CAS 36640-41-2

3-(4-bromophenyl)-1-phenyl-1H-pyrazole-4-carbaldehyde

Description:

3-(4-Bromophenyl)-1-phenyl-1H-pyrazole-4-carbaldehyde is an organic compound characterized by its pyrazole core, which is a five-membered ring containing two nitrogen atoms. This compound features a phenyl group and a bromophenyl substituent, contributing to its aromatic properties and potential reactivity. The presence of the aldehyde functional group (-CHO) at the 4-position of the pyrazole ring indicates that it can participate in various chemical reactions, such as nucleophilic addition or condensation reactions. The bromine atom in the para position of the phenyl ring enhances the compound's electrophilicity and may influence its biological activity. This compound is of interest in medicinal chemistry and material science due to its potential applications in drug development and as a building block for more complex molecules. Its solubility and stability can vary depending on the solvent and conditions, making it essential to consider these factors in practical applications. Overall, this compound exemplifies the diverse chemistry associated with substituted pyrazoles.

Formula: C₁₆H₁₁BrN₂O

InChI: InChI=1/C16H11BrN2O/c17-14-8-6-12(7-9-14)16-13(11-20)10-19(18-16)15-4-2-1-3-5-15/h1-11H

SMILES: c1ccc(cc1)n1cc(C=O)c(c2ccc(cc2)Br)n1

Synonyms:

• 1H-Pyrazole-4-carboxaldehyde, 3-(4-bromophenyl)-1-phenyl-
• 3-(4-Bromo-phenyl)-1-phenyl-1H-pyrazole-4-carbaldehyde
• 3-(4-Bromophenyl)-1-phenyl-1H-pyrazole-4-carbaldehyde

1H-Pyrazole-4-carboxaldehyde,3-(4-bromophenyl)-1-phenyl-

CAS: 36640-41-2

Formula: C₁₆H₁₁BrN₂O

Purity: 95%

Molecular weight: 327.1753

Ref: IN-DA0078SO

3-(4-Bromophenyl)-1-phenyl-1H-pyrazole-4-carboxaldehyde

CAS: 36640-41-2

Purity: 95.0%

Molecular weight: 327.1809997558594

Ref: 10-F033614

3-(4-Bromophenyl)-1-phenylpyrazole-4-carbaldehyde

CAS: 36640-41-2

3-(4-Bromophenyl)-1-phenylpyrazole-4-carbaldehyde (3BPPA) is an antitubercular agent that belongs to the group of aryl pyrazoles. It is synthesized by reacting 3-bromoaniline with acetaldehyde, followed by condensation with phenylhydrazine, and subsequent cyclization with sodium hydroxide in ethanol. 3BPPA has antitubercular activity and additionally shows some anti-inflammatory properties. The molecule has a pyrazole ring, which is five membered heterocycle containing two nitrogen atoms in the ring. The pharmacological effects of 3BPPA are mediated through its interaction with protein kinase C and inhibition of cell migration. The orientation of the carbaldehyde group is important for the desired pharmacological effects. The azomethine group on 3BPPA can be oriented either cis or trans to the carbaldehyde group, depending on whether it is attached to the same or

Formula: C₁₆H₁₁BrN₂O

Purity: Min. 95%

Molecular weight: 327.18 g/mol

Ref: 3D-FB54028