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Structure of 50508-60-6
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2-Amino-3-(2-chlorobenzoyl)-5-ethylthiophene features a thiophene core functionalized with an electron-deficient benzoyl group and a pendant ethylthio substituent, enabling integration into bioactive heterocyclic scaffolds. This bench-stable compound facilitates synthesis of kinase inhibitors and fluorescent probes through its reactive amino and carbonyl sites.
2-Amino-3-(2-chlorobenzoyl)-5-ethylthiophene serves as a versatile building block for the synthesis of biologically relevant thiophene derivatives. Its structure features an amino group at C2, a 2-chlorobenzoyl moiety at C3, and an ethylthiophene scaffold, enabling diverse functionalization. The molecule exhibits good bench stability and facilitates straightforward purification, making it suitable for use in medicinal chemistry campaigns targeting kinase inhibitors and other heterocyclic pharmaceuticals.
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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: