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N-Methylbenzamide is a hydrogen bond donor that participates in the transfer of a proton. It contains an amine group, which is highly reactive and can form hydrogen bonds with other molecules. The thermodynamic stability of N-methylbenzamide is due to the dihedral angle between the amine group and carbonyl group. This molecule has been shown to undergo asymmetric synthesis, which allows for the creation of enantiomers. N-Methylbenzamide has been used as a chiral auxiliary in chromatographic science to separate amino acids by using different solvents. N-Methylbenzamide has also been shown to react with sodium carbonate and water molecules, leading to the formation of an amide bond.
Chemical properties
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