5-(Chloromethyl)-1H-indazole

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Reagent Code: #160755
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CAS Number 944904-22-7

science Other reagents with same CAS 944904-22-7

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Weight 166.61 g/mol
Formula C₈H₇ClN₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the preparation of pharmaceutical compounds. It plays a key role in the development of kinase inhibitors and other biologically active molecules due to its ability to form covalent bonds with target proteins. Commonly employed in medicinal chemistry for structure-activity relationship studies, particularly in cancer and inflammation research. Its reactive chloromethyl group allows for easy alkylation or conjugation with other functional groups, making it valuable in the design of drug candidates and biochemical probes.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿4,600.00
inventory 250mg
10-20 days ฿13,870.00
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5-(Chloromethyl)-1H-indazole
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Used primarily as an intermediate in organic synthesis, especially in the preparation of pharmaceutical compounds. It plays a key role in the development of kinase inhibitors and other biologically active molecules due to its ability to form covalent bonds with target proteins. Commonly employed in medicinal chemistry for structure-activity relationship studies, particularly in cancer and inflammation research. Its reactive chloromethyl group allows for easy alkylation or conjugation with other functiona

Used primarily as an intermediate in organic synthesis, especially in the preparation of pharmaceutical compounds. It plays a key role in the development of kinase inhibitors and other biologically active molecules due to its ability to form covalent bonds with target proteins. Commonly employed in medicinal chemistry for structure-activity relationship studies, particularly in cancer and inflammation research. Its reactive chloromethyl group allows for easy alkylation or conjugation with other functional groups, making it valuable in the design of drug candidates and biochemical probes.

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