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

98%

Reagent Code: #202886
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CAS Number 1079-47-6

science Other reagents with same CAS 1079-47-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 302.06 g/mol
Formula C₉H₇IN₂O₂
badge Registry Numbers
MDL Number MFCD07371578
thermostat Physical Properties
Melting Point 264 °C
Boiling Point 421.4±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.948±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry, light-proof

description 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 Unit Price Quantity
inventory 1g
10-20 days ฿21,190.00
Methyl 5-iodo-1H-indazole-3-carboxylate
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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, enh

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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