2-(2-(5-Methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl)acetamido)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxamide

98%

  • Product Code: 41310
  CAS:    489408-02-8
Molecular Weight: 386.3900 g./mol Molecular Formula: C₁₆H₁₇F₃N₄O₂S
EC Number: MDL Number: MFCD02053612
Melting Point: Boiling Point:
Density: Storage Condition: room temperature
Product Description: This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. It is often employed in the development of pharmaceutical agents targeting specific enzyme pathways, particularly those involved in inflammatory and metabolic disorders. Its structural features, including the pyrazole and tetrahydrobenzo[b]thiophene moieties, make it a valuable scaffold for designing inhibitors or modulators of protein interactions. Researchers also explore its potential in creating novel therapeutics for conditions such as cancer, autoimmune diseases, and neurological disorders due to its ability to interact with diverse biological targets. Additionally, its trifluoromethyl group enhances its metabolic stability and binding affinity, making it a promising candidate for drug discovery programs.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿468.00
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2-(2-(5-Methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl)acetamido)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxamide
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. It is often employed in the development of pharmaceutical agents targeting specific enzyme pathways, particularly those involved in inflammatory and metabolic disorders. Its structural features, including the pyrazole and tetrahydrobenzo[b]thiophene moieties, make it a valuable scaffold for designing inhibitors or modulators of protein interactions. Researchers also explore its potential in creating novel therapeutics for conditions such as cancer, autoimmune diseases, and neurological disorders due to its ability to interact with diverse biological targets. Additionally, its trifluoromethyl group enhances its metabolic stability and binding affinity, making it a promising candidate for drug discovery programs.
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