616241-13-5

Basic information

• Product Name: Benzenesulfonamide, N-[(1S)-1-(4-bromophenyl)-2-methylene-3-oxobutyl]-4-methyl-
• CAS NO: 616241-13-5
• Molecular Formula: C18H18BrNO3S
• Molecular Weight: 408.316
• Mol File: 616241-13-5.mol
• Article Data: 19

Chemical Properties

• CAS DataBase Reference: Benzenesulfonamide, N-[(1S)-1-(4-bromophenyl)-2-methylene-3-oxobutyl]-4-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonamide, N-[(1S)-1-(4-bromophenyl)-2-methylene-3-oxobutyl]-4-methyl-(616241-13-5)
• EPA Substance Registry System: Benzenesulfonamide, N-[(1S)-1-(4-bromophenyl)-2-methylene-3-oxobutyl]-4-methyl-(616241-13-5)

Safety Data

• Hazardous Substances Data: 616241-13-5(Hazardous Substances Data)

Upstream product

• 36176-90-6 N-(4-bromobenzylidene)-4-methylbenzenesulfonamide 
• 78-94-4 methyl vinyl ketone 
• 254428-47-2 (E)-N-(4-bromobenzylidene)-4-methylbenzenesulfonamide 

Relevant articles and documents

Asymmetric catalytic aza-Morita-Baylis-Hillman reaction using chiral bifunctional phosphine amides as catalysts

The asymmetric catalytic aza-Morita-Baylis-Hillman reaction of N-sulfonated imines with α,β-unsaturated ketones has been successfully conducted by using chiral bifunctional phosphine amides as catalysts. A series of new chiral bifunctional phosphine amide

Asymmetric aza-Morita-Baylis-Hillman reaction of N-sulfonated imines with activated olefins catalyzed by chiral phosphine Lewis bases bearing multiple phenol groups

In the aza-Morita-Baylis-Hillman reaction of N-sulfonated imines (N-arylmethylidene-4-methyl-benzenesulfonamides) with methyl vinyl ketone (MVK), ethyl vinyl ketone (EVK), and acrolein, we found that, through the use of catalytic amounts of chiral phosphi

Conformational lock in a Bronsted acid-Lewis base organocatalyst for the aza-Morita-Baylis-Hillman reaction

(S)-3-(N-Isopropyl-N-3-pyridinylaminomethyl)BINOL has been established as an efficient asymmetric bifunctional organocatalyst for the aza-MBH reaction. The acid-base functionalities cooperate in substrate activation and fixing of the organocatalyst confor

Chiral bifunctional organocatalysts bearing a 1,3-propanediamine unit for the aza-MBH reaction

The introduction of a 1,3-propanediamine unit at the 3-position of (S)-BINOL using a methylene spacer led to the formation of a chiral bifunctional organocatalyst for the aza-Morita-Baylis-Hillman (aza-MBH) reaction. The organocatalyst 1k mediated aza-MBH

Cooperativity in the counterion catalysis of Morita/Baylis/Hillman reactions promoted by enantioselective trifunctional organocatalysts

New trifunctional organocatalysts with a NHTs Br?nsted acid were prepared and tested in their ability to promote the counterion catalysis of generic and aza-Morita/Baylis/Hillman reactions.The cooperativity between the counterion and the NHTs Br?nsted aci