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N-(2-formyl-3-methylphenyl)-4-methylbenzenesulfonamide

Base Information Edit
  • Chemical Name:N-(2-formyl-3-methylphenyl)-4-methylbenzenesulfonamide
  • CAS No.:1242061-78-4
  • Molecular Formula:C15H15NO3S
  • Molecular Weight:289.355
  • Hs Code.:
  • Mol file:1242061-78-4.mol
N-(2-formyl-3-methylphenyl)-4-methylbenzenesulfonamide

Synonyms:N-(2-formyl-3-methylphenyl)-4-methylbenzenesulfonamide

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Chemical Property of N-(2-formyl-3-methylphenyl)-4-methylbenzenesulfonamide Edit
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Technology Process of N-(2-formyl-3-methylphenyl)-4-methylbenzenesulfonamide

There total 11 articles about N-(2-formyl-3-methylphenyl)-4-methylbenzenesulfonamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With silver hexafluoroantimonate; [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; 2-amino-4-trifluoromethylbenzoic acid; In ethanol; at 80 ℃; for 12h; Reagent/catalyst; Solvent; Sealed tube;
DOI:10.1055/s-0036-1591765
Guidance literature:
4-toluenesulfonyl azide; N-(4-methoxyphenyl)-1-(o-tolyl)methanimine; With bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]; silver(I) hexafluorophosphate; In 1,2-dichloro-ethane; at 100 ℃; for 12h; Sealed tube; Schlenk technique;
With hydrogenchloride; In tetrahydrofuran; water; at 20 ℃;
DOI:10.1002/chem.201603805
Guidance literature:
4-toluenesulfonyl azide; N-(2-methylphenyl)methylidene-4-methylbenzenesulfonamide; With bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]; silver(I) triflimide; In 1,2-dichloro-ethane; at 60 ℃; for 12h; Schlenk technique;
With hydrogenchloride; In water; at 20 ℃; for 3h; Solvent; Reagent/catalyst; Temperature; Catalytic behavior; Schlenk technique;
DOI:10.1021/acs.orglett.6b02406
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