CAS 40236-19-9
:Benzyl 3,5-dimethyl-1H-pyrrole-2-carboxylate
Description:
Benzyl 3,5-dimethyl-1H-pyrrole-2-carboxylate is an organic compound characterized by its pyrrole ring structure, which is a five-membered aromatic heterocycle containing nitrogen. The presence of the benzyl group indicates that it has a phenyl ring attached to a methylene (-CH2-) group, enhancing its hydrophobic properties. The 3,5-dimethyl substituents on the pyrrole ring contribute to its steric bulk and influence its reactivity and solubility. As a carboxylate ester, it features a carboxylic acid derivative, which can participate in various chemical reactions, such as hydrolysis or transesterification. This compound may exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its molecular structure suggests potential applications in organic synthesis and as an intermediate in the production of more complex molecules. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper laboratory practices.
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Benzyl 3,5-dimethylpyrrole-2-carboxylate
CAS:Controlled Product<p>Benzyl 3,5-dimethylpyrrole-2-carboxylate is an enol ether that is stabilized by hydrogen bonds. This compound has a polymeric structure and forms dimers and dimers. The chains of the molecule are stabilized by hydrogen bonds. It has a carbonyl group and a carbonyl group that form hydrogen bonds with each other. There are also hydrogen bonding interactions between the benzyl chain and the acetyl groups present in the molecule. Benzyl 3,5-dimethylpyrrole-2-carboxylate is a part of the class of compounds known as polymeric ketones or polyketones, which are characterized by their chains of repeating units.</p>Formula:C14H15NO2Purity:Min. 95%Molecular weight:229.27 g/mol
