127761-83-5

Basic information

• Product Name: 1,4-anhydro-5-O-(tert-butyldiphenylsilyl)-2-deoxy-D-erythro-pent-1-enitol
• Synonyms: 1,4-anhydro-5-O-(tert-butyldiphenylsilyl)-2-deoxy-D-erythro-pent-1-enitol
• CAS NO: 127761-83-5
• Molecular Weight: 354.521
• Mol File: 127761-83-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1,4-anhydro-5-O-(tert-butyldiphenylsilyl)-2-deoxy-D-erythro-pent-1-enitol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-anhydro-5-O-(tert-butyldiphenylsilyl)-2-deoxy-D-erythro-pent-1-enitol(127761-83-5)
• EPA Substance Registry System: 1,4-anhydro-5-O-(tert-butyldiphenylsilyl)-2-deoxy-D-erythro-pent-1-enitol(127761-83-5)

Safety Data

• Hazardous Substances Data: 127761-83-5(Hazardous Substances Data)

Upstream product

• 101527-40-6 5'-O-tert-butyldiphenylsilylthymidine 
• 50-89-5 thymidine 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 127791-68-8 1,4-anhydro-5-O-(tert-butyldiphenylsilyl)-2-deoxy-3-O-(trimethylsilyl)-D-erythro-pent-1-enitol 

Downstream Products

• 127761-87-9 (3R,4R)-3-(tert-Butyl-diphenyl-silanyloxymethyl)-2,6-dioxa-bicyclo[3.1.0]hexan-4-ol 
• 401813-15-8 (2S,3S)-2-(tert-butyldiphenylsilanyloxymethyl)tetrahydrofuran-3-ol 
• 263764-83-6 buergerinin G 
• 544687-62-9 (1S,5R)-1-(tosyloxymethyl)-7-methyl-2,6,8-trioxaspiro[4.5]decane 
• 544687-56-1 (2S)-2-(tert-butyldiphenylsilanyloxymethyl)-4,5-dihydro-2H-furan-3-one 
• 544687-57-2 (2S,3S)-2-(tert-butyldiphenylsilanyloxymethyl)-3-vinyltetrahydrofuran-3-ol 
• 544687-58-3 (2S,3R)-2-(tert-butyldiphenylsilanyloxymethyl)-3-(2'-hydroxyethyl)tetrahydrofuran-3-ol 
• 544687-59-4 (1S,5R)-1-(tert-butyldiphenylsilanyloxymethyl)-7-methyl-2,6,8-trioxaspiro[4.5]decane 
• 91547-59-0 (2R,3S)-2-(hydroxymethyl)tetrahydrofuran-3-ol 
• 95049-01-7 5-O-(4,4'-dimethoxytriphenylmethyl)-1,4-anhydro-2-deoxy-D-ribitol 

Relevant articles and documents

Synthesis of a New Furanoid Glycal Auxiliary

A route is investigated for the synthesis of 3-O-allyl-1,4-anhydro-5-O- tert-butyldiphenylsilyl-2-deoxy-D-erythro-pent-1-enitol. The highest overall yield was obtained when 5′-O-(tert-butyldiphenylsilyl)thymidine was converted to the corresponding furanoi

One-pot synthesis of β-N-glycosyl imidazole analogues via a palladium-catalysed decarboxylative allylation

A concise and highly efficient strategy for the synthesis of N-glycosyl imidazole analogues is reported. This reaction is based on a palladium catalysed decarboxylative allylation and three steps, namely, carbamation, decarboxylation and allylation are involved. All the substrates can afford the desired products with excellent yields and selectivities. the Partner Organisations 2014.