3-Iodo-1,4,5,6-tetrahydrocyclopenta[c]pyrazole

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Reagent Code: #200451
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CAS Number 1426424-00-1

science Other reagents with same CAS 1426424-00-1

blur_circular Chemical Specifications

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Weight 234.04 g/mol
Formula C₆H₇IN₂
badge Registry Numbers
MDL Number MFCD26406995
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its iodine functionality allows for further functionalization via cross-coupling reactions such as Suzuki or Heck couplings, making it valuable in medicinal chemistry for building complex heterocyclic systems. It is also employed in the preparation of analogs for structure-activity relationship (SAR) studies due to its rigid, fused ring structure that can mimic peptide motifs or influence binding affinity in drug targets.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿730.00
inventory 250mg
10-20 days ฿1,026.00
inventory 1g
10-20 days ฿4,540.00
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3-Iodo-1,4,5,6-tetrahydrocyclopenta[c]pyrazole
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Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its iodine functionality allows for further functionalization via cross-coupling reactions such as Suzuki or Heck couplings, making it valuable in medicinal chemistry for building complex heterocyclic systems. It is also employed in the preparation of analogs for structure-activity relationship (SAR) studies due to its rigid, fuse

Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its iodine functionality allows for further functionalization via cross-coupling reactions such as Suzuki or Heck couplings, making it valuable in medicinal chemistry for building complex heterocyclic systems. It is also employed in the preparation of analogs for structure-activity relationship (SAR) studies due to its rigid, fused ring structure that can mimic peptide motifs or influence binding affinity in drug targets.

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