Methyl 5-iodo-1H-indazole-3-carboxylate

98%

  • Product Code: 202886
  CAS:    1079-47-6
Molecular Weight: 302.06 g./mol Molecular Formula: C₉H₇IN₂O₂
EC Number: MDL Number: MFCD07371578
Melting Point: 264 °C Boiling Point: 421.4±25.0 °C(Predicted)
Density: 1.948±0.06 g/cm3(Predicted) Storage Condition: 2-8°C, sealed, dry, light-proof
Product Description: Used primarily as a key intermediate in the synthesis of bioactive compounds, particularly in pharmaceutical research. It serves as a building block for developing kinase inhibitors and other medicinal agents targeting cancer and inflammatory diseases. The presence of the iodine atom allows for further functionalization via cross-coupling reactions, such as Suzuki or Heck reactions, enabling rapid diversification in drug discovery programs. Its indazole core is valued for mimicking purine structures, enhancing binding affinity to enzyme active sites. Commonly employed in the development of selective inhibitors for proteins like B-Raf, JAK, or CDK, it supports the creation of potential therapeutics in oncology and autoimmune disorders. Also utilized in radiolabeling studies and probe development for biochemical assays due to the iodine moiety.
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Size Availability Price Quantity
1g 10-20 days ฿21,190.00
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Methyl 5-iodo-1H-indazole-3-carboxylate
Used primarily as a key intermediate in the synthesis of bioactive compounds, particularly in pharmaceutical research. It serves as a building block for developing kinase inhibitors and other medicinal agents targeting cancer and inflammatory diseases. The presence of the iodine atom allows for further functionalization via cross-coupling reactions, such as Suzuki or Heck reactions, enabling rapid diversification in drug discovery programs. Its indazole core is valued for mimicking purine structures, enhancing binding affinity to enzyme active sites. Commonly employed in the development of selective inhibitors for proteins like B-Raf, JAK, or CDK, it supports the creation of potential therapeutics in oncology and autoimmune disorders. Also utilized in radiolabeling studies and probe development for biochemical assays due to the iodine moiety.
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