3-(3',5'-Dibromo-2'-methoxyphenyl)-2-isocyano-2-propenoic Acid Methyl Ester

Base Information

Chemical Name:3-(3',5'-Dibromo-2'-methoxyphenyl)-2-isocyano-2-propenoic Acid Methyl Ester
CAS No.:133871-72-4
Molecular Formula:C₁₂H₉Br₂NO₃
Molecular Weight:375.016
Hs Code.:

Synonyms:3-(3',5'-Dibromo-2'-methoxyphenyl)-2-isocyano-2-propenoic Acid Methyl Ester

Suppliers and Price of 3-(3',5'-Dibromo-2'-methoxyphenyl)-2-isocyano-2-propenoic Acid Methyl Ester

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 3-(3',5'-Dibromo-2'-methoxyphenyl)-2-isocyano-2-propenoic Acid Methyl Ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 3-(3',5'-Dibromo-2'-methoxyphenyl)-2-isocyano-2-propenoic Acid Methyl Ester

There total 2 articles about 3-(3',5'-Dibromo-2'-methoxyphenyl)-2-isocyano-2-propenoic Acid Methyl 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: 80.0%

: 133886-89-2
3-(3',5'-Dibromo-2'-methoxyphenyl)-2-formamido-2-propenoic Acid Methyl Ester

: 133871-72-4
3-(3',5'-Dibromo-2'-methoxyphenyl)-2-isocyano-2-propenoic Acid Methyl Ester

Guidance literature:: With triethylamine; trichlorophosphate; In dichloromethane; for 3h; Ambient temperature;

Reference yield:

: 61657-65-6
3,5-dibromo-2-methoxybenzaldehyde

: 133871-72-4
3-(3',5'-Dibromo-2'-methoxyphenyl)-2-isocyano-2-propenoic Acid Methyl Ester

Guidance literature:: Multi-step reaction with 2 steps

1: 55 percent / potassium tert-butanolate / tetrahydrofuran / 12 h / Ambient temperature

2: 80 percent / triethylamine, phosphoryl chloride / CH₂Cl₂ / 3 h / Ambient temperature

With potassium tert-butylate; triethylamine; trichlorophosphate; In tetrahydrofuran; dichloromethane;