-p-methoxybenzyl-D-glucal 
• 199116-18-2 4-O-(4-methoxybenzyl)-3-O-(triisopropyl)silyl-D-glucal 
• 629652-50-2 (2R,3R,4S,4aR,7R,8R,9aR)-3,4-Bis-benzyloxy-2-benzyloxymethyl-8-(4-methoxy-benzyloxy)-7-(4-methoxy-benzyloxymethyl)-2,3,4a,7,8,9a-hexahydro-4H-1,6,9-trioxa-10-thia-anthracen-5-one 
• 629652-43-3 4,6-di-O-(4-methoxybenzyl)-2-deoxy-3-O-(triisopropyl)silyl-α,β-D-glucopyranose 
• 629652-41-1 4,6-di-O-(4-methoxybenzyl)-3-O-(triisopropyl)silyl-D-(-)-glucal 
• 629652-49-9 2-deoxy-1,3-dioxo-4,6-di-O-(4-methoxybenzyl)-D-(+)-glucopyranose 
• 629652-48-8 2-deoxy-4,6-di-O-(4-methoxybenzyl)-D-gluco-γ-lactone 
• 629652-46-6 4,6-di-O-(4-methoxybenzyl)-2-deoxy-α,β-D-glucopyranose 

Relevant articles and documents

Totally Stereoselective Synthesis of 1,3-Disaccharides through Diels-Alder Reactions

A nonclassical, totally stereoselective synthesis of orthogonally protected 1,3-disaccharides is reported. Enantiomerically pure β-keto-δ-lactones, efficiently obtained from glucal and galactal, are transformed into electron-poor heterodienes and chemo-,