6-Bromo-3-cyclopropyl-1H-indazole

95%

  • Product Code: 87660
  CAS:    1311197-90-6
Molecular Weight: 237.1 g./mol Molecular Formula: C₁₀H₉BrN₂
EC Number: MDL Number: MFCD19237233
Melting Point: Boiling Point: 394.2±22.0 °C at 760 mmHg
Density: Storage Condition: 2-8°C, sealed, dry
Product Description: 6-Bromo-3-cyclopropyl-1H-indazole is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active compounds. Its structure, featuring both a bromo substituent and a cyclopropyl group, makes it a versatile building block for the development of potential drug candidates. Researchers often employ it in the design and synthesis of small molecules that target specific enzymes or receptors, particularly in the areas of oncology and inflammation. Additionally, its indazole core is valuable in creating compounds with potential therapeutic applications, such as kinase inhibitors, which are crucial in treating cancers and other diseases. The compound’s unique structure also allows for further functionalization, enabling the exploration of diverse chemical spaces in drug discovery projects.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days ฿7,020.00
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1.000 10-20 days ฿14,040.00
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6-Bromo-3-cyclopropyl-1H-indazole
6-Bromo-3-cyclopropyl-1H-indazole is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active compounds. Its structure, featuring both a bromo substituent and a cyclopropyl group, makes it a versatile building block for the development of potential drug candidates. Researchers often employ it in the design and synthesis of small molecules that target specific enzymes or receptors, particularly in the areas of oncology and inflammation. Additionally, its indazole core is valuable in creating compounds with potential therapeutic applications, such as kinase inhibitors, which are crucial in treating cancers and other diseases. The compound’s unique structure also allows for further functionalization, enabling the exploration of diverse chemical spaces in drug discovery projects.
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