3-(5-PHENYL-1,3-OXAZOL-2-YL)PROPANOIC ACID

97%

  • Product Code: 120361
  CAS:    23485-68-9
Molecular Weight: 217.22 g./mol Molecular Formula: C₁₂H₁₁NO₃
EC Number: MDL Number: MFCD00713291
Melting Point: 149-153 °C Boiling Point:
Density: Storage Condition: room temperature
Product Description: 3-(5-Phenyl-1,3-oxazol-2-yl)propanoic acid is primarily utilized in the field of organic synthesis and medicinal chemistry. It serves as a key intermediate in the development of various pharmaceutical compounds. Its structure, featuring both an oxazole ring and a carboxylic acid group, makes it valuable for designing molecules with potential biological activity. This compound is often employed in the synthesis of anti-inflammatory and antimicrobial agents, where the oxazole moiety contributes to enhanced binding affinity and efficacy. Additionally, it is used in research to explore novel drug candidates targeting specific enzymes or receptors, particularly in the context of metabolic and inflammatory diseases. Its versatility in chemical reactions also makes it a useful building block in the creation of more complex organic molecules.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿3,366.00
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10.000 10-20 days ฿18,720.00
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3-(5-PHENYL-1,3-OXAZOL-2-YL)PROPANOIC ACID
3-(5-Phenyl-1,3-oxazol-2-yl)propanoic acid is primarily utilized in the field of organic synthesis and medicinal chemistry. It serves as a key intermediate in the development of various pharmaceutical compounds. Its structure, featuring both an oxazole ring and a carboxylic acid group, makes it valuable for designing molecules with potential biological activity. This compound is often employed in the synthesis of anti-inflammatory and antimicrobial agents, where the oxazole moiety contributes to enhanced binding affinity and efficacy. Additionally, it is used in research to explore novel drug candidates targeting specific enzymes or receptors, particularly in the context of metabolic and inflammatory diseases. Its versatility in chemical reactions also makes it a useful building block in the creation of more complex organic molecules.
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