Atomfair Benzene, 2-fluoro-4-methyl-1-nitro- C7H6FNO2

Description 2-Fluoro-4-methyl-1-nitrobenzene (CAS No. 446-34-4) is a high-purity nitroaromatic compound with the molecular formula C7H6FNO2. This yellow crystalline solid is a valuable intermediate in organic synthesis, particularly in pharmaceutical and agrochemical research. With a molecular weight of 155.13 g/mol, it features a fluorine substituent at the 2-position and a nitro group at the 1-position of the benzene ring, offering unique reactivity for electrophilic aromatic substitution and nucleophilic displacement reactions. Our product is rigorously tested to ensure ??98% purity (GC) and is supplied in sealed glass containers under inert gas to prevent degradation. Ideal for Suzuki couplings, reduction to anilines, or…

Description

2-Fluoro-4-methyl-1-nitrobenzene (CAS No. 446-34-4) is a high-purity nitroaromatic compound with the molecular formula C₇H₆FNO₂. This yellow crystalline solid is a valuable intermediate in organic synthesis, particularly in pharmaceutical and agrochemical research. With a molecular weight of 155.13 g/mol, it features a fluorine substituent at the 2-position and a nitro group at the 1-position of the benzene ring, offering unique reactivity for electrophilic aromatic substitution and nucleophilic displacement reactions. Our product is rigorously tested to ensure ??98% purity (GC) and is supplied in sealed glass containers under inert gas to prevent degradation. Ideal for Suzuki couplings, reduction to anilines, or as a precursor for fluorinated heterocycles.

CAS No: 446-34-4
Molecular Formula: C7H6FNO2
Molecular Weight: 155.13
Exact Mass: 155.03825660
Monoisotopic Mass: 155.03825660
IUPAC Name: 2-fluoro-4-methyl-1-nitrobenzene
SMILES: CC1=CC(=C(C=C1)[N+](=O)[O-])F
Synonyms: 3-Fluoro-4-nitrotoluene, 446-34-4, 2-Fluoro-4-methyl-1-nitrobenzene, Benzene, 2-fluoro-4-methyl-1-nitro-, gamma-Cyclodextrin, 2-hydroxypropyl ethers

Application

2-Fluoro-4-methyl-1-nitrobenzene serves as a key building block in medicinal chemistry for developing fluorinated drug candidates. The compound’s nitro group facilitates reduction to amino derivatives for aniline-based syntheses, while the fluorine atom enables selective functionalization. Researchers utilize it in palladium-catalyzed cross-coupling reactions to construct biaryl systems common in kinase inhibitors. Its electron-withdrawing properties make it valuable for studying charge-transfer complexes in materials science.

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