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Atomfair 2-Fluorocinnamaldehyde C9H7FO

Description 2-Fluorocinnamaldehyde (CAS No. 149733-71-1) is a high-purity fluorinated aromatic aldehyde with the molecular formula C9H7FO. This compound, also known by its IUPAC name (E)-3-(2-fluorophenyl)prop-2-enal, is a valuable building block in organic synthesis and pharmaceutical research. The presence of both a fluorine substituent and an ??,??-unsaturated aldehyde moiety makes it particularly useful for nucleophilic additions and cyclization reactions. Our product is rigorously tested to ensure >98% purity by HPLC, with detailed analytical data (NMR, MS) available upon request. Supplied in amber glass vials under inert atmosphere to ensure stability, this reagent is ideal for use in medicinal chemistry, material science,…

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Description

Description

2-Fluorocinnamaldehyde (CAS No. 149733-71-1) is a high-purity fluorinated aromatic aldehyde with the molecular formula C9H7FO. This compound, also known by its IUPAC name (E)-3-(2-fluorophenyl)prop-2-enal, is a valuable building block in organic synthesis and pharmaceutical research. The presence of both a fluorine substituent and an ??,??-unsaturated aldehyde moiety makes it particularly useful for nucleophilic additions and cyclization reactions. Our product is rigorously tested to ensure >98% purity by HPLC, with detailed analytical data (NMR, MS) available upon request. Supplied in amber glass vials under inert atmosphere to ensure stability, this reagent is ideal for use in medicinal chemistry, material science, and as a precursor for fluorinated heterocycles.

  • CAS No: 149733-71-1
  • Molecular Formula: C9H7FO
  • Molecular Weight: 150.15
  • Exact Mass: 150.048093005
  • Monoisotopic Mass: 150.048093005
  • IUPAC Name: (E)-3-(2-fluorophenyl)prop-2-enal
  • SMILES: C1=CC=C(C(=C1)/C=C/C=O)F
  • Synonyms: 2-FLUOROCINNAMALDEHYDE, 149733-71-1, (E)-3-(2-Fluorophenyl)acrylaldehyde, 2-Propenal, 3-(2-fluorophenyl)-, (2E)-, (E)-3-(2-fluorophenyl)prop-2-enal

Application

2-Fluorocinnamaldehyde serves as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals. It is particularly valuable in the preparation of chalcone derivatives with potential biological activity. The compound’s reactive aldehyde group allows for facile derivatization through condensation or addition reactions. Researchers utilize this chemical in the development of novel fluorinated materials with enhanced electronic properties.

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