Description

1-Bromo-4-butoxy-2,3-difluorobenzene (CAS No. 247176-22-3) is a high-purity halogenated aromatic compound with the molecular formula C₁₀H₁₁BrF₂O. This specialized chemical features a bromine substituent at the 1-position and a butoxy group at the 4-position, along with two fluorine atoms at the 2- and 3-positions on the benzene ring, making it a valuable intermediate in synthetic organic chemistry. Its unique structure is ideal for nucleophilic substitution reactions, cross-coupling reactions (e.g., Suzuki-Miyaura, Buchwald-Hartwig), and as a building block for advanced materials. Available in >97% purity (HPLC/GC), this compound is supplied in rigorously tested batches with detailed analytical certificates (COA). Suitable for pharmaceutical research, agrochemical development, and liquid crystal synthesis. Store under inert atmosphere at 2-8°C to maintain stability.

Properties

• CAS Number: 247176-22-3
• Complexity: 168
• IUPAC Name: 1-bromo-4-butoxy-2,3-difluoro-benzene
• InChI: InChI=1S/C10H11BrF2O/c1-2-3-6-14-8-5-4-7(11)9(12)10(8)13/h4-5H,2-3,6H2,1H3
• InChI Key: VZOZRBSBWHDDHS-UHFFFAOYSA-N
• Exact Mass: 263.99613
• Molecular Formula: C10H11BrF2O
• Molecular Weight: 265.09
• SMILES: CCCCOC1=C(C(=C(C=C1)Br)F)F
• Topological: 9.2
• Monoisotopic Mass: 263.99613
• Synonyms: 1-Bromo-4-butoxy-2,3-difluorobenzene, 247176-22-3, Benzene, 1-bromo-4-butoxy-2,3-difluoro-, 4-Butoxy-2,3-difluorobromobenzene, C10H11BrF2O, MFCD07368020, SCHEMBL7911521, DTXSID70591076, SBB102885, AKOS015961670, 1-bromo-4-butoxy-2,3-difluoro-benzene, AC-14518, AS-64310, CS-0323881

Application

1-Bromo-4-butoxy-2,3-difluorobenzene serves as a versatile precursor in the synthesis of liquid crystal materials for display technologies due to its fluorinated aromatic core. It is employed in pharmaceutical research for constructing drug candidates with enhanced metabolic stability via its bromine moiety. The compound also finds use in agrochemical synthesis as a key intermediate for crop protection agents. Its electron-deficient benzene ring facilitates palladium-catalyzed cross-coupling reactions in materials science applications.

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