Product Description
Chemical Name: (2R)-N-Benzoyl-2-deoxy-2-fluoro-2-methylcytidine3,5-dibenzoate
Synonyms : (2R)-N-Benzoyl-2-deoxy-2-fluoro-2-Methylcytidine3,5-dibenzoate |
Cytidine,N-benzoyl-2-deoxy-2-fluoro-2-methyl-, 3,5-dibenzoate,(2R)-
|
Cytidine, N-benzoyl-2-deoxy-2-fluoro-2-methyl-,3,5-dibenzoate, (2R)- |
(2R)-N-benzoyl-2-deoxy-2-fluoro-2-methyl-3,5-dibenzoateCytidine |
[(2R,3R,4R,5R)-5-(4-benzamido-2-oxopyrimidin-1-yl)-3-benzoyloxy-4-fluoro-4-methyloxolan-2-yl]methylbenzoate |
Cytidine,N-benzoyl-2-deoxy-2-fluoro-2-methyl-,3,5-dibenzoate,(2R)-
CAS No : 817204-32-3
Purity : 97%
Molecular Formula :C31H26FN3O7
Molecular Weight: 571.6
Appearance: SolidVersatile Research ApplicationThis compound is utilized predominantly as a synthetic intermediate in the design and synthesis of advanced nucleoside analogues. Its modified structure, featuring both fluorine and methyl groups, enhances its utility in pharmaceutical R&D and antiviral investigations. Researchers benefit from its high purity and stability, ensuring reliable results in complex organic syntheses.
Proper Storage and HandlingTo ensure optimal stability and prevent degradation, store the product in a tightly sealed container within a desiccated environment at 28C, away from light and moisture. Amber vials protect the material from photodegradation, supporting a shelf life of up to two years. Always handle in a controlled laboratory setting, using appropriate personal protective equipment.
FAQs of (2R)-N-Benzoyl-2-deoxy-2-fluoro-2-methylcytidine 3,5-dibenzoate:
Q: How should (2R)-N-Benzoyl-2-deoxy-2-fluoro-2-methylcytidine 3,5-dibenzoate be stored for maximum stability?
A: Store this compound in a tightly sealed, desiccated container at 2-8C, protected from light and moisture, to ensure stability and maintain its 98% purity. The use of amber glass vials is recommended.
Q: What is the main application of this nucleoside derivative in research?
A: It is primarily used as a synthetic intermediate in laboratory research, particularly for the synthesis of nucleoside analogues and as a precursor in pharmaceutical R&D and antiviral drug development.
Q: When is it recommended to use this compound during pharmaceutical synthesis?
A: It should be employed at intermediate stages of nucleoside analogue synthesis, offering enhanced efficacy due to its modified base structure. This makes it valuable in pharmaceutical and antiviral research pipelines.
Q: Where can I obtain (2R)-N-Benzoyl-2-deoxy-2-fluoro-2-methylcytidine 3,5-dibenzoate?
A: You can source this compound from reputable chemical suppliers or traders specializing in research-grade materials, especially those operating from India or providing global shipping.
Q: What is the process for using this compound in the laboratory?
A: Dissolve the compound in DMSO for optimal solubility, or in methanol/ethanol to a lesser extent. Ensure all work is conducted in a laboratory environment, complying with safety protocols for handling chemical intermediates.
Q: What benefits does this compound offer over standard nucleosides?
A: Its fluorine and methyl modifications confer greater stability, enhanced biochemical activity, and greater suitability for pharmaceutical R&D, particularly in the exploration of antiviral therapies.