Methyl 5-chloro-3-iodo-1H-indazole-6-carboxylate

≥95%

Reagent Code: #208667
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CAS Number 1227270-79-2

science Other reagents with same CAS 1227270-79-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 336.51 g/mol
Formula C₉H₆ClIN₂O₂
badge Registry Numbers
MDL Number MFCD16875822
thermostat Physical Properties
Boiling Point 451.4±40.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used in pharmaceutical research as an intermediate in the synthesis of biologically active compounds, particularly in the development of kinase inhibitors and anticancer agents. Its structure supports derivatization for structure-activity relationship (SAR) studies, making it valuable in drug discovery programs targeting oncology and inflammatory diseases. The presence of halogen atoms allows for cross-coupling reactions, enabling the introduction of various functional groups to optimize potency and selectivity.

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inventory 1g
10-20 days ฿20,660.00

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Methyl 5-chloro-3-iodo-1H-indazole-6-carboxylate
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Used in pharmaceutical research as an intermediate in the synthesis of biologically active compounds, particularly in the development of kinase inhibitors and anticancer agents. Its structure supports derivatization for structure-activity relationship (SAR) studies, making it valuable in drug discovery programs targeting oncology and inflammatory diseases. The presence of halogen atoms allows for cross-coupling reactions, enabling the introduction of various functional groups to optimize potency and selecti
Used in pharmaceutical research as an intermediate in the synthesis of biologically active compounds, particularly in the development of kinase inhibitors and anticancer agents. Its structure supports derivatization for structure-activity relationship (SAR) studies, making it valuable in drug discovery programs targeting oncology and inflammatory diseases. The presence of halogen atoms allows for cross-coupling reactions, enabling the introduction of various functional groups to optimize potency and selectivity.
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