85828-29-1

Basic information

• Product Name: PHENYLSULFONYL-L-SERINE
• Synonyms: PHENYLSULFONYL-L-SERINE;N-(Phenylsulfonyl)-L-serine
• CAS NO: 85828-29-1
• Molecular Formula: C₉H₁₁NO₅S
• Molecular Weight: 245.25
• Mol File: 85828-29-1.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: PHENYLSULFONYL-L-SERINE(CAS DataBase Reference)
• NIST Chemistry Reference: PHENYLSULFONYL-L-SERINE(85828-29-1)
• EPA Substance Registry System: PHENYLSULFONYL-L-SERINE(85828-29-1)

Safety Data

• Hazardous Substances Data: 85828-29-1(Hazardous Substances Data)

Upstream product

• 56-45-1 L-serin 
• 98-09-9 benzenesulfonyl chloride 

Downstream Products

• 88425-31-4 (S)-2-(N-(phenylsulfonyl)amino)-1-hydroxy-3-hexanone 
• 119593-24-7 (S)-3-<(phenylsulfonyl)amino>-4-hydroxy-1-(methylthio)-2-butanone 
• 144422-81-1 N-phenylsulphonyl-4-exomethylene-(S)-proline benzylester 
• 144422-80-0 N-phenylsulphonyl-N-propargyl-3-bromo-(S)-alanine benzylester 
• 144422-79-7 N-phenylsulphonyl-O-tetrahydropyranyl-(S)-serine benzylester 
• 144423-03-0 N-phenylsulphonyl-N-propargyl-O-tetrahydropyranyl-(S)-serine benzylester 
• 119593-77-0 (2R,3R)-N-(phenylsulfonyl)-3-hydroxyproline 
• 119593-55-4 (2R,3S)-3-<(phenylsulfonyl)amino>-2,4-dihydroxy-1-(methylthio)butane 
• 119593-56-5 (2S,3S)-3-<(phenylsulfonyl)amino>-2,4-dihydroxy-1-(methylthio)butane 
• 119593-25-8 (4S,5S)-5-<(phenylsulfonyl)amino>-4,6-dihydroxyhexene 
• 119593-26-9 (4R,5S)-5-<(phenylsulfonyl)amino>-4,6-dihydroxyhexene 
• 119593-52-1 (2S,3S)-3-hydroxy-2-(hydroxymethyl)-1-(phenylsulfonyl)pyrrolidine 
• 119593-53-2 (2S,3R)-3-hydroxy-2-(hydroxymethyl)-1-(phenylsulfonyl)pyrrolidine 
• 119593-50-9 (2S)-2-[(phenylsulfonyl)amino]-5-chloro-1-hydroxy-3-pentanone 

Relevant articles and documents

Design, synthesis, molecular docking, antimicrobial, and antioxidant activities of new phenylsulfamoyl carboxylic acids of pharmacological interest

The research explores the facile synthesis of some new phenylsulfamoyl carboxylic acids, their molecular docking, antimicrobial, and antioxidant activities. The procedure involved the mild reaction of amino acids with benzenesulfonyl chloride in a medium

IMIDAZOLIDINONE DERIVATIVES

The invention is concerned with novel imidazolidinone derivatives of formula (I): wherein R1 to R11 and X are as defined in the description and in the claims, as well as physiologically acceptable salts thereof. These compounds bind

N-Acylated α-Amino Acids as Novel Oral Delivery Agents for Proteins

A series of N-acylated α-amino acids were synthesized and shown to improve the oral delivery of two protein drugs, salmon calcitonin (sCT) and interferon-α.Forty-five compounds in this series were tested in vivo in rats and primates.A significant positive