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N-o-tolyl-formimidic acid ethyl ester is an organic compound with the chemical formula C10H13NO2. It is a derivative of formimidic acid, featuring an ethyl ester group and an o-tolyl (2-methylphenyl) substituent. N-o-tolyl-formimidic acid ethyl ester is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain pesticides and drugs. Its chemical structure allows for further functionalization and modification, making it a versatile building block in organic synthesis. The compound is typically synthesized through the reaction of o-tolyl-formimidic acid with ethanol in the presence of an acid catalyst. It is important to handle N-o-tolyl-formimidic acid ethyl ester with care due to its potential reactivity and the need to adhere to safety protocols in a laboratory setting.

4943-59-3

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4943-59-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4943-59-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,4 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4943-59:
(6*4)+(5*9)+(4*4)+(3*3)+(2*5)+(1*9)=113
113 % 10 = 3
So 4943-59-3 is a valid CAS Registry Number.

4943-59-3Relevant academic research and scientific papers

Multicomponent synthesis of 1-aryl 1,2,4-triazoles

Tam, Annie,Armstrong, Ian S.,La Cruz, Thomas E.

supporting information, p. 3586 - 3589 (2013/08/23)

A multicomponent (single reactor) process for the synthesis of 1-aryl 1,2,4-triazoles was explored and developed. This transformation prepared the 1,2,4-triazole directly from anilines, amino pyridines, and pyrimidines. The reaction scope was explored with 21 different substrates, and the position of the nitrogen atoms in the newly formed ring was established by 15N labeling and NMR spectroscopy.

A facile protocol for the synthesis of mono-N-methyl anilines via formimidate intermediates

Sun, Nan,Wang, Shuai,Mo, Weimin,Hu, Baoxiang,Shen, Zhenlu,Hu, Xinquan

experimental part, p. 7142 - 7148 (2010/09/14)

A general procedure for the preparation of mono-N-methyl anilines has been developed with excellent yields. This protocol relies on a NaBH3(OAc) reduction of formimidate intermediates that are quantitatively generated by treatment of primary substituted anilines with triethyl orthoformate under the catalysis of MCM-41-SO3H mesoporous zeolite. The newly developed procedure was facile, efficient, and environmentally benign.

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