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Intermediates 6-bromo-3-iodo-1H-indazole for critical molecular building block
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Intermediates 6-bromo-3-iodo-1H-indazole for critical molecular building block

CAS:885521-88-0 

Product purity:98% Appearance: Yellowish brown solid

6-Bromo-3-iodo-1H-indazole | A Versatile Molecular Building Block

6-Bromo-3-iodo-1H-indazole is a high-purity, bifunctionalized indazole derivative designed for advanced pharmaceutical research and drug discovery. This compound serves as an exceptional molecular building block, featuring both bromo and iodo substituents at the 6 and 3 positions of the indazole core. These halogen atoms offer distinct and complementary reactivity profiles, enabling sequential cross-coupling reactions, such as Suzuki-Miyaura and Sonogashira couplings.

This versatility allows for systematic and diverse structural elaboration, making it an invaluable scaffold for constructing targeted compound libraries. It is particularly useful in medicinal chemistry for developing kinase inhibitors and other small molecule therapeutics. Our product guarantees superior quality, batch-to-batch consistency, and is supported by comprehensive analytical data (HPLC, NMR, MS).

    Product Detailed Information: 6-Bromo-3-iodo-1H-indazole

    CAS Number: 885521-88-0 

    Molecular Formula: C₇H₄BrIN₂

    Molecular Weight: 322.93 g/mol

    Introduction:

    6-Bromo-3-iodo-1H-indazole is a premium, bifunctionalized heteroaromatic compound meticulously manufactured for demanding applications in medicinal chemistry and drug development. As a key molecular building block, it provides researchers with a strategic starting point for the efficient synthesis of complex and diverse chemical entities.

    Key Features & Benefits:

    Dual Halogen Functionality: The presence of both bromine and iodine atoms on the robust indazole scaffold allows for selective and sequential palladium-catalyzed cross-coupling reactions. This enables precise, step-wise diversification of the molecule, a critical capability in Structure-Activity Relationship (SAR) studies.

    Synergistic Reactivity: The iodine at the 3-position is typically more reactive in cross-couplings, allowing for initial functionalization. The bromine at the 6-position can then be used in a subsequent, orthogonal coupling step. This controlled reactivity streamlines the synthesis of complex target molecules.

    High-Purity & Reliability: We ensure every batch meets the highest standards of purity (typically >95% by HPLC), confirmed by rigorous QC protocols including NMR and Mass Spectrometry. This guarantees reliable and reproducible results in your most critical experiments.

    Strategic Application: This building block is ideally suited for constructing focused libraries for high-throughput screening, particularly in the development of targeted therapies such as protein kinase inhibitors, oncology agents, and CNS drugs.

    Ordering Information:

    Available in quantities from milligrams to multi-grams. Contact our sales team for custom synthesis and bulk pricing. Data sheets and COA available upon request.

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