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Structure of 18774-47-5
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2-Aminobenzo[b]thiophene-3-carbonitrile features a fused heterocyclic core integrating an electron-rich amine and a strongly polar nitrile group. This combination enables direct participation in cross-coupling reactions and facilitates downstream derivatization in medicinal chemistry. The scaffold exhibits robust stability under standard bench conditions and displays favorable solubility in common organic solvents, supporting its use in synthetic workflows requiring precise functional group handling.
2-Aminobenzo[b]thiophene-3-carbonitrile serves as a versatile heterocyclic building block for medicinal chemistry and materials science. Its ortho-substituted scaffold enables efficient transition-metal-catalyzed coupling reactions, while the amino and nitrile groups offer complementary handles for derivatization. Bench-stable and amenable to purification via recrystallization, it facilitates rapid access to complex fused-ring architectures relevant to kinase inhibitors and organic semiconductors.
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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: