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Structure of 942589-45-9
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Methyl 3-amino-5-iodothiophene-2-carboxylate hydrochloride features a bench-stable, electron-rich thiophene core bearing strategically positioned amino and iodo groups. This reactivity-enhanced scaffold enables efficient coupling in transition-metal-catalyzed transformations, serving as a key building block for functionalized heterocycles in medicinal chemistry and materials science applications.
Methyl 3-amino-5-iodothiophene-2-carboxylate hydrochloride serves as a versatile building block for the synthesis of biologically active thiophene derivatives. The amino and iodo groups enable efficient late-stage functionalization via cross-coupling and electrophilic substitution, while the methyl ester supports further derivatization. Bench-stable and compatible with standard reaction conditions, it facilitates rapid access to diversified heterocyclic scaffolds in medicinal chemistry and materials science applications.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: