Methyl N-(3,4-dichlorophenyl)-alpha-oxobenzeneethanimidate

Base Information

Chemical Name:Methyl N-(3,4-dichlorophenyl)-alpha-oxobenzeneethanimidate
CAS No.:79807-39-9
Molecular Formula:C₁₅H₁₁Cl₂NO₂
Molecular Weight:308.164
Hs Code.:
DSSTox Substance ID:DTXSID001207544

Synonyms:Methyl N-(3,4-dichlorophenyl)-alpha-oxobenzeneethanimidate;DTXSID001207544;79807-39-9

Suppliers and Price of Methyl N-(3,4-dichlorophenyl)-alpha-oxobenzeneethanimidate

Supply Marketing:

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

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Chemical Property of Methyl N-(3,4-dichlorophenyl)-alpha-oxobenzeneethanimidate

Chemical Property:

XLogP3:4.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:307.0166840
Heavy Atom Count:20
Complexity:367

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC(=NC1=CC(=C(C=C1)Cl)Cl)C(=O)C2=CC=CC=C2

Technology Process of Methyl N-(3,4-dichlorophenyl)-alpha-oxobenzeneethanimidate

There total 6 articles about Methyl N-(3,4-dichlorophenyl)-alpha-oxobenzeneethanimidate 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: 75.0%

: 79866-26-5
3,4-dichloro-N-(α-methoxyphenacyl)-N-tosylaniline

: 79807-39-9
methyl N-(3,4-dichlorophenyl)benzoylcarboximidate

Guidance literature:: With sodium methylate; In methanol; 1.) reflux, 3 h, 2.) room temperature, overnight;
DOI:10.1039/P19810002435

Reference yield:

: 6956-56-5
2,2-dimethoxy-1-phenylethanone

: 79807-39-9
methyl N-(3,4-dichlorophenyl)benzoylcarboximidate

Guidance literature:: Multi-step reaction with 3 steps

1: 91 percent / 0.25 h / Heating

2: 56 percent / K₂CO₃ / acetone / 24 h / Heating

3: 75 percent / sodium methoxide / methanol / 1.) reflux, 3 h, 2.) room temperature, overnight

With sodium methylate; potassium carbonate; In methanol; acetone;
DOI:10.1039/P19810002435

Reference yield:

: 21160-29-2
a-bromo-1-methoxyacetophenone

: 79807-39-9
methyl N-(3,4-dichlorophenyl)benzoylcarboximidate

Guidance literature:: Multi-step reaction with 2 steps

1: 56 percent / K₂CO₃ / acetone / 24 h / Heating

2: 75 percent / sodium methoxide / methanol / 1.) reflux, 3 h, 2.) room temperature, overnight

With sodium methylate; potassium carbonate; In methanol; acetone;
DOI:10.1039/P19810002435