177972-59-7

Basic information

• Product Name: N-[(3Z)-hex-3-en-1-yl](4-methylphenyl)sulfonamide
• Synonyms: N-[(3Z)-hex-3-en-1-yl](4-methylphenyl)sulfonamide
• CAS NO: 177972-59-7
• Molecular Weight: 253.365
• Mol File: 177972-59-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N-[(3Z)-hex-3-en-1-yl](4-methylphenyl)sulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[(3Z)-hex-3-en-1-yl](4-methylphenyl)sulfonamide(177972-59-7)
• EPA Substance Registry System: N-[(3Z)-hex-3-en-1-yl](4-methylphenyl)sulfonamide(177972-59-7)

Safety Data

• Hazardous Substances Data: 177972-59-7(Hazardous Substances Data)

Upstream product

• 1002-28-4 3-hexyn-1-ol 
• 18303-04-3 N-[(tert-butoxy)carbonyl]-4-methylbenzenesulfonamide 
• 928-96-1 (Z)-3-Hexen-1-ol 
• 126745-58-2 1,1-dimethylethyl (Z)-3-hexenyl[(4-methylphenyl)sulfonyl]carbamate 

Downstream Products

• 124920-12-3 2-ethyl-1-(toluene-4-sulfonyl)-pyrrolidine 
• 406179-88-2 1-(p-toluenesulfonyl)-5-vinyl-2,3-dihydro-1H-pyrrole 

Relevant articles and documents

Synthesis of cyclic dienamide using ruthenium-catalyzed ring-closing metathesis of ene-ynamide

Ring-closing metathesis of ene-ynamide, which has alkene and ynamide moieties in a molecule, using a second-generation ruthenium carbene complex produced nitrogen-containing heterocycles, which have a dienamide moiety, in high yields. Diels-Alder reaction

A stereochemically flexible approach to pyrrolidines based on 5-endo-trig iodocyclisations of homoallylic sulfonamides

5-endo-trig Iodocyclisations of the (E)-homoallylic sulfonamides 24 in the presence of potassium carbonate give excellent yields of trans-2,5-disubstituted-3-iodopyrrolidines 36. In the absence of base, these initial kinetic products undergo rapid isomeri