76616-47-2

Basic information

• Product Name: N-[(4-methylphenyl)sulfonyl]-β-alanine ethyl ester
• Synonyms: N-[(4-methylphenyl)sulfonyl]-β-alanine ethyl ester
• CAS NO: 76616-47-2
• Molecular Weight: 271.337
• Mol File: 76616-47-2.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: N-[(4-methylphenyl)sulfonyl]-β-alanine ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: N-[(4-methylphenyl)sulfonyl]-β-alanine ethyl ester(76616-47-2)
• EPA Substance Registry System: N-[(4-methylphenyl)sulfonyl]-β-alanine ethyl ester(76616-47-2)

Safety Data

• Hazardous Substances Data: 76616-47-2(Hazardous Substances Data)

Upstream product

• 64-17-5 ethanol 
• 4816-80-2 N-tosyl-L-glutamic acid 
• 140-88-5 ethyl acrylate 
• 55962-05-5 [N-(p-tolylsulfonyl)imino]phenyliodinane 
• 70-55-3 toluene-4-sulfonamide 
• 172265-24-6 ethyl-N-tosyl-aziridine-2-carboxylate 
• 42908-33-8 3-{[(4-methylphenyl)sulfonyl]amino}propanoic acid 
• 96229-31-1 ethyl 3-(p-toluenesulfonylamino)-propionimidate hydrochloride 

Downstream Products

• 76616-44-9 7-bromo-5-(p-tolylsulphonyl)-4,5,6,7-tetrahydro-8H-thieno<3,2-c>azepin-8-one 
• 76616-49-4 N-(3-thenyl)-N-(p-tolylsulphonyl)-β-alanine 
• 76616-42-7 5-(p-tolylsulphonyl)-4,5,6,7-tetrahydro-8H-thieno<3,2-c>azepin-8-one 
• 76616-48-3 ethyl N-(3-thenyl)-N-(p-tolylsulphonyl)-β-alanate 
• 88831-41-8 N-(β-Benzoylethyl)-N-tosyl-3-aminopropionsaeureethylester 

Relevant articles and documents

Highly efficient KF/Al2O3-catalyzed versatile hetero-Michael addition of nitrogen, oxygen, and sulfur nucleophiles to α,β-ethylenic compounds

The first example of KF/Al2O3-catalyzed versatile hetero-Michael addition reaction of nitrogen, oxygen, and sulfur nucleophiles was developed for facile preparation of organic compounds of widely different structures. In contrast with the existing methods using many acidic catalysts, this method is very general, simple, high-yielding, environmentally friendly, and oxygen and moisture tolerant.

The zeolite ZSM-5-SO3H catalyzed aza-Michael addition of amines and sulfonamides to electron-deficient alkenes under solventfree conditions

Aza-Micheal addition of aromatic and aliphatic amines and sulfonamides to α,β-unsaturated esters, ketones and nitriles has been developed using the zeolite ZSM-5-SO3H as catalyst under solvent-free conditions.

Reduction of 2-acylaziridines by samarium(II) iodide. An efficient and regioselective route to β-amino carbonyl compounds

A convenient method for the reduction of 2-acylaziridines, aziridine-2- carboxylates and aziridine-2-carboxamides is described. The reduction of all of the substrates examined was extremely rapid and highly regioselective, giving rise to β-amino carbonyl compounds. This method appears to be general for all of the classes of aziridines mentioned above, and also tolerates a variety of nitrogen protecting groups.