4-Nitro-benzoic acid 3,5-dichloro-2-{[1-ethoxycarbonyl-meth-(E)-ylidene]-amino}-phenyl ester

Base Information

Chemical Name:4-Nitro-benzoic acid 3,5-dichloro-2-{[1-ethoxycarbonyl-meth-(E)-ylidene]-amino}-phenyl ester
CAS No.:100190-02-1
Molecular Formula:C₁₇H₁₂Cl₂N₂O₆
Molecular Weight:411.198
Hs Code.:

Synonyms:4-Nitro-benzoic acid 3,5-dichloro-2-{[1-ethoxycarbonyl-meth-(E)-ylidene]-amino}-phenyl ester

Suppliers and Price of 4-Nitro-benzoic acid 3,5-dichloro-2-{[1-ethoxycarbonyl-meth-(E)-ylidene]-amino}-phenyl ester

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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-Nitro-benzoic acid 3,5-dichloro-2-{[1-ethoxycarbonyl-meth-(E)-ylidene]-amino}-phenyl ester

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Technology Process of 4-Nitro-benzoic acid 3,5-dichloro-2-{[1-ethoxycarbonyl-meth-(E)-ylidene]-amino}-phenyl ester

There total 2 articles about 4-Nitro-benzoic acid 3,5-dichloro-2-{[1-ethoxycarbonyl-meth-(E)-ylidene]-amino}-phenyl ester 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:

: 7380-81-6
ethyl (dimethylsulfuranylidene)acetate

: 90388-37-7
N-(2,4-dichloro-6-oxo-2,4-cyclohexadien-1-ylidene)-4-nitrobenzamide

: 100190-02-1
4-Nitro-benzoic acid 3,5-dichloro-2-{[1-ethoxycarbonyl-meth-(E)-ylidene]-amino}-phenyl ester

Guidance literature:: In dichloromethane;
DOI:10.1021/jo00356a014

Reference yield:

: 623-73-4
diazoacetic acid ethyl ester

: 90388-37-7
N-(2,4-dichloro-6-oxo-2,4-cyclohexadien-1-ylidene)-4-nitrobenzamide

: 100190-02-1
4-Nitro-benzoic acid 3,5-dichloro-2-{[1-ethoxycarbonyl-meth-(E)-ylidene]-amino}-phenyl ester

Guidance literature:: In dichloromethane; for 4h; Mechanism; Ambient temperature; other diazoalkanes and o-quinone monoimides;
DOI:10.1021/jo00356a014