69398-48-7

Basic information

• Product Name: N-(Phenylsulfonyl)glycine Methyl Ester
• Synonyms: N-(Phenylsulfonyl)glycine Methyl Ester;Methyl 2-(phenylsulfonamido)acetate
• CAS NO: 69398-48-7
• Molecular Formula: C₉H₁₁NO₄S
• Molecular Weight: 229.25294
• Mol File: 69398-48-7.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: N-(Phenylsulfonyl)glycine Methyl Ester(CAS DataBase Reference)
• NIST Chemistry Reference: N-(Phenylsulfonyl)glycine Methyl Ester(69398-48-7)
• EPA Substance Registry System: N-(Phenylsulfonyl)glycine Methyl Ester(69398-48-7)

Safety Data

• Hazardous Substances Data: 69398-48-7(Hazardous Substances Data)

Usage

General Description

N-(Phenylsulfonyl)glycine Methyl Ester is a chemical compound that belongs to the class of sulfonyl compounds. It is a glycine derivative with a phenylsulfonyl group attached to the nitrogen atom. N-(Phenylsulfonyl)glycine Methyl Ester is often used as a reagent for the synthesis of various organic compounds and pharmaceuticals. It has been found to exhibit potential biological activity, making it a useful building block in drug discovery and development. Additionally, it has been utilized in synthetic chemistry as a versatile reagent for the preparation of diverse compounds due to its stability and reactivity.

Upstream product

• 67-56-1 methanol 
• 5398-96-9 N-phenylsulfonylglycine 
• 50487-70-2 N-allylbenzenesulfonamide 
• 5680-79-5 glycine ethyl ester hydrochloride 
• 98-09-9 benzenesulfonyl chloride 

Downstream Products

• 265669-17-8 N-Phenylsulfonyl-α-bromoglycine methyl ester 
• 195379-95-4 (Allyl-benzenesulfonyl-amino)-acetic acid methyl ester 
• 195379-98-7 [Benzenesulfonyl-(3-methyl-but-2-enyl)-amino]-acetic acid methyl ester 
• 331731-75-0 (benzenesulfonyl-prop-2-ynyl-amino)-acetic acid methyl ester 
• 60160-52-3 phenylsulfonylaminoacetic acid hydrazide 
• 40788-59-8 2-methylbenzimidazole 
• 543725-66-2 N-[2-(3-methyl-5-oxo-4,5-dihydro-pyrazol-1-yl)-2-oxo-ethyl]-benzenesulfonamide 
• 317336-65-5 N-[1-(4-Chloro-phenyl)-meth-(E)-ylidene-hydrazinocarbonylmethyl]-benzenesulfonamide 
• 59724-68-4 N-benzenesulfonyl-alanine methyl ester 
• 1071118-70-1 [(E)-Benzenesulfonylimino]-acetic acid methyl ester 
• 195380-04-2 N-allyl-N-(2-oxoethyl)benzenesulfonamide 
• 195380-06-4 N-(3-Methyl-but-2-enyl)-N-(2-oxo-ethyl)-benzenesulfonamide 

Relevant articles and documents

Synthesis, characterization and antifungal activities of some benzenesulphonylamino acid derivatives

Condensation of benzenesulphonyl chloride (1) with a series of amino acids afforded benzenesulphonylamino acids (2a-d). Esterification of the derivatives (2a-d) in methanol gave the corresponding benzensulphonylamino acid methylesters (3a-d), which conden

Palladium-catalysed asymmetric allylic substitution: Synthesis of α- and β-amino acids

Methodology has been established for the formation of enantiomerically enriched α-amino acids using palladium-catalysed allylic amination. The formation of enantiomerically enriched allylamines has been achieved with high enantioselectivity. Oxidative cleavage of the allylamines provides arylglycine and glutamic acid derivatives. Additionally, enantiomerically enriched β-amino acids have been prepared in high enantiomeric excess. Palladium-catalysed asymmetric allylic substitution is used as the key synthetic transformation.