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CS-W001157 4
Total: USD 88.00

2-Bromo-5-methylthiazole-4-carboxylic acid

  • CAS No. 1194374-25-8

  • Cat. No. CS-W021622
  • Purity≥97%
  • MDL No.MFCD12404925

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

2-Bromo-5-methylthiazole-4-carboxylic acid|CS-W021622

Structure of 1194374-25-8

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General Information

  • CAS No. 1194374-25-8
  • Cat. No. CS-W021622
  • Purity ≥97%
  • MDL No. MFCD12404925
  • Storage -20°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₅H₄BrNO₂S
  • Molecular Weight 222.06
  • Synonym(s) 2-bromo-5-methyl-1,3-thiazole-4-carboxylic acid
  • SMILES O=C(C1=C(C)SC(Br)=N1)O

Description

2-Bromo-5-methylthiazole-4-carboxylic acid features a brominated thiazole core with a methyl group at the 5-position and a carboxylic acid at the 4-position, enabling direct coupling in synthetic routes. This electron-deficient heterocycle integrates readily into bioactive scaffolds, offering enhanced reactivity for C–C and C–heteroatom bond formation under standard conditions.

Application

2-Bromo-5-methylthiazole-4-carboxylic acid serves as a versatile building block in heterocyclic synthesis, enabling efficient access to thiazole-based scaffolds prevalent in medicinal chemistry. Its bromine and carboxylic acid functionalities support diverse transformations, including palladium-catalyzed cross-couplings and derivatization via amide or ester formation. The molecule exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis campaigns and API intermediate development.

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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   50.19
  • LogP   1.91222
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   1

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