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5-tert-Butyl 3-ethyl 2-amino-4H,5H,6H,7H-thieno[3,2-c]pyridine-3,5-dicarboxylate

  • CAS No. 1101856-88-5

  • Cat. No. CS-0050406
  • Molecule weight326.41
  • Purity≥97%
  • MDL No.None

*For research and further manufacturing use only, not for direct human use.

5-tert-Butyl 3-ethyl 2-amino-4H,5H,6H,7H-thieno[3,2-c]pyridine-3,5-dicarboxylate|CS-0050406

Structure of 1101856-88-5

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General Information

  • CAS No. 1101856-88-5
  • Cat. No. CS-0050406
  • Purity ≥97%
  • MDL No. None
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₅H₂₂N₂O₄S
  • Molecular Weight 326.41
  • Synonym(s) 5-tert-butyl 3-ethyl 2-amino-6,7-dihydrothieno[3,2-c]pyridine-3,5(4H)-dicarboxylate
  • SMILES CCOC(=O)C1=C(N)SC2=C1CN(CC2)C(=O)OC(C)(C)C

Description

5-tert-Butyl 3-ethyl 2-amino-4H,5H,6H,7H-thieno[3,2-c]pyridine-3,5-dicarboxylate features a sterically shielded tert-butyl group and an electron-rich amino function, enabling robust coupling in late-stage functionalization. The fused thienopyridine core provides planarity and enhanced stability under standard bench conditions. This scaffold integrates readily into bioactive molecule synthesis.

Application

5-tert-Butyl 3-ethyl 2-amino-4H,5H,6H,7H-thieno[3,2-c]pyridine-3,5-dicarboxylate serves as a versatile heterocyclic building block for medicinal chemistry and materials science. Its amino and carboxylate functionalities enable facile derivatization via amide coupling, alkylation, and transition-metal-catalyzed cross-coupling reactions. The tert-butyl and ethyl groups enhance solubility and stability, while the thienopyridine core provides a rigid, planar scaffold suitable for structure-activity studies.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   81.86
  • LogP   2.8002
  • H_Acceptors   6
  • H_Donors   1
  • Rotatable_Bonds   2

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