AC-36721 - 5-bromo-2-hydroxyacetophenone-98 | 1450-75-5
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Ethanone, 1-(5-bromo-2-hydroxyphenyl)-
CAS:Formula:C8H7BrO2Purity:98%Color and Shape:SolidMolecular weight:215.04405'-Bromo-2'-hydroxyacetophenone
CAS:Formula:C8H7BrO2Purity:>97.0%(GC)Color and Shape:White to Yellow to Orange powder to crystalMolecular weight:215.055'-Bromo-2'-hydroxyacetophenone, 98%
CAS:5?-Bromo-2?-hydroxyacetophenone (5-Bromo-2-hydroxyacetophenone) may be used in ligand in the preparation of tetrahedral metallocene complexes containing vanadium(IV), synthesis of {2?-[1-(5-bromo-2-oxidophenyl) ethylidene] benzohydrazidato (2-)} tris(pyridine) nickel(II)] pyridine solvate, synthesis
Formula:C8H7BrO2Purity:98%Molecular weight:215.055'-Bromo-2'-hydroxyacetophenone
CAS:5'-Bromo-2'-hydroxyacetophenoneFormula:C8H7BrO2Purity:≥95%Color and Shape: light yellow solidMolecular weight:215.04g/mol5′-Bromo-2′-hydroxyacetophenone
CAS:Formula:C8H7BrO2Purity:98%Color and Shape:CrystallineMolecular weight:215.0461-(5-Bromo-2-hydroxyphenyl)ethanone
CAS:Controlled ProductApplications 1-(5-Bromo-2-hydroxyphenyl)ethanone
Formula:C8H7BrO2Color and Shape:NeatMolecular weight:215.0445'-Bromo-2'-hydroxyacetophenone
CAS:5'-Bromo-2'-hydroxyacetophenone is a chemical that is used as a substrate in the preparation of other chemicals. The reaction solution contains 5'-bromo-2'-hydroxyacetophenone, nitrogen atoms, and a biological sample. This substrate reacts with trifluoroacetic acid to form an intramolecular hydrogen bond. The magnetic resonance spectrum of this product reveals the presence of two carbon atoms, three hydrogen atoms, and one oxygen atom. The resulting chemical structure is that of 2-Aminobenzamide.Formula:C8H7BrO2Purity:Min. 95%Color and Shape:White PowderMolecular weight:215.04 g/mol
