77198-99-3

Basic information

• Product Name: N-PHENETHYLBENZENESULFONAMIDE
• Synonyms: N-PHENETHYLBENZENESULFONAMIDE;N-(2-phenylethyl)benzenesulfonamide
• CAS NO: 77198-99-3
• Molecular Formula: C₁₄H₁₅NO₂S
• Molecular Weight: 261.3394
• Mol File: 77198-99-3.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 422.6°C at 760 mmHg
• Flash Point: 209.4°C
• Appearance: /
• Density: 1.203g/cm³
• Vapor Pressure: 2.39E-07mmHg at 25°C
• Refractive Index: 1.588
• CAS DataBase Reference: N-PHENETHYLBENZENESULFONAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-PHENETHYLBENZENESULFONAMIDE(77198-99-3)
• EPA Substance Registry System: N-PHENETHYLBENZENESULFONAMIDE(77198-99-3)

Safety Data

• Hazardous Substances Data: 77198-99-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C14H15NO2S/c16-18(17,14-9-5-2-6-10-14)15-12-11-13-7-3-1-4-8-13/h1-10,15H,11-12H2

Upstream product

• 64-04-0 phenethylamine 
• 98-09-9 benzenesulfonyl chloride 
• 92200-24-3 2-phenyl-N-(phenylsulfonyl)acetamide 
• 98-11-3 benzenesulfonic acid 
• 140-29-4 phenylacetonitrile 
• 670-98-4 methyl benzenesulfinate 
• 98-10-2 benzenesulfonamide 
• 60-12-8 2-phenylethanol 
• 29281-83-2 4-methylbenzensulphonamide potassium salt 
• 873-55-2 sodium benzenesulfonate 

Downstream Products

• 175287-91-9 2-benzenesulfonyl-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid ethyl ester 
• 81114-41-2 1-benzenesulfonyl-2,3-dihydro-1H-indole 
• 72131-28-3 N-(4-hydroxyphenethyl)benzenesulfonamide 
• 618-41-7 Benzenesulfinic acid 
• 1415586-20-7 C₁₇H₂₀N₂O₄S 
• 1071493-68-9 C₁₄H₁₄INO₂S 
• 73355-73-4 N-methyl-N-phenethyl-N'-phenyl-urea 
• 73355-76-7 N-methyl-N'-[1]naphthyl-N-phenethyl-urea 
• 88612-00-4 3,4-dihydro-isoquinoline-1-carboxylic acid ethyl ester 
• 50458-78-1 ethyl isoquinoline-1-carboxylate 

Relevant articles and documents

A kinetic analysis of the effects of β-phenylethylamine on the concentrations of dopamine and its metabolites in the rat striatum

The purpose of this investigation was to determine whether the increase in the dopamine (DA) concentration in the rat striatum after a rapid iv injection of β-phenylethylamine (PEA) can be quantitatively explained by the alteration of the striatum PEA con

A Novel Method for Preparation of 2-Chloro Enesulfonamides

A novel method for the synthesis of 2-chloro enesulfonamides via the one-pot addition-elimination of N-chloro-N-fluorobenzenesulfonamides (CFBSA) to styrenes in the presence of Et3N is described. A total of 20 examples are presented to illustrate this concept including various of styrenes.

Highly efficient one-pot synthesis of N-alkyl sulfonamides from alcohols using N-(p-toluenesulfonyl) imidazole (Tsim)

A facile and efficient method for one-pot synthesis of N-alkyl sulfonamides from alcohols using N-(p-toluenesulfonyl)imidazole (TsIm) is described. In this protocol, treatment of various potassium sulfonylamide salts and alcohols in the presence of TsIm and triethylamine in refluxing DMF furnishes the corresponding N-alkyl sulfonamides in good to excellent yields. This methodology is highly efficient for reaction of various structurally diverse primary and secondary alcohols as well as potassium sulfonylamides. Also, the density functional theoretical calculations are employed to mechanistically study this protocol. [Supplementary materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements for the following free supplemental files: Additional text and figures.]