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Structure of 81136-42-7
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4-Chloro-6-ethylthieno[2,3-d]pyrimidine features a fused thienopyrimidine core with strategic halogen and alkyl substitution, enabling direct functionalization in heterocyclic synthesis. The chloro group at the 4-position serves as a reactive handle for palladium-catalyzed cross-coupling, while the ethyl substituent at the 6-position enhances solubility and modulates electronic properties. This scaffold delivers robust performance under standard bench conditions.
4-Chloro-6-ethylthieno[2,3-d]pyrimidine serves as a versatile heterocyclic building block in medicinal chemistry, enabling efficient access to purine and pyrimidine analogs. The chloro group at C4 facilitates nucleophilic substitution reactions, while the ethylthienopyrimidine core provides structural rigidity and favorable electronic properties for target-directed synthesis. Its bench-stable nature and compatibility with standard coupling protocols make it ideal for modular library construction and API intermediate development.
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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: