94771-83-2

Basic information

• Product Name: Benzenepropanoic acid, a-methylene-b-[[(4-methylphenyl)sulfonyl]amino]-, ethyl ester
• CAS NO: 94771-83-2
• Molecular Formula: C19H21NO4S
• Molecular Weight: 359.446
• Mol File: 94771-83-2.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzenepropanoic acid, a-methylene-b-[[(4-methylphenyl)sulfonyl]amino]-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenepropanoic acid, a-methylene-b-[[(4-methylphenyl)sulfonyl]amino]-, ethyl ester(94771-83-2)
• EPA Substance Registry System: Benzenepropanoic acid, a-methylene-b-[[(4-methylphenyl)sulfonyl]amino]-, ethyl ester(94771-83-2)

Safety Data

• Hazardous Substances Data: 94771-83-2(Hazardous Substances Data)

Upstream product

• 105479-98-9 ethyl 2-(acetoxy(phenyl)methyl)acrylate 
• 70-55-3 toluene-4-sulfonamide 
• 37442-45-8 ethyl 2-(hydroxy(phenyl)methyl)propenoate 
• 451491-99-9 C₂₀H₂₁NO₆S 
• 51608-60-7 N-(benzylidene)-p-methylbenzenesulfonamide 
• 140-88-5 ethyl acrylate 
• 51608-60-7 phenyl N-tosyl imine 
• 1170303-32-8 N-benzylidene-toluene-p-sulphonamide 

Downstream Products

• 84033-41-0 Ethyl-5-benzoyl-2-phenyl-1H-pyrrole-3-carboxylate 
• 212781-22-1 3t-phenyl-2-(4-chloro-benzyl)-acrylic acid ethyl ester 

Relevant articles and documents

1,3,5-triaza-7-phosphaadamantane (PTA): A practical and versatile nucleophilic phosphine organocatalyst

In this paper, the air-stable and readily available 1,3,5-triaza-7- phosphaadmantane (PTA) is reported as a practical and versatile nucleophilic phosphine organocatalyst. Under the mediation of 15-30 mol% of PTA, various electrophiles like aldehydes and i

Synthesis of unsaturated β-amino acid derivatives from carbamates of the Baylis-Hillman products

By treatment with a catalytic amount of DBU in DCM, N-p-toluenesulphonyl carbamates 6a-c, prepared starting from the corresponding Baylis-Hillman adducts, gave (E)-2-(p-toluenesulphonylaminomethyl)propenoates 3a-c, exclusively. On the contrary, changing D

Friedel-Crafts reaction of the Baylis-Hillman adducts of N-tosylimine derivatives

Friedel-Crafts reaction of aromatic compounds with the Baylis-Hillman adducts of N-tosylimine derivatives in the presence of sulfuric acid provided a stereoselective methodology for the preparation of 2-benzylsubstituted olefins in moderate yields.