3445-53-2

Basic information

• Product Name: 3-(Phenylsulfonyl)propanoyl chloride
• Synonyms: 3-(Phenylsulfonyl)propanoyl chloride;3-(Phenylsulphonyl)propanoyl chloride
• CAS NO: 3445-53-2
• Molecular Formula: C₉H₉ClO₃S
• Molecular Weight: 232.68396
• Mol File: 3445-53-2.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-(Phenylsulfonyl)propanoyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(Phenylsulfonyl)propanoyl chloride(3445-53-2)
• EPA Substance Registry System: 3-(Phenylsulfonyl)propanoyl chloride(3445-53-2)

Safety Data

• Hazardous Substances Data: 3445-53-2(Hazardous Substances Data)

Upstream product

• 49639-31-8 3-benzenesulfinyl-propionic acid 
• 10154-71-9 3-(phenylsulfonyl)propionic acid 

Downstream Products

• 119888-93-6 3-Benzenesulfonyl-propionic acid 1-methyl-allyl ester 
• 119888-94-7 3-Benzenesulfonyl-propionic acid 1-phenyl-allyl ester 
• 119888-95-8 3-Benzenesulfonyl-propionic acid 1-benzyloxymethyl-allyl ester 
• 10154-71-9 3-(phenylsulfonyl)propionic acid 
• 340011-42-9 N-(4-methylphenyl)-3-(phenylsulfonyl)propanamide 
• 340011-45-2 N-(4-chlorophenyl)-3-(phenylsulfonyl)propanamide 
• 340011-43-0 N-(4-methoxyphenyl)-3-(phenylsulfonyl)propanamide 
• 93472-54-9 N-phenyl-3-(phenylsulfonyl)propanamide 
• 340011-44-1 N-(4-fluorophenyl)-3-(phenylsulfonyl)propanamide 
• 340011-46-3 N-(4-bromophenyl)-3-(phenylsulfonyl)propanamide 
• 314021-31-3 3-benzenesulfonyl-N-methoxy-N-methyl-propionamide 
• 314021-42-6 (4Z,8E)-(S)-1-Benzenesulfonyl-12-(tert-butyl-diphenyl-silanyloxy)-7-triethylsilanyloxy-dodeca-4,8-dien-3-one 
• 314021-30-2 (E)-(S)-1-Benzenesulfonyl-12-(tert-butyl-diphenyl-silanyloxy)-7-triethylsilanyloxy-dodec-8-en-4-yn-3-one 
• 314021-43-7 {5-[6-(2-benzenesulfonyl-ethyl)-6-methoxy-3,6-dihydro-2H-pyran-2-yl]-pent-4-enyloxy}-tert-butyl-diphenyl-silane 

Relevant articles and documents

Second generation of fucose-based DC-SIGN ligands: Affinity improvement and specificity versus Langerin

DC-SIGN and Langerin are two C-type lectins involved in the initial steps of HIV infections: the former acts as a viral attachment factor and facilitates viral invasion of the immune system, the latter has a protective effect. Potential antiviral compounds targeted against DC-SIGN were synthesized using a common fucosylamide anchor. Their DC-SIGN affinity was tested by SPR and found to be similar to that of the natural ligand Lewis-X (LeX). The compounds were also found to be selective for DC-SIGN and to interact only weakly with Langerin. These molecules are potentially useful therapeutic tools against sexually transmitted HIV infection.