4-methoxy-N-(4-methylbenzylidene)benzenesulfonamide

Base Information

Chemical Name:4-methoxy-N-(4-methylbenzylidene)benzenesulfonamide
CAS No.:1056904-01-8
Molecular Formula:C₁₅H₁₅NO₃S
Molecular Weight:289.355
Hs Code.:

Synonyms:4-methoxy-N-(4-methylbenzylidene)benzenesulfonamide

Suppliers and Price of 4-methoxy-N-(4-methylbenzylidene)benzenesulfonamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 4-methoxy-N-(4-methylbenzylidene)benzenesulfonamide

Chemical Property:

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Technology Process of 4-methoxy-N-(4-methylbenzylidene)benzenesulfonamide

There total 1 articles about 4-methoxy-N-(4-methylbenzylidene)benzenesulfonamide 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:

Reference yield:

: 106-42-3
para-xylene

: 1129-26-6
4-methoxybenzene sulfonamide

: 1056904-01-8
4-methoxy-N-(4-methylbenzylidene)benzenesulfonamide

Guidance literature:: With oxygen; at 120 ℃; for 24h; under 7500.75 Torr; Autoclave;
DOI:10.1039/c2cc31438j

Reference yield: 99.0%

: 1629-58-9
4-penten-3-one

: 1056904-01-8
4-methoxy-N-(4-methylbenzylidene)benzenesulfonamide

: 1191128-11-6
C₂₀H₂₃NO₄S

Guidance literature:: With C₃₄H₃₁N₃O₂; β-naphthol; In dichloromethane; at -50 ℃; for 48h; optical yield given as %ee; enantioselective reaction; Inert atmosphere;
DOI:10.1021/ol901920s

Reference yield: 99.0%

: 1056904-01-8
4-methoxy-N-(4-methylbenzylidene)benzenesulfonamide

: 78-94-4,25038-87-3
methyl vinyl ketone

: 1191128-02-5
C₁₉H₂₁NO₄S

Guidance literature:: With C₃₄H₃₁N₃O₂; β-naphthol; In dichloromethane; at -50 ℃; for 48h; optical yield given as %ee; enantioselective reaction; Inert atmosphere;
DOI:10.1021/ol901920s