13127-79-2

Basic information

• Product Name: N-benzenesulfonyl-bis(2-hydroxyethyl)amine
• Synonyms: N-benzenesulfonyl-bis(2-hydroxyethyl)amine
• CAS NO: 13127-79-2
• Molecular Weight: 245.299
• Mol File: 13127-79-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N-benzenesulfonyl-bis(2-hydroxyethyl)amine(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzenesulfonyl-bis(2-hydroxyethyl)amine(13127-79-2)
• EPA Substance Registry System: N-benzenesulfonyl-bis(2-hydroxyethyl)amine(13127-79-2)

Safety Data

• Hazardous Substances Data: 13127-79-2(Hazardous Substances Data)

Upstream product

• 75-21-8 oxirane 
• 98-10-2 benzenesulfonamide 
• 111-42-2 2,2'-iminobis[ethanol] 
• 98-09-9 benzenesulfonyl chloride 

Downstream Products

• 1623008-44-5 C₂₂H₂₁N₃O₈S 
• 102654-49-9 N,N-bis-(2-bromo-ethyl)-benzenesulfonamide 
• 58023-19-1 N-benzenesulfonyl-N,N-bis(2-chloroethyl)amine 
• 5033-21-6 4-benzenesulfonylmorpholine 

Relevant articles and documents

Synthesis and crystal structure of N,N-BIS[(4-aminophenoxy)ethyl]benzene sulfonamide

The reaction of diethanol amine and benzene sulfonyl chloride produced the benzene sulfonate intermediates, then it was nucleophilicly substituted by 4-nitrophenol and subsequently reduced by hydrazine hydrate in the presence of activated carbon and iron(

PROCESS FOR PREPARATION OF SUBSTANTIALLY OPTICALLY PURE LEVOROTATORY AND DEXTROROTATORY ENANTIOMERS OF CETIRIZINE USING NOVEL INTERMEDIATES

The present invention relates to a novel and commercially viable process for substantially optically pure levorotatory and dextrorotatory enantiomers of cetirizine intermediate, 1-[(4-chlorophenyl)phenylmethyl]piperazine, thereby producing substantially optically pure levorotatory and dextrorotatory enantiomers of cetirizine and their pharmaceutical acceptable acid addition salts thereof in high purity and in high yield using novel intermediates.