16205-59-7

Basic information

• Product Name: 2,3,5-tri-O-benzoyl-1-bromo-α-D-erythro-pentofuranose
• Synonyms: 2,3,5-tri-O-benzoyl-1-bromo-α-D-erythro-pentofuranose
• CAS NO: 16205-59-7
• Molecular Weight: 525.353
• Mol File: 16205-59-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2,3,5-tri-O-benzoyl-1-bromo-α-D-erythro-pentofuranose(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,5-tri-O-benzoyl-1-bromo-α-D-erythro-pentofuranose(16205-59-7)
• EPA Substance Registry System: 2,3,5-tri-O-benzoyl-1-bromo-α-D-erythro-pentofuranose(16205-59-7)

Safety Data

• Hazardous Substances Data: 16205-59-7(Hazardous Substances Data)

Upstream product

• 115459-50-2 2,3,5-Tri-O-benzoyl-D-ribofuranose 
• 6974-32-9 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose 

Downstream Products

• 457067-55-9 phenyl 2,3,5-tri-O-benzoyl-1-thio-β-D-ribofuranoside 
• 1748-04-5 tribenzoyl uridine 
• 88999-59-1 (3aR,5R,5aS,8aS,8bR)-5-((((2S,3R,4R,5R)-3,4-Bis(benzyloxy)-5-((benzyloxy)methyl)tetrahydrofuran-2-yl)oxy)methyl)-2,2,7,7-tetramethyltetrahydro-5H-bis([1,3]dioxolo)[4,5-b:4',5'-d]pyran 
• 140186-55-6 1,2:5,6-di-O-isopropylidene-3-O-(2,3,5-tri-O-benzyl-α-D-ribofuranosyl)-α-D-glucofuranoside 
• 140186-66-9 methyl (2,3,5-tri-O-benzyl-α-D-ribofuranosyl)-(1→5)-2,3-O-isopropylidene-β-D-ribofuranoside 
• 96689-78-0 2-pyridyl 2,3,5-tri-O-benzyl-1-thio-β-D-ribofuranoside 
• 35867-79-9 4-amino-8-(2,3,5-tri-O-benzoyl-β-D-erythro-pentofuranosyl)-7(8H)-pteridone 
• 79378-82-8 4-amino-2-phenyl-8-(2,3,5-tri-O-benzoyl-β-D-erythro-pentofuranosyl)-7(8H)-pteridone 
• 79378-84-0 4-amino-2,6-diphenyl-8-(2,3,5-tri-O-benzoyl-β-D-erythro-pentofuranosyl)-7(8H)-pteridone 
• 73978-57-1 7-Hydroxy-6-phenyl-1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)lumazin 
• 73990-92-8 7-Hydroxy-1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)lumazin 
• 73978-61-7 7-Hydroxy-1,3-bis(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)lumazin 
• 140186-54-5 C₃₁H₂₅NO₇S 
• 113575-02-3 1,2--α-D-ribofuranose 

Relevant articles and documents

COMPOUNDS AND METHODS USED IN ASSESSING MONO-PARP ACTIVITY

Mutant mono ADP-ribose-polymerases (mono-PARP) proteins and small molecule compound substrates specific for the mutant mono-PARP proteins as well as methods of using these compositions to identify protein targets of the mono-PARPs and to screen for antagonists of the mono-PARPs are described.

Appel-reagent-mediated transformation of glycosyl hemiacetal derivatives into thioglycosides and glycosyl thiols

A series of glycosyl hemiacetal derivatives have been transformed into thioglycosides and glycosyl thiols in a one-pot two-step reaction sequence mediated by Appel reagent (carbon tetrabromide and triphenylphosphine). 1,2-trans-Thioglycosides and β-glycosyl thiol derivatives were stereoselectively formed by the reaction of the in situ generated glycosyl bromides with thiols and sodium carbonotrithioate. The reaction conditions are reasonably simple and yields were very good.