7473-89-4

Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
Ethyl N-(cyclohexylcarbonyl)glycinate is used as a building block for the synthesis of various pharmaceuticals and agrochemicals. Its versatile chemical structure allows for the creation of a wide range of biologically active compounds.
Used in Organic Chemistry:
Ethyl N-(cyclohexylcarbonyl)glycinate is used as a reagent for the synthesis of various alcohol and amine derivatives. Its unique properties make it a valuable component in the development of new organic compounds.
Used in Pesticide and Herbicide Production:
Ethyl N-(cyclohexylcarbonyl)glycinate is used in the production of pesticides, herbicides, and other biologically active compounds. Its ability to form stable derivatives makes it a useful component in the development of effective agricultural chemicals.
Used in Food and Beverage Industry:
Ethyl N-(cyclohexylcarbonyl)glycinate is used as an additive in the food and beverage industry. Its properties may contribute to the enhancement of flavor, texture, or other qualities in various food products.

Upstream product

• 64-17-5 ethanol 
• 32377-88-1 (cyclohexanecarbonyl-amino)-acetic acid 
• 1499-53-2 ethyl hippurate 
• 623-33-6 glycine ethyl ester hydrochloride 
• 2719-27-9 cyclohexanylcarbonyl chloride 
• 64-19-7 acetic acid 
• 2043-61-0 cyclohexanecarbaldehyde 
• 98-88-4 benzoyl chloride 
• 2949-22-6 Glycine ethyl ester isocyanate 

Downstream Products

• 100052-07-1 (5-cyclohexyl-tetrazol-1-yl)-acetic acid ethyl ester 
• 32377-88-1 (cyclohexanecarbonyl-amino)-acetic acid 
• 161198-52-3 {[1-Cyclohexyl-1-methylsulfanyl-meth-(E)-ylidene]-amino}-acetic acid ethyl ester 
• 42470-01-9 2-cyclohexyl-oxazole-4,5-dicarboxylic acid diethyl ester 

Relevant academic research and scientific papers

1-(Piperidin-4-yl)-2-benzimidazolone compounds and application thereof

The invention belongs to the technical field of medicines, and relates to novel 1-(piperidin-4-yl)-2-benzimidazolone compounds, a composition containing the compounds, and a use of the compounds or the composition as human immunodeficiency virus (HIV ) integrase inhibitor. The compounds are used for the antiviral treatment of 2-or-more-years-old HIV-infected persons. The above drugs act on HIV integrase to prevent HIV replication in order to reduce the HIV viral load in blood. The structure of the compounds is represented by general formula (I), and R1 and R2 in the general formula (I) are asdefined in the claims and the description.

Nickel/Photoredox-Catalyzed Amidation via Alkylsilicates and Isocyanates

A nickel/photoredox, dual-catalyzed amidation reaction between alkylsilicate reagents and alkyl/aryl isocyanates is reported. In contrast to the previously reported reductive coupling process, this protocol is characterized by mild reaction conditions and the absence of a stoichiometric reductant. A mechanistic hypothesis involving a nickel-isocyanate adduct is proposed based on literature precedent and further validation by experimental results.

Highly efficient oxidative amidation of aldehydes with amine hydrochloride salts

A mild and efficient copper-catalyzed oxidative amidation of aldehydes was developed using amine HCl salts and tert-butyl hydroperoxide as an oxidant. Copyright

Synthesis of oxazoles and thiazoles using thioimidates

Several oxazoles and thiazoles were synthesized easily by the reaction of N-(methylthioalkylidene)glycine ethyl ester with diethyl oxalate, acid halides, and thionesters in the presence of base.