30057-92-2

Basic information

• Product Name: N-(2-OXO-2-PHENYLETHYL)-P-TOLUENE-SULFONAMIDE)
• Synonyms: N-(2-OXO-2-PHENYLETHYL)-P-TOLUENE-SULFONAMIDE);1-Phenyl-2-(tosylamino)ethanone;4-Methyl-N-(2-oxo-2-phenylethyl)benzenesulfonamide;N-(β-Oxophenethyl)-p-toluenesulfonamide;N-Phenacyl-p-toluenesulfonamide;Phenyl(tosylaminomethyl) ketone;α-(Tosylamino)acetophenone;N-(2-keto-2-phenyl-ethyl)-4-methyl-benzenesulfonamide
• CAS NO: 30057-92-2
• Molecular Formula: C₁₅H₁₅NO₃S
• Molecular Weight: 289.36
• Mol File: 30057-92-2.mol
• Article Data: 43

Chemical Properties

• Boiling Point: 466.7°C at 760 mmHg
• Flash Point: 236.1°C
• Appearance: /
• Density: 1.245g/cm³
• Vapor Pressure: 6.91E-09mmHg at 25°C
• Refractive Index: 1.585
• CAS DataBase Reference: N-(2-OXO-2-PHENYLETHYL)-P-TOLUENE-SULFONAMIDE)(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-OXO-2-PHENYLETHYL)-P-TOLUENE-SULFONAMIDE)(30057-92-2)
• EPA Substance Registry System: N-(2-OXO-2-PHENYLETHYL)-P-TOLUENE-SULFONAMIDE)(30057-92-2)

Safety Data

• Hazardous Substances Data: 30057-92-2(Hazardous Substances Data)

Usage

InChI:InChI=1/C15H15NO3S/c1-12-7-9-14(10-8-12)20(18,19)16-11-15(17)13-5-3-2-4-6-13/h2-10,16H,11H2,1H3

Upstream product

• 52109-50-9 2-(Methylthio)-2-(p-toluolsulfonamido)acetophenon 
• 13735-81-4 1-styrenyloxytrimethylsilane 
• 55962-05-5 [N-(p-tolylsulfonyl)imino]phenyliodinane 
• 135733-17-4 O-Benzyl-N-phenacyl-N-tosylhydroxylamine 
• 135733-19-6 α-(4-Bromobenzyloxy)-N-tosylphenacylamine 
• 79866-24-3 N-acetyl-N-tosylphenacylamine 
• 135733-20-9 O-(Tetrahydro-2H-pyran-2-yl)-N-tosylhydroxylamine 
• 70-11-1 α-bromoacetophenone 
• 5468-37-1 2-aminoacetophenone hydrochloride 
• 98-59-9 p-toluenesulfonyl chloride 
• 24395-14-0 N-(p-tolylsulfonyl)-2-phenylaziridine 
• 37394-53-9 ω-aminoacetophenone hydrobromide 
• 17639-66-6 1-tosyl-1H-pyrrole-2-carboxylic acid 
• 100-42-5 styrene 

Downstream Products

• 100970-17-0 N-nitroso-N-phenacyl-toluene-4-sulfonamide 
• 56157-01-8 N,4-dimethyl-N-(2-oxo-2-phenylethyl)benzenesulfonamide 
• 30057-97-7 N-Tosyl-N-benzyl-α-aminoacetophenon 
• 149286-01-1 2-(N-tosylamino)-1-phenyl-1-ethanol 
• 149286-01-1 (R)-N-(2-hydroxy-2-phenylethyl)-4-methylbenzenesulfonamide 
• 79866-24-3 N-acetyl-N-tosylphenacylamine 
• 2549-14-6 (R)-2-Amino-1-phenylethanol 
• 104-15-4 toluene-4-sulfonic acid 
• 100970-15-8 2-phenyl-N-(toluene-4-sulfonyl)-glyoxylamide oxime 
• 1017294-96-0 C₂₅H₂₀N₄O₅S 
• 1017294-94-8 C₂₅H₂₁N₃O₃S 
• 1017294-95-9 C₂₆H₂₃N₃O₄S 
• 1220572-68-8 2-amino-5-benzoyl-N-butyl-4-(pyridin-2-yl)-1H-pyrrole-3-carboxamide 
• 1220572-67-7 2-amino-5-benzoyl-N-cyclopropyl-4-(pyridin-4-yl)-1H-pyrrole-3-carboxamide 

Relevant articles and documents

A mild and efficient synthesis of α-tosylamino ketones from aryl aziridines in the presence of β-cyclodextrin and NBS in water

NBS has been utilized for the first time for the oxidative cleavage of aryl aziridines involving β-cyclodextrin-aziridine complexes in water to give the corresponding α-amino ketones in high yields.

Expanding the Protecting Group Scope for the Carbonyl Olefin Metathesis Approach to 2,5-Dihydropyrroles

Chiral pyrrolidine derivatives are important building blocks for natural product synthesis. Carbonyl olefin metathesis has recently emerged as a powerful tool for the construction of such building blocks from chiral amino acid derivatives. Here, we demons

The reaction of prop-2-ynylsulfonium salts and sulfonyl-protected β-amino ketones to epoxide-fused 2-methylenepyrrolidines and S-containing pyrroles

A novel divergent domino annulation reaction of prop-2-ynylsulfonium salts with sulfonyl-protected β-amino ketones has been developed, affording various epoxide-fused 2-methylenepyrrolidines and S-containing pyrroles in moderate to excellent yields. Prop-2-ynylsulfonium salts act as C2synthons in the reactions providing a promising epoxide-fused skeleton in a single operation with readily accessible starting materials.