CAS 19227-14-6

4-BROMO-N'-HYDROXYBENZENECARBOXIMIDAMIDE

Description:

4-Bromo-N'-hydroxybenzenecarboximidamide is a chemical compound characterized by its unique structure, which includes a bromine atom, a hydroxyl group, and an amidine functional group. The presence of the bromine atom introduces notable reactivity and can influence the compound's biological activity. The hydroxyl group contributes to the compound's potential solubility in polar solvents and may participate in hydrogen bonding, enhancing its interactions with other molecules. The amidine functional group is known for its basicity and can act as a nucleophile in various chemical reactions. This compound may exhibit biological properties, making it of interest in pharmaceutical research, particularly in the development of new therapeutic agents. Its CAS number, 19227-14-6, allows for easy identification in chemical databases. Overall, 4-bromo-N'-hydroxybenzenecarboximidamide is a versatile compound with potential applications in medicinal chemistry and organic synthesis, although specific applications would depend on further research into its properties and reactivity.

Formula: C₆H₅FN₂O₂

InChI: InChI=1/C6H5FN2O2/c1-4-2-3-5(9(10)11)6(7)8-4/h2-3H,1H3

SMILES: Cc1ccc(c(F)n1)N(=O)=O

Synonyms:

• 4-Bromobenzamidoxime
• P-Bromobenzamidoxim,4-Bromo-N-Hydroxy-Benzamidine
• (E)-4-Bromo-N'-hydroxybenzimidamide
• P-Bromobenzamidoxime
• 2-Fluoro-6-Methyl-3-Nitro-Pyridine

(E)-4-Bromo-N'-hydroxybenzimidamide

CAS: 19227-14-6

Formula: C₇H₇BrN₂O

Purity: 98%

Color and Shape: Solid

Molecular weight: 215.0473

Ref: IN-DA002FSI

4-Bromobenzamidoxime

CAS: 19227-14-6

4-Bromobenzamidoxime

Formula: C₇H₇BrN₂O

Purity: ≥95%

Color and Shape: white solid

Molecular weight: 215.05g/mol

Ref: 54-OR14239

4-Bromobenzamidoxime

CAS: 19227-14-6

Formula: C₇H₇BrN₂O

Purity: 98%

Color and Shape: Solid

Molecular weight: 215.05

Ref: 10-F021899

(E)-4-Bromo-N'-hydroxybenzimidamide

CAS: 19227-14-6

(E)-4-Bromo-N'-hydroxybenzimidamide is a synthetic antifungal agent that is resistant to many microorganisms. It is a potent inhibitor of the uptake of β-amyloid peptide in rat cortical neurons and also inhibits the modification of β-amyloid. This drug has been shown to have pharmacological effects on bacterial cells, including inhibition of protein synthesis and DNA synthesis. The molecular basis for these interactions is not known, but it has been suggested that (E)-4-Bromo-N'-hydroxybenzimidamide interacts with the pharmacophore site on bacteria and binds to nitrogen atoms that are important for binding. These interactions are bioisosteric with oxadiazole derivatives such as clotrimazole, which have been shown to inhibit protein synthesis in fungi. The drug has also been used as a radiotracer to study the uptake of β-amyloid peptides by neurons

Formula: C₇H₇BrN₂O

Purity: Min. 95%

Molecular weight: 215.05 g/mol

Ref: 3D-UAA22714