119924-92-4 | 1-[4-(2-Methylimidazol-1-yl)phenyl]ethanone

Packsize	Purity	Availability	Price	Discounted Price
1g	96%	in stock	$89.00	$62.00
5g	96%	in stock	$249.00	$175.00
10g	96%	in stock	$401.00	$281.00
25g	96%	in stock	$758.00	$531.00

Description

• Catalog Number: AE25261
• Chemical Name: 1-[4-(2-Methylimidazol-1-yl)phenyl]ethanone
• CAS Number: 119924-92-4
• Molecular Formula: C12H12N2O
• Molecular Weight: 200.23647999999997
• MDL Number: MFCD07365186
• SMILES: CC(=O)c1ccc(cc1)n1ccnc1C

Computed Properties

• Complexity: 234
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• XLogP3: 1.8

Upstream Synthesis Route

1-[4-(2-Methylimidazol-1-yl)phenyl]ethanone is a versatile compound widely utilized in chemical synthesis processes. This particular molecule serves as a valuable intermediate in the production of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure, containing both an imidazole ring and a ketone functional group, allows for a wide range of chemical reactions and transformations. For instance, the imidazole moiety enables the compound to participate in nucleophilic substitution reactions, while the ketone group facilitates reactions such as reduction, oxidation, and condensation.In organic synthesis, 1-[4-(2-Methylimidazol-1-yl)phenyl]ethanone can be used as a key building block for the construction of complex molecules. By selectively modifying different parts of its structure, chemists can control the stereochemistry, reactivity, and functionality of the final product. Additionally, this compound's ability to act as a chelating agent makes it valuable in coordination chemistry and metal-catalyzed reactions.Overall, the application of 1-[4-(2-Methylimidazol-1-yl)phenyl]ethanone in chemical synthesis is instrumental in the development of new materials, drugs, and compounds with diverse functionalities and applications. Its strategic placement within synthetic pathways contributes to the efficient and effective production of target molecules in both academic research and industrial settings.