848862-73-7

Basic information

• Product Name: 1-O-tert-butyldiphenylsilyl-5-O-benzyl-2,3-O-isopropylidene-4-keto-D-erythro-pentitol
• Synonyms: 1-O-tert-butyldiphenylsilyl-5-O-benzyl-2,3-O-isopropylidene-4-keto-D-erythro-pentitol
• CAS NO: 848862-73-7
• Molecular Weight: 518.725
• Mol File: 848862-73-7.mol

Chemical Properties

• CAS DataBase Reference: 1-O-tert-butyldiphenylsilyl-5-O-benzyl-2,3-O-isopropylidene-4-keto-D-erythro-pentitol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-O-tert-butyldiphenylsilyl-5-O-benzyl-2,3-O-isopropylidene-4-keto-D-erythro-pentitol(848862-73-7)
• EPA Substance Registry System: 1-O-tert-butyldiphenylsilyl-5-O-benzyl-2,3-O-isopropylidene-4-keto-D-erythro-pentitol(848862-73-7)

Safety Data

• Hazardous Substances Data: 848862-73-7(Hazardous Substances Data)

Upstream product

• 532-20-7 D-Ribose 
• 212003-35-5 allyl 5-O-benzyl-2,3-O-isopropylidene-β-D-ribofuranoside 
• 126862-99-5 (6-allyloxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methanol 
• 100-39-0 benzyl bromide 
• 198969-39-0 5-O-benzyl-2,3-O-isopropylidene-D-ribofuranose 
• 117248-94-9 5-O-benzyl-2,3-O-isopropylidene-D-ribitol 
• 117174-48-8 1-O-tert-butyldiphenylsilyl-5-O-benzyl-2,3-O-isopropylidene-D-ribitol 

Downstream Products

• 328396-52-7 (2S,3R)-5-benzyl-2,3-O-isopropylidene-4-C-methylene-2-C-vinyl-D-erythro-pentitol 
• 328396-53-8 (4R,5S)-(-)-3-[(benzyloxy)methyl]-4,5-O-isopropylidene-2-cyclopenten-1-ol 
• 117307-62-7 (3aR,6aR)-6-Benzyloxymethyl-2,2-dimethyl-4,6a-dihydro-3aH-cyclopenta[d][1,3]dioxol-4-one 
• 495397-67-6 (4R,5R)-5-(1-Benzyloxymethyl-vinyl)-2,2-dimethyl-[1,3]dioxolane-4-carbaldehyde 
• 130114-57-7 (2S,3R)-5-benzyl-2,3-O-isopropylidene-4-C-methylene-D-erytho-pentitol 
• 848862-75-9 1-O-tert-butyldiphenylsilyl-5-O-benzyl-2,3-O-isopropylidene-4-C-methylene-D-erythro-pentitol 

Relevant articles and documents

Synthetic studies toward the preparation of (4R,5R)-(-)-3-[(benzyloxy) methyl]-4,5-O-isopropylidene-cyclopenten-2-one: An important synthetic intermediate for carbanucleosides

The carbocyclic compound (4R,5R)-(-)-3-[(benzyloxy)methyl]-4,5-O- isopropylidene-2-cyclopentenone 1 is an important synthetic intermediate to access a variety of carbanucleosides. Herein, synthetic studies that lead to this valuable compound employing ine

Synthesis using ring closure metathesis and effect on nucleoside transport of a (N)-methanocarba S-(4-nitrobenzyl)thioinosine derivative

(Matrix presented) A new synthetic route to ring-constrained (N)-methanocarba nucleosides and nucleotides is presented. Ring closure of a diene intermediate usina Grubbs catalyst provides a new avenue for the preparation of the cyclopentenone derivative 6