Atomfair 1-(Bromodifluoromethyl)cyclohex-1-ene C7H9BrF2

Description 1-(Bromodifluoromethyl)cyclohex-1-ene (CAS No. 117711-60-1) is a highly specialized organobromine compound with the molecular formula C7H9BrF2. This chemical is characterized by its unique bromodifluoromethyl functional group attached to a cyclohexene ring, making it a valuable intermediate in synthetic organic chemistry. It is particularly useful in nucleophilic substitution reactions , cross-coupling reactions , and as a building block for the synthesis of fluorinated organic compounds. The compound is supplied as a high-purity liquid, rigorously tested for consistency and quality, ensuring optimal performance in research and industrial applications. Proper storage under inert conditions is recommended to maintain stability.

Description

1-(Bromodifluoromethyl)cyclohex-1-ene (CAS No. 117711-60-1) is a highly specialized organobromine compound with the molecular formula C₇H₉BrF₂. This chemical is characterized by its unique bromodifluoromethyl functional group attached to a cyclohexene ring, making it a valuable intermediate in synthetic organic chemistry. It is particularly useful in nucleophilic substitution reactions, cross-coupling reactions, and as a building block for the synthesis of fluorinated organic compounds. The compound is supplied as a high-purity liquid, rigorously tested for consistency and quality, ensuring optimal performance in research and industrial applications. Proper storage under inert conditions is recommended to maintain stability.

CAS No: 117711-60-1
Molecular Formula: C7H9BrF2
Molecular Weight: 211.05
Exact Mass: 209.98557
Monoisotopic Mass: 209.98557
IUPAC Name: 1-[bromo(difluoro)methyl]cyclohexene
SMILES: C1CCC(=CC1)C(F)(F)Br
Synonyms: 117711-60-1, 1-(Bromodifluoromethyl)cyclohex-1-ene, 1-(Bromodifluoromethyl)cyclohexene, 1-[bromo(difluoro)methyl]cyclohexene, Cyclohexene, 1-(bromodifluoromethyl)-

Application

1-(Bromodifluoromethyl)cyclohex-1-ene is widely employed in pharmaceutical research and agrochemical development as a key fluorinated synthon. Its reactivity enables the introduction of difluoromethyl groups into complex molecules, enhancing their biological activity or metabolic stability. Researchers also utilize this compound in material science for designing novel fluorinated polymers with unique properties. Its versatility makes it indispensable in advanced synthetic methodologies.

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