Chen, Yue team published research on Dalton Transactions in 2021 | 90-59-5

Application of C7H4Br2O2, 3,5-Dibromosalicylaldehyde reacts with alkyl cyanoacetates in the presence of ammonium acetate to yield 4H- chromenes.

3,5-Dibromosalicylaldehyde, also known as 3,5-Dibromosalicylaldehyde, is a useful research compound. Its molecular formula is C7H4Br2O2 and its molecular weight is 279.91 g/mol. The purity is usually 95%.

3,5-Dibromosalicylaldehyde reacts with alkyl cyanoacetates in the presence of ammonium acetate to yield 4H- chromenes. 3,5-Dibromosalicylaldehyde can be used in the synthesis of Schiff base and can be used as reactant for synthesis of Schiff base ligands which forms mononuclear complexes with copper(II), nickel(II), zinc(II) and cobalt(II).

3,5-Dibromosalicylaldehyde is a copper complex that has been synthesized from 3,5-dibromosalicylaldehyde and copper chloride. FTIR spectroscopy revealed that the coordination geometry of the copper complex is octahedral with two nitrogen atoms in the equatorial plane. The presence of hydrogen bonding interactions was confirmed by homologous protein adsorption experiments. This chemical structure was determined using X-ray crystallography and fluorescence probe experiments. The copper complex showed high affinity for malonic acid, which is an ester hydrochloride. The molecular mechanism of this interaction is based on adsorption, which occurs through hydrogen bonding interactions and hydrophobic interactions. Structural analysis revealed that the polymeric matrix consists of a three-dimensional network of crosslinked chains, while FTIR analysis indicated a possible disulfide bond between two cysteine residues., 90-59-5.

Dehydrobromination, Grignard reactions, reductive coupling, Wittig reaction, and several nucleophilic substitution reactions are some of the principal reactions which involve organic bromides. 90-59-5, formula is C7H4Br2O2, Name is 3,5-Dibromo-2-hydroxybenzaldehyde. Organic compounds having carbon bonded to bromine are called organic bromides. Application of C7H4Br2O2.

Chen, Yue;Yang, Qi;Peng, Guo;Zhang, Yi-Quan;Ren, Xiao-Ming research published 《 Influence of F-position and solvent on coordination geometry and single ion magnet behavior of Co(II) complexes》, the research content is summarized as follows. Three mononuclear Co(II) complexes with the compositions of [Co(L1)2] (1), [Co(L2)2(MeCN)] (2) and [Co(L3)2] (3) (HL1 = 2-((E)-(2-fluorobenzylimino)methyl)-4,6-dibromophenol, HL2 = 2-((E)-(3-fluorobenzylimino)methyl)-4,6-dibromophenol and HL3 = 2-((E)-(4-fluorobenzylimino)methyl)-4,6-dibromophenol) were prepared and structurally determined The changes in the F-positions in the ligands and solvents gave these products with various coordination geometries. Both complexes 1 and 3 are four-coordinated and their coordination geometries can be described as tetrahedron and seesaw, whereas complex 2 is five coordinated with a coordination configuration in between trigonal bipyramid and square pyramid. Static magnetic studies reveal that all these complexes exhibit considerable easy-axis magnetic anisotropy. The easy-axis magnetic anisotropy of 1 and 3 mainly derives from the first quartet excited state, whereas that of 2 primarily originates from the first, third and fourth quartet excited states established by theor. calculations All the resulting complexes display field-induced slow magnetic relaxation. Complex 3 represents the first Co(II) single ion magnet with a seesaw coordination geometry. Ab initio calculations predict that the magnetic anisotropy will enhance when the seesaw coordination geometry varies from distortion to regulation.

Application of C7H4Br2O2, 3,5-Dibromosalicylaldehyde reacts with alkyl cyanoacetates in the presence of ammonium acetate to yield 4H- chromenes.

3,5-Dibromosalicylaldehyde, also known as 3,5-Dibromosalicylaldehyde, is a useful research compound. Its molecular formula is C7H4Br2O2 and its molecular weight is 279.91 g/mol. The purity is usually 95%.

3,5-Dibromosalicylaldehyde reacts with alkyl cyanoacetates in the presence of ammonium acetate to yield 4H- chromenes. 3,5-Dibromosalicylaldehyde can be used in the synthesis of Schiff base and can be used as reactant for synthesis of Schiff base ligands which forms mononuclear complexes with copper(II), nickel(II), zinc(II) and cobalt(II).

3,5-Dibromosalicylaldehyde is a copper complex that has been synthesized from 3,5-dibromosalicylaldehyde and copper chloride. FTIR spectroscopy revealed that the coordination geometry of the copper complex is octahedral with two nitrogen atoms in the equatorial plane. The presence of hydrogen bonding interactions was confirmed by homologous protein adsorption experiments. This chemical structure was determined using X-ray crystallography and fluorescence probe experiments. The copper complex showed high affinity for malonic acid, which is an ester hydrochloride. The molecular mechanism of this interaction is based on adsorption, which occurs through hydrogen bonding interactions and hydrophobic interactions. Structural analysis revealed that the polymeric matrix consists of a three-dimensional network of crosslinked chains, while FTIR analysis indicated a possible disulfide bond between two cysteine residues., 90-59-5.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary