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CS-W001157 4
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2-(3-Bromophenyl)thiazole-4-carboxylic acid

  • CAS No. 886369-02-4

  • Cat. No. CS-0040695
  • Molecule weightNone
  • Purity≥98%
  • MDL No.MFCD07375292

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

2-(3-Bromophenyl)thiazole-4-carboxylic acid|CS-0040695

Structure of 886369-02-4

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General Information

  • CAS No. 886369-02-4
  • Cat. No. CS-0040695
  • Purity ≥98%
  • MDL No. MFCD07375292
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₆BrNO₂S
  • Molecular Weight None
  • Synonym(s) 2-(3-BROMO-PHENYL)-THIAZOLE-4-CARBOXYLIC ACID
  • SMILES O=C(C1=CSC(C2=CC=CC(Br)=C2)=N1)O

Description

2-(3-Bromophenyl)thiazole-4-carboxylic acid features a brominated phenyl ring fused to a thiazole core, delivering enhanced electron-withdrawing character and improved solubility in polar solvents. This scaffold enables direct incorporation into bioactive molecules, particularly in kinase inhibitors and pharmaceutical intermediates. The carboxylic acid group facilitates coupling reactions under standard amide formation conditions.

Application

2-(3-Bromophenyl)thiazole-4-carboxylic acid serves as a versatile building block for the synthesis of biologically relevant heterocycles and pharmaceutical intermediates. Its structure combines a brominated phenyl group with a thiazole carboxylic acid moiety, enabling facile Suzuki-Miyaura and other Pd-catalyzed couplings. The carboxylic acid functionality offers direct access to amides, esters, and other derivatives, facilitating downstream functionalization in medicinal chemistry campaigns. The compound exhibits good bench stability and is readily purified by recrystallization or chromatography.

Safety Information

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Computational Chemistry Data

  • TPSA   50.19
  • LogP   3.2708
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   2

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