29618-28-8

Basic information

• Product Name: Benzamide, N-[2-methyl-1-[(phenylamino)carbonyl]propyl]-, (S)-
• CAS NO: 29618-28-8
• Molecular Formula: C18H20N2O2
• Molecular Weight: 296.369
• Mol File: 29618-28-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Benzamide, N-[2-methyl-1-[(phenylamino)carbonyl]propyl]-, (S)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, N-[2-methyl-1-[(phenylamino)carbonyl]propyl]-, (S)-(29618-28-8)
• EPA Substance Registry System: Benzamide, N-[2-methyl-1-[(phenylamino)carbonyl]propyl]-, (S)-(29618-28-8)

Safety Data

• Hazardous Substances Data: 29618-28-8(Hazardous Substances Data)

Usage

General Description

Benzamide, N-[2-methyl-1-[(phenylamino)carbonyl]propyl]-, (S)- is a chemical compound that belongs to the benzamide class of compounds. It consists of a benzene ring attached to a carbonyl group and a propyl chain, with a methyl group located at the 2-position of the propyl chain. The (S)- designation indicates that this compound is the S enantiomer, meaning that it has a specific chirality. This chemical may have various uses in pharmaceuticals, research, or other industrial applications due to its unique structure and properties.

Upstream product

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Relevant articles and documents

A study of the strength of a template molecule - A functional monomer interaction that affects the performance of molecularly imprinted polymers and its application to chiral amplification

A novel type of molecularly imprinted polymer (MIP), N-benzoyl-(S)-valine anilide-imprinted polymer (IP-2), was prepared using hydrogen-bonding interactions as a main force in the pre-polymerization step. The performance of the IP-2 was evaluated via batch procedure and compared with a (S)-valine anilideimprinted polymer (IP-1) that was prepared using an ionic interaction that is stronger than hydrogen bonding. Although both polymers showed a preferential adsorbability for (S)-amino acid derivatives, different performances were observed in terms of adsorbability and enantioselectivity. In addition, the IP-2 was able to recognize the enantiomer of a valine-derived chiral catalyst. This phenomenon was applied to a chiral amplification reaction, and a highly selective asymmetric Mannich-type amination was achieved using the combination of a racemic catalyst and a MIP.