Bowroju, Suresh Kuarm team published research on Russian Journal of Bioorganic Chemistry in 2021 | 90-59-5

Recommanded Product: 3,5-Dibromo-2-hydroxybenzaldehyde, 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.

Vinyl bromides undergo the Heck reaction, which involves C-C coupling with alkene to give substituted alkenes. 90-59-5, formula is C7H4Br2O2, Name is 3,5-Dibromo-2-hydroxybenzaldehyde. Methyl bromide is a precursor in the manufacture of several chemicals and is employed as a soil sterilant, mainly for seed production. Recommanded Product: 3,5-Dibromo-2-hydroxybenzaldehyde.

Bowroju, Suresh Kuarm;Marumamula, Hanumaiah;Bavanthula, Rajitha research published 《 Design and Synthesis of 11H-Xantheno[2,1-c][1,2,5]Selenadiazol-11-One Derivatives as Potent Antimicrobial and Antitubercular Agents》, the research content is summarized as follows. A series of 11H-xantheno[2,1-c][1,2,5]selenadiazol-11-one derivatives I (R = H; R1 = H, Me, Cl, Br, etc.; R2 = H, OMe, F, NO2, etc.; RR2 = -(CH=CHCH=CH)-) that incorporate a variety of substituents have been synthesized under both conventional heating and microwave irradiation procedures. All these analogs I were evaluated for their antimicrobial activity against the Gram-pos. bacteria Bacillus subtilis (BS), Staphylococcus aureus (SA), and Staphylococcus epidermidis (SE), against the Gram-neg. bacteria Escherichia coli (EC), Pseudomonas aeruginosa (PA), and Klebsiella pneumonia (KP), and against the fungal species Candida albicans (CA), Candida rugosa (CR), Rhizopus oryzae (RO), and Aspergillus niger (AN) and antitubercular activity against MTB H37Rv. Analog, I (R = H, R1 = R2 = OMe) (II) was identified as a potent antibacterial agent (MIC[BS] = 2.5μg/mL, MIC[SA] = 10μg/mL, MIC[SE] = 2.5μg/mL, MIC[EC] = 5μg/mL, MIC[PA] = 10μg/mL, MIC[KP] = 2.5μg/mL), and a potent antifungal agent (MIC[CA] = 15μg/mL, MIC[CR] = 15μg/mL, MIC[RO] = 10μg/mL). Another analog, I (R = H, R1 = R2 = Me) (III) was also identified as a potent antibacterial agent (MIC[BS] = 2.5μg/mL, MIC[SA] = 15μg/mL, MIC[SE] = 2.5μg/mL, MIC[EC] = 10μg/mL, MIC[PA] = 15μg/mL, MIC[KP] = 20μg/mL), and a potent antifungal agent (MIC[CA] = 2.5 g/mL, MIC[CR] = 10μg/mL MIC[RO] = 15μg/mL and MIC[AN] = 10μg/mL). Based on the MIC data analogs, II and III were identified as the most potent antimicrobial agents in the series. All these 11H-xantheno[2,1-c][1,2,5]selenadiazol-11-one derivatives I were also evaluated for their antitubercular activity against MTB H37Rv. Analogs, II and III showed MIC of 3.12μg/mL. These results suggest that analogs, II and III may be potential multifunctional ligands for the development of highly effective antimicrobial and antitubercular activity.

Recommanded Product: 3,5-Dibromo-2-hydroxybenzaldehyde, 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