CAS 171866-30-1

1,3,5-TRI-O-BENZOYL-ALPHA-L-RIBOFURANOSE

Description:

1,3,5-Tri-O-benzoyl-alpha-L-ribofuranose is a chemical compound that belongs to the class of ribofuranosides, which are derivatives of ribose sugar. This compound features three benzoyl groups attached to the hydroxyl positions of the ribofuranose, enhancing its lipophilicity and stability compared to unmodified ribose. The presence of these benzoyl groups can influence its solubility and reactivity, making it useful in various organic synthesis applications, particularly in the field of carbohydrate chemistry. The alpha configuration indicates the orientation of the hydroxyl group at the anomeric carbon, which is significant for its biological activity and interactions. This compound is often utilized as an intermediate in the synthesis of nucleosides and other biologically relevant molecules. Its CAS number, 171866-30-1, uniquely identifies it in chemical databases, facilitating research and development in medicinal chemistry and related fields. Overall, 1,3,5-tri-O-benzoyl-alpha-L-ribofuranose is a valuable compound in synthetic organic chemistry, particularly for those studying carbohydrate derivatives.

Formula: C₂₆H₂₂O₈

Synonyms:

• 1,3,5-TRI-O-BENZOYL-ALPHA-L-RIBOFURANOSE
• 1,3,5-Tri-O-benzoyl-α-L-ribofuranose
• 1,3,5-Tri-O-benzoyl-a-L-ribofuranose
• alpha-L-Ribofuranose 1,3,5-tribenzoate
• α-L-Ribofuranose, 1,3,5-tribenzoate
• 1,3,5-TRI-O-BENZOYL-Α-L-RIBOFURANOSE

1,3,5-Tri-O-benzoyl-α-L-ribofuranose

CAS: 171866-30-1

Formula: C₂₆H₂₂O₈

Purity: 96%

Color and Shape: Solid

Molecular weight: 462.4481

Ref: IN-DA00ANQ2

1,3,5-Tri-O-benzoyl-a-L-ribofuranose

CAS: 171866-30-1

1,3,5-Tri-O-benzoyl-a-L-ribofuranose is a synthetic sugar with a complex carbohydrate structure. It is synthesized by the sequential addition of benzoyl groups to the alditol acetal of ribose. The molecular weight of this compound is 598.6 g/mol and its CAS number is 171866-30-1. 1,3,5-Tri-O-benzoyl-a-L-ribofuranose has been shown to be an excellent substrate for glycosylation and methylation reactions due to the presence of three reactive hydroxyl groups that can react with nucleophiles such as amines or thiols. Methylation reactions are typically carried out in the presence of sodium methoxide in methanol at room temperature for several hours. Glycosylation reactions require the use of activated glycosyl donors such as UDP glucose, UDP galactose

Formula: C₂₆H₂₂O₈

Purity: Min. 97 Area-%

Color and Shape: Powder

Molecular weight: 462.45 g/mol

Ref: 3D-MT44537