4910-26-3

Basic information

• Product Name: ethyl N-[(phenylsulfanyl)carbonyl]glycinate
• CAS NO: 4910-26-3
• Molecular Formula: C₁₁H₁₃NO₃S
• Molecular Weight: 239.2908
• Mol File: 4910-26-3.mol
• Article Data: 8

Chemical Properties

• Density: 1.23g/cm³
• Refractive Index: 1.567
• CAS DataBase Reference: ethyl N-[(phenylsulfanyl)carbonyl]glycinate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl N-[(phenylsulfanyl)carbonyl]glycinate(4910-26-3)
• EPA Substance Registry System: ethyl N-[(phenylsulfanyl)carbonyl]glycinate(4910-26-3)

Safety Data

• Hazardous Substances Data: 4910-26-3(Hazardous Substances Data)

Usage

General Description

Ethyl N-[(phenylsulfanyl)carbonyl]glycinate is a chemical compound that belongs to the class of glycine derivatives. It is a white crystalline solid at room temperature and is soluble in polar organic solvents. ethyl N-[(phenylsulfanyl)carbonyl]glycinate is widely used in organic synthesis as a building block for the preparation of various pharmaceuticals and agrochemicals. It has also been studied for its potential antimicrobial and anti-inflammatory properties. Ethyl N-[(phenylsulfanyl)carbonyl]glycinate has shown promise as a versatile intermediate in the development of new drugs and bioactive compounds.

Upstream product

• 2999-46-4 Ethyl isocyanoacetate 
• 80-17-1 benzenesufonyl hydrazide 
• 873-55-2 sodium benzenesulfonate 
• 108-98-5 thiophenol 
• 108-86-1 bromobenzene 
• 62076-10-2 (tert-butylsulfinyl)benzene 
• 13464-19-2 phenyl chlorothioformate 
• 459-73-4 GlyOEt*HCl 
• 98-09-9 benzenesulfonyl chloride 

Downstream Products

• 411212-95-8 N-phenylsulfanylcarbonyl-glycine-(N'-benzyloxycarbonyl-hydrazide) 
• 100616-49-7 N-(N-phenylsulfanylcarbonyl-glycyl)-alanine methyl ester 
• 109368-21-0 N-(N-benzyloxycarbonyl-glycyl)-N,N'-carbonyl-bis-glycine 
• 21639-45-2 N-phenylsulfanylcarbonyl-glycine 

Relevant articles and documents

Metal-Free Catalytic Synthesis of Thiocarbamates Using Sodium Sulfinates as the Sulfur Source

A novel molecular iodine-catalyzed protocol for the construction of thiocarbamates from readily available sodium sulfinates, isocyanides, and water has been described. The present methodology offers a facile and practical route to a variety of thiocarbamates in moderate to good yields with favorable functional group tolerance by use odorless sodium sulfinates as the sulfur source. The mechanistic studies suggest the present transformation involves a radical process.

Clean preparation of S-thiocarbamates with in situ generated hydroxide in 2-methyltetrahydrofuran

A simple and clean protocol for the synthesis of various alkyl and (hetero)aryl S-thiocarbamates was established. The usage of in situ generated hydroxide as both an oxygen source and hydrogen source as well as biomass-derived 2-methyltetrahydrofuran as a

Iodine-Catalyzed Odorless Synthesis of S-Thiocarbamates with Sulfonyl Chlorides as a Sulfur Source

A general and efficient protocol for the direct preparation of various S-thiocarbamates with readily available and inexpensive sulfonyl chlorides as an odorless sulfur source was developed. The employment of easily available reactants, excellent functiona