(2R,3R,4R,5R)-5-(4-Benzamido-2-oxopyrimidin-1(2H)-yl)-2-((benzoyloxy)methyl)-4-fluoro-4-methyltetrahydrofuran-3-yl benzoate

98%

  • Product Code: 73939
  CAS:    817204-32-3
Molecular Weight: 571.55 g./mol Molecular Formula: C₃₁H₂₆FN₃O₇
EC Number: MDL Number: MFCD23106344
Melting Point: Boiling Point:
Density: Storage Condition: -20°C, dry sealed
Product Description: This compound is primarily utilized in the field of medicinal chemistry and drug development, particularly in the synthesis of nucleoside analogs. These analogs are critical in the creation of antiviral and anticancer agents, as they can interfere with the replication of viral DNA or RNA, or inhibit the growth of cancer cells. The presence of the benzamido and benzoyl groups in its structure enhances its stability and bioavailability, making it a valuable intermediate in the production of therapeutic drugs. Additionally, its fluorinated tetrahydrofuran moiety contributes to its potential use in targeted therapies, where fluorine atoms are often incorporated to improve binding affinity and metabolic stability. Researchers also explore its application in the development of prodrugs, which are designed to release active pharmaceutical ingredients in a controlled manner within the body.
Product Specification:
Test Specification
APPEARANCE White to off-white Solid
PURITY 97.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days $23.10
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-
5.000 10-20 days $64.29
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10.000 10-20 days $114.52
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-
25.000 10-20 days $282.27
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(2R,3R,4R,5R)-5-(4-Benzamido-2-oxopyrimidin-1(2H)-yl)-2-((benzoyloxy)methyl)-4-fluoro-4-methyltetrahydrofuran-3-yl benzoate
This compound is primarily utilized in the field of medicinal chemistry and drug development, particularly in the synthesis of nucleoside analogs. These analogs are critical in the creation of antiviral and anticancer agents, as they can interfere with the replication of viral DNA or RNA, or inhibit the growth of cancer cells. The presence of the benzamido and benzoyl groups in its structure enhances its stability and bioavailability, making it a valuable intermediate in the production of therapeutic drugs. Additionally, its fluorinated tetrahydrofuran moiety contributes to its potential use in targeted therapies, where fluorine atoms are often incorporated to improve binding affinity and metabolic stability. Researchers also explore its application in the development of prodrugs, which are designed to release active pharmaceutical ingredients in a controlled manner within the body.
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