6974-32-9 | 1-O-Acetyl-2,3,5-tri-o-benzoyl-beta-D-ribofuranose

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$8.00	$5.00
10g	98%	in stock	$9.00	$6.00
25g	98%	in stock	$15.00	$10.00
100g	98%	in stock	$40.00	$28.00

Description

• Catalog Number: AC89676
• Chemical Name: 1-O-Acetyl-2,3,5-tri-o-benzoyl-beta-D-ribofuranose
• CAS Number: 6974-32-9
• Molecular Formula: C28H24O9
• Molecular Weight: 504.4848
• MDL Number: MFCD00005357
• SMILES: CC(=O)O[C@@H]1O[C@@H]([C@H]([C@H]1OC(=O)c1ccccc1)OC(=O)c1ccccc1)COC(=O)c1ccccc1

Computed Properties

• Complexity: 794
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 4
• Heavy Atom Count: 37
• Hydrogen Bond Acceptor Count: 9
• Rotatable Bond Count: 12
• XLogP3: 5.6

Literature

• Studies on the glycosylation of pyrrolo[2,3-d] pyrimidines with 1-O-acetyl-2,3,5-tri-O-benzoyl-beta-D-ribofuranose: the formation of regioisomers during toyocamycin and 7-deazainosine syntheses.

  Nucleosides, nucleotides & nucleic acids 20090501

• 7-deazainosine derivatives: synthesis and characterization of 7- and 7,8-substituted pyrrolo [2,3-d]pyrimidine ribonucleosides.

  Nucleosides, nucleotides & nucleic acids 20080501

• Regioselective glycosylation of 7-azapteridines and conversion of the 7-azapteridine nucleosides into 6-azapurine nucleosides.

  Nucleic acids symposium series (2004) 20080101

• Pyrazolo[3,4-d]pyrimidine ribonucleosides related to 2-aminoadenosine and isoguanosine: synthesis, deamination and tautomerism.

  Organic & biomolecular chemistry 20070921

• Synthesis of 2'-O-beta-d-Ribofuranosylnucleosides.

  Current protocols in nucleic acid chemistry 20070101

• 1,N6-Etheno-7-deaza-2,8-diazaadenosine: syntheses, properties and conversion to 7-deaza-2,8-diazaadenosine.

  Organic & biomolecular chemistry 20050507

• Synthesis of some novel N-ribosyl-1,2,4-triazin-6(1H)-/ones or thiones as potential antibacterial and antifungal chemotherapeutics.

  Nucleosides, nucleotides & nucleic acids 20050101

• Natural phosphate doped with KI in HMDS: a mild and efficient reagent for alkylation and glycosylation of nucleobases.

  Nucleosides, nucleotides & nucleic acids 20050101

• Synthesis of unnatural sugar nucleotides and their evaluation as donor substrates in glycosyltransferase-catalyzed reactions.

  Carbohydrate research 20041115

• Nucleosides. LXV. Synthesis of new pteridine-N8-nucleosides.

  Nucleosides, nucleotides & nucleic acids 20040101

• Synthesis and antiviral evaluation of isatin ribonucleosides.

  Nucleosides, nucleotides & nucleic acids 20020101