2,3,5-Tri-O-benzyl-D-ribofuranose, 98%
2,3,5-Tri-O-benzyl-D-ribofuranose, 98%
2,3,5-Tri-O-benzyl-D-ribofuranose, 98%
Thermo Scientific Chemicals

2,3,5-Tri-O-benzyl-D-ribofuranose, 98%

CAS: 54623-25-5 | C26H28O5
Quantity:
1 g
5 g
Catalog number H33605.03
also known as H33605-03
Price (JPY)
-
Quantity:
1 g
Request bulk or custom format
Chemical Identifiers
CAS54623-25-5
SpecificationsSpecification SheetSpecification Sheet
FormPowder
Optical Rotation63.0 ± 4.0? (C=4 in DCM)
Appearance (Color)White
Assay (HPLC)≥97.5%
Melting Point (clear melt)48.0-55.0?C
It is used as pharmaceutical intermediate. Benzoylthiophenes are allosteric enhancers (AE) of agonist activity at the A1 adenosine receptor.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
It is used as pharmaceutical intermediate. Benzoylthiophenes are allosteric enhancers (AE) of agonist activity at the A1 adenosine receptor.

Solubility
Sparingly soluble in water.(0.26 g/L) (25°C),

Notes
Store in cool dry place. Ensure proper ventilation. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. C. Elisabet Tranberg.; Andrea Zickgraf.; Brian N. Giunta.; Henning Luetjens.; Heidi Figler.; Lauren J. Murphree.; Ruediger Falke.; Holger Fleischer.; Joel Linden.; Peter J. Scammells.; Ray. A. Olsson. 2-Amino-3-aroyl-4,5-alkylthiophenes:  Agonist Allosteric Enhancers at Human A1 Adenosine Receptors.J. Med. Chem. 2002, 45 (2),382-389 .
  2. Robert H. Dodd.; Catherine Ouannes.; Malka Robert-Gero.; Pierre Potier. Hybrid molecules: growth inhibition of Leishmania donovani promastigotes by thiosemicarbazones of 3-carboxy-.beta.-carbolines.J. Med. Chem. 1989, 32 (6),1272-1276 .