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Structure of 1001907-23-8
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Tert-butyl 5-iodo-1H-indazole-1-carboxylate features a bench-stable indazole core functionalized with a reactive iodide at the 5-position, enabling efficient cross-coupling transformations. The tert-butyl ester group provides solubility and stability under standard conditions, simplifying purification and handling in synthetic workflows. This compound serves as a key intermediate for constructing complex heterocyclic architectures in medicinal chemistry and materials science applications.
Tert-butyl 5-iodo-1H-indazole-1-carboxylate serves as a versatile building block for the synthesis of indazole-based scaffolds in medicinal chemistry. The iodine substituent enables reliable cross-coupling reactions, including Suzuki-Miyaura and Stille couplings, while the tert-butyl ester offers stability and convenient deprotection under mild acidic conditions. This compound exhibits excellent bench stability and functional group tolerance, facilitating efficient access to complex heterocyclic architectures in drug discovery campaigns.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: