3-(5-Methyl-1,3,4-thiadiazol-2-yl)propanoic acid

95%

  • Product Code: 86731
  CAS:    205383-48-8
Molecular Weight: 172.20 g./mol Molecular Formula: C₆H₈N₂O₂S
EC Number: MDL Number: MFCD21880503
Melting Point: Boiling Point: 381.3±25.0 °C(Predicted)
Density: 1.371±0.06 g/cm3(Predicted) Storage Condition: room temperature
Product Description: 3-(5-Methyl-1,3,4-thiadiazol-2-yl)propanoic acid finds its application primarily in the field of medicinal chemistry and pharmaceutical research. It is often utilized as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting enzyme inhibition or receptor modulation. The thiadiazole ring in its structure is known to impart significant pharmacological properties, making it valuable in the development of potential drugs for treating diseases such as cancer, bacterial infections, and inflammatory conditions. Additionally, its carboxylic acid group allows for further functionalization, enabling the creation of derivatives with enhanced therapeutic efficacy. Researchers also explore its use in designing novel agrochemicals, leveraging its structural features to develop compounds with herbicidal or pesticidal activity.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿16,740.00
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0.250 10-20 days ฿31,500.00
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3-(5-Methyl-1,3,4-thiadiazol-2-yl)propanoic acid
3-(5-Methyl-1,3,4-thiadiazol-2-yl)propanoic acid finds its application primarily in the field of medicinal chemistry and pharmaceutical research. It is often utilized as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting enzyme inhibition or receptor modulation. The thiadiazole ring in its structure is known to impart significant pharmacological properties, making it valuable in the development of potential drugs for treating diseases such as cancer, bacterial infections, and inflammatory conditions. Additionally, its carboxylic acid group allows for further functionalization, enabling the creation of derivatives with enhanced therapeutic efficacy. Researchers also explore its use in designing novel agrochemicals, leveraging its structural features to develop compounds with herbicidal or pesticidal activity.
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