The chemical substance known as "(3S,4S,5R)-5-(benzoyloxymethyl)-4-fluorotetrahydrofuran-2,3-diyl diacetate," with the CAS number 159099-24-8, is a complex organic compound characterized by its tetrahydrofuran ring structure, which is a five-membered cyclic ether. This compound features multiple functional groups, including a fluorine atom, acetyl groups, and a benzoyloxymethyl moiety, contributing to its reactivity and potential applications in organic synthesis. The stereochemistry indicated by the (3S,4S,5R) configuration suggests specific spatial arrangements of atoms, which can influence the compound's biological activity and interactions. The presence of the fluorine atom may enhance lipophilicity and metabolic stability, while the benzoyloxymethyl group can provide sites for further chemical modifications. Overall, this compound's unique structural features make it of interest in medicinal chemistry and drug development, particularly in the design of novel therapeutic agents. Its properties, such as solubility, stability, and reactivity, would be influenced by the specific arrangement of its functional groups and stereochemistry.

(3S,4S,5R)-5-(benzoyloxymethyl)-4-fluorotetrahydrofuran-2,3-diyl diacetate

159099-24-8: The chemical substance known as "(3S,4S,5R)-5-(benzoyloxymethyl)-4-fluorotetrahydrofuran-2,3-diyl diacetate," with the CAS number 159099-24-8, is a complex organic compound characterized by its tetrahydrofuran ring structure, which is a five-membered cyclic ether. This compound features multiple functional groups, including a fluorine atom, acetyl groups, and a benzoyloxymethyl moiety, contributing to its reactivity and potential applications in organic synthesis. The stereochemistry indicated by the (3S,4S,5R) configuration suggests specific spatial arrangements of atoms, which can influence the compound's biological activity and interactions. The presence of the fluorine atom may enhance lipophilicity and metabolic stability, while the benzoyloxymethyl group can provide sites for further chemical modifications. Overall, this compound's unique structural features make it of interest in medicinal chemistry and drug development, particularly in the design of novel therapeutic agents. Its properties, such as solubility, stability, and reactivity, would be influenced by the specific arrangement of its functional groups and stereochemistry.

<p>1,2-Di-O-acetyl-5-O-benzoyl-3-deoxy-3-fluoro-D-xylofuranose is a Carbohydrate Derivative.</p>

1,2-Di-O-acetyl-5-O-benzoyl-3-deoxy-3-fluoro-D-xylofuranose

<p>1,2-Di-O-acetyl-5-O-benzoyl-3-deoxy-3-fluoro-D-ribofuranose is a methylated saccharide. It has been modified with a click modification and has been synthesized using glycosylation and Oligosaccharides. This product can be used for custom synthesis and is available in high purity and with a CAS No. 159099-24-8. The molecular weight of this compound is 386.14 g/mol.</p>

CAS 159099-24-8

(3S,4S,5R)-5-(benzoyloxymethyl)-4-fluorotetrahydrofuran-2,3-diyl diacetate

1,2-Di-O-acetyl-5-O-benzoyl-3-deoxy-3-fluoro-D-xylofuranose

Ref: TM-TNU0899

1,2-Di-O-acetyl-5-O-benzoyl-3-deoxy-3-fluoro-D-ribofuranose

Ref: 3D-FD144993