340696-10-8

Basic information

• Product Name: Benzenesulfonamide, N-[2-(hydroxyphenylmethyl)phenyl]-4-methyl-
• CAS NO: 340696-10-8
• Molecular Formula: C20H19NO3S
• Molecular Weight: 353.442
• Mol File: 340696-10-8.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzenesulfonamide, N-[2-(hydroxyphenylmethyl)phenyl]-4-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonamide, N-[2-(hydroxyphenylmethyl)phenyl]-4-methyl-(340696-10-8)
• EPA Substance Registry System: Benzenesulfonamide, N-[2-(hydroxyphenylmethyl)phenyl]-4-methyl-(340696-10-8)

Safety Data

• Hazardous Substances Data: 340696-10-8(Hazardous Substances Data)

Upstream product

• 6590-65-4 N-(2-Formyl-phenyl)-4-methyl-benzenesulfonamide 
• 100-58-3 phenylmagnesium bromide 
• 5176-12-5 (2-nitrophenyl)phenylmethanol 
• 13209-38-6 (2-aminophenyl)(phenyl)methanol 
• 98-59-9 p-toluenesulfonyl chloride 
• 90312-02-0 N-(2-hydroxymethylphenyl)-4-methylbenzenesulfonamide 
• 5344-90-1 2-Aminobenzyl alcohol 
• 591-51-5 phenyllithium 
• 2835-77-0 (2-aminophenyl)(phenyl)methanone 
• 1859-71-8 2-(tosylamino)benzophenone 

Downstream Products

• 340696-22-2 4-methyl-N-{2-[(5-methylfuran-2-yl)(phenyl)methyl]phenyl}-benzenesulfonamide 

Relevant articles and documents

Copper-Catalyzed (4+1) Cascade Annulation of Terminal Alkynes with 2-(Tosylmethyl)anilines: Synthesis of 2,3-Disubstituted Indoles

A novel strategy based on Cu-catalyzed (4+1) cascade annulation of terminal alkynes as one-carbon synthons with 2-(tosylmethyl)anilines has been developed for the expeditious synthesis of 2,3-disubstituted indoles, in which in situ generations of aza-o-quinone methides and alkynyl-copper(I) species are involved. This annulation provides an effective method for the assembly of synthetically and structurally interesting 2,3-disubstituted indoles.

Diastereoselective synthesis of 2,4-substituted tetrahydroquinolines via hf(otf)4-catalyzed substitution/cyclization of 2-aminobenzyl alcohols with styrenes

An efficient and convenient stereoselective synthetic approach to 2,4-substituted 1,2,3,4-tetrahydroquinoline has been developed. This catalytic procedure involves a sequential reaction of 2-aminobenzyl alcohol with styrenes in the presence of Hf(OTf)4 ca

Broensted acid-catalyzed one-pot synthesis of indoles from o-aminobenzyl alcohols and furans

Broensted acid-catalyzed one-pot synthesis of indoles from o-aminobenzyl alcohols and furans has been developed. This method operates via the in situ formation of aminobenzylfuran, followed by its recyclization into the indole core. The method proved to be efficient for substrates possessing different functional groups, including -OMe, -CO2Cy, and -Br. The resulting indoles can easily be transformed into diverse scaffolds, including 2,3- and 1,2-fused indoles, and indoles possessing an α,β-unsaturated ketone moiety at the C-2 position.