4-Chloro-1H-indazol-6-amine

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Reagent Code: #160715
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CAS Number 221681-84-1

science Other reagents with same CAS 221681-84-1

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scatter_plot Molecular Information
Weight 167.6 g/mol
Formula C₇H₆ClN₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form stable heterocyclic structures that interact with biological targets. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) targeting inflammatory diseases and neurological disorders. Its amine and chloro functional groups allow for easy modification, enabling the creation of diverse compound libraries for drug discovery. Also utilized in agrochemical research for designing bioactive molecules with pesticidal or herbicidal activity.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,680.00

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4-Chloro-1H-indazol-6-amine
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form stable heterocyclic structures that interact with biological targets. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) targeting inflammatory diseases and neurological disorders. Its amine and chloro functional groups allow for easy modification, en

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form stable heterocyclic structures that interact with biological targets. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) targeting inflammatory diseases and neurological disorders. Its amine and chloro functional groups allow for easy modification, enabling the creation of diverse compound libraries for drug discovery. Also utilized in agrochemical research for designing bioactive molecules with pesticidal or herbicidal activity.

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