Atomfair 2,6-Difluoro-3-nitrobenzaldehyde C7H3F2NO3 CAS 606966-11-4

2,6-Difluoro-3-nitrobenzaldehyde (CAS No. 606966-11-4) is a high-purity, fluorinated aromatic aldehyde with the molecular formula C7H3F2NO3. This compound is characterized by its two fluorine substituents and a nitro group at the meta position relative to the aldehyde functionality, making it a versatile building block for organic synthesis and pharmaceutical research. It is supplied as a crystalline solid with a purity of ≥98% (HPLC) and is ideal for use in nucleophilic substitution reactions, cross-coupling reactions, and as a precursor for heterocyclic compounds. Proper storage conditions (2-8°C, under inert atmosphere) ensure long-term stability. Available in packaging options ranging from 1g to 100g, this…

Description

2,6-Difluoro-3-nitrobenzaldehyde (CAS No. 606966-11-4) is a high-purity, fluorinated aromatic aldehyde with the molecular formula C7H3F2NO3. This compound is characterized by its two fluorine substituents and a nitro group at the meta position relative to the aldehyde functionality, making it a versatile building block for organic synthesis and pharmaceutical research. It is supplied as a crystalline solid with a purity of ≥98% (HPLC) and is ideal for use in nucleophilic substitution reactions, cross-coupling reactions, and as a precursor for heterocyclic compounds. Proper storage conditions (2-8°C, under inert atmosphere) ensure long-term stability. Available in packaging options ranging from 1g to 100g, this product is tailored for researchers requiring precise and reliable reagents.

Properties

  • CAS Number: 606966-11-4
  • Complexity: 218
  • IUPAC Name: 2,6-difluoro-3-nitro-benzaldehyde
  • InChI: InChI=1S/C7H3F2NO3/c8-5-1-2-6(10(12)13)7(9)4(5)3-11/h1-3H
  • InChI Key: KFAXVNHRKYGPED-UHFFFAOYSA-N
  • Exact Mass: 187.00809928
  • Molecular Formula: C7H3F2NO3
  • Molecular Weight: 187.10
  • SMILES: C1=CC(=C(C(=C1[N+](=O)[O-])F)C=O)F
  • Topological: 62.9
  • Monoisotopic Mass: 187.00809928
  • Synonyms: 2,6-Difluoro-3-nitrobenzaldehyde, 606966-11-4, MFCD16877510, 2,6-Difluoro-3-nitro-benzaldehyde, Benzaldehyde, 2,6-difluoro-3-nitro-, SCHEMBL285844, SCHEMBL285845, DTXSID60569986, KFAXVNHRKYGPED-UHFFFAOYSA-N, GZA96611, ZB1096, AKOS027384279, FS-4401, SY365093, DB-292332, CS-0105558, EN300-97372, D76553, Z1255500933

Application

2,6-Difluoro-3-nitrobenzaldehyde is widely used as a key intermediate in the synthesis of agrochemicals, pharmaceuticals, and specialty materials. Its electron-withdrawing groups (fluoro and nitro) enhance reactivity in Suzuki-Miyaura and Buchwald-Hartwig couplings, facilitating the construction of complex aromatic systems. Researchers also employ it in the development of fluorinated dyes and ligands for catalysis. Its structural features make it valuable for probing electronic effects in medicinal chemistry.

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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.

Disclaimer

Intended Use & Restrictions

This product is sold exclusively for laboratory research, analytical testing, or non-commercial purposes.

  • Strictly prohibited: Resale, repackaging, or formulation into commercial products.
  • Not approved for human/animal use, diagnostics, or manufacturing (including pharmaceuticals, agrochemicals, or consumer goods).

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