7200-19-3

Usage

Uses

Used in Organic Chemistry:
L-Leucine, N-benzoyl-, ethyl ester is used as a synthetic reagent for the preparation of peptide and protein derivatives. It plays a crucial role in the synthesis of various bioactive compounds and pharmaceuticals.
Used in Pharmaceutical Research and Development:
L-Leucine, N-benzoyl-, ethyl ester is used as a research compound in the development of pharmaceuticals and bioactive compounds. Its unique structure and properties make it a valuable tool in the discovery and optimization of new drug candidates.
Used in Nutritional Supplements:
L-Leucine, N-benzoyl-, ethyl ester is used as a nutritional supplement for athletes and individuals looking to improve their muscle mass and physical performance. It is known for its role in promoting muscle protein synthesis, which can contribute to increased strength and muscle growth.

Upstream product

• 2743-60-4 L-Leucine ethyl ester 
• 83697-67-0 N-benzoyl-(6H)phenanthridine 
• 2743-40-0 L-leucine ethyl ester hydrochloride 
• 100-52-7 benzaldehyde 
• 65-85-0 benzoic acid 

Downstream Products

• 1466-83-7 N-benzoyl-L-leucine 

Relevant academic research and scientific papers

Cross-Dehydrogenating Coupling of Aldehydes with Amines/R-OTBS Ethers by Visible-Light Photoredox Catalysis: Synthesis of Amides, Esters, and Ureas

A straightforward synthesis of amides, ureas, and esters is reported by visible-light cross-dehydrogenating coupling (CDC) of aldehydes (or amine carbaldehydes) and amines/R-OTBS ethers by photoredox catalysis. The reaction is found to be general and high yielding. A plausible mechanistic pathway has been proposed for these transformations and is supported by appropriate controlled experiments.

Optimization of dipeptidic inhibitors of cathepsin L for improved Toxoplasma gondii selectivity and CNS permeability

The neurotropic protozoan Toxoplasma gondii is the second leading cause of death due to foodborne illness in the US, and has been designated as one of five neglected parasitic infections by the Center for Disease Control and Prevention. Currently, no trea

5,6-DIHYDROPHENANTHRIDIN-5-YL AS AN ACTIVATABLE PROTECTING GROUP OF CARBOXYLIC ACID - A DIRECT PREPARATION OF AMIDES FROM 5-ACYL-5,6-DIHYDROPHENANTHRIDINE

Various amides are directly prepared from the protected carboxylic acids, 5-acyl-5,6-dihydrophenanthridines, by the reaction with primary amines in the presence of ceric pyridinium chloride and cupric oxide.