N-[1-Morpholin-4-yl-1-phenyl-meth-(Z)-ylidene]-C-phenyl-methanesulfonamide

Base Information

Chemical Name:N-[1-Morpholin-4-yl-1-phenyl-meth-(Z)-ylidene]-C-phenyl-methanesulfonamide
CAS No.:134772-64-8
Molecular Formula:C₁₈H₂₀N₂O₃S
Molecular Weight:344.434
Hs Code.:

Synonyms:N-[1-Morpholin-4-yl-1-phenyl-meth-(Z)-ylidene]-C-phenyl-methanesulfonamide

Suppliers and Price of N-[1-Morpholin-4-yl-1-phenyl-meth-(Z)-ylidene]-C-phenyl-methanesulfonamide

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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 N-[1-Morpholin-4-yl-1-phenyl-meth-(Z)-ylidene]-C-phenyl-methanesulfonamide

Chemical Property:

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Technology Process of N-[1-Morpholin-4-yl-1-phenyl-meth-(Z)-ylidene]-C-phenyl-methanesulfonamide

There total 1 articles about N-[1-Morpholin-4-yl-1-phenyl-meth-(Z)-ylidene]-C-phenyl-methanesulfonamide 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:

: 20474-37-7
benzylsulfonyl azide

: 7196-01-2
4-(1-phenylvinyl)morpholine

: 134772-64-8
N-[1-Morpholin-4-yl-1-phenyl-meth-(Z)-ylidene]-C-phenyl-methanesulfonamide

Guidance literature:: Yield given. Multistep reaction; anhydrous CH₂Cl₂, 2-3 h;
DOI:10.1016/S0040-4020(01)96105-8

Reference yield:

: 134772-64-8
N-[1-Morpholin-4-yl-1-phenyl-meth-(Z)-ylidene]-C-phenyl-methanesulfonamide

: 451-40-1
phenyl benzyl ketone

: 134772-73-9
3,4-Diphenyl-4H-[1,2]thiazete 1,1-dioxide

: 134772-77-3
2-Oxo-1,2-diphenyl-ethanesulfonic acid amide

: 134772-83-1
(Z)-2-Morpholin-4-yl-1,2-diphenyl-ethenesulfonic acid amide

Guidance literature:: With lithium diisopropyl amide; Yield given. Multistep reaction. Yields of byproduct given; 1.) anhydrous THF, -40 deg C, 2.) 12 h, room temperature;
DOI:10.1016/S0040-4020(01)96105-8