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Atomfair CID 2736243 C5H3BrClF3O2

Description CID 2736243 (5-bromo-4-chloro-4,5,5-trifluoropent-2-enoic acid) is a highly specialized halogenated organic compound with the molecular formula C5H3BrClF3O2. This chemical is characterized by its unique trifluorinated alkene backbone, coupled with bromo and chloro substituents, making it a valuable intermediate for synthetic organic and medicinal chemistry applications. Its CAS number, 232602-80-1 , ensures precise identification for procurement and regulatory compliance. With a purity grade suitable for research and industrial use, this compound is ideal for advanced chemical synthesis, pharmaceutical development, and material science studies. Proper handling under controlled conditions is recommended due to its reactive functional groups.

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Description

Description

CID 2736243 (5-bromo-4-chloro-4,5,5-trifluoropent-2-enoic acid) is a highly specialized halogenated organic compound with the molecular formula C5H3BrClF3O2. This chemical is characterized by its unique trifluorinated alkene backbone, coupled with bromo and chloro substituents, making it a valuable intermediate for synthetic organic and medicinal chemistry applications. Its CAS number, 232602-80-1, ensures precise identification for procurement and regulatory compliance. With a purity grade suitable for research and industrial use, this compound is ideal for advanced chemical synthesis, pharmaceutical development, and material science studies. Proper handling under controlled conditions is recommended due to its reactive functional groups.

  • CAS No: 232602-80-1
  • Molecular Formula: C5H3BrClF3O2
  • Molecular Weight: 267.43
  • Exact Mass: 265.89570
  • Monoisotopic Mass: 265.89570
  • IUPAC Name: 5-bromo-4-chloro-4,5,5-trifluoropent-2-enoic acid
  • SMILES: C(=CC(C(F)(F)Br)(F)Cl)C(=O)O
  • Synonyms: DNFYVWJPGXJDRN-UHFFFAOYSA-N, CID 2736243

Application

CID 2736243 is primarily utilized as a versatile building block in the synthesis of fluorinated organic compounds, particularly in pharmaceutical and agrochemical research. Its reactive alkene and carboxylic acid functionalities enable participation in cross-coupling reactions, nucleophilic substitutions, and cyclization processes. Researchers value this compound for developing novel bioactive molecules with enhanced metabolic stability due to its trifluoromethyl group. It may also serve as a precursor for specialty polymers or ligands in catalysis.

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