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2-(4-amino-3,5-dichlorophenyl)-N-(tert-butyl)-2-oxoacetamide is a complex organic compound with the molecular formula C11H12Cl2N2O2. It features a 2-oxoacetamide group, which is a derivative of acetamide with a carbonyl group, and a 4-amino-3,5-dichlorophenyl moiety, indicating the presence of a chlorine atom at the 3rd and 5th positions and an amino group at the 4th position on the phenyl ring. The tert-butyl group, a type of alkyl group, is attached to the nitrogen atom. 2-(4-amino-3,5-dichlorophenyl)-N-(tert-butyl)-2-oxoacetamide is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain herbicides. Its chemical structure and properties make it a versatile building block in organic synthesis, though it requires careful handling due to its potential reactivity and the presence of chlorine atoms, which can affect its stability and environmental impact.

75136-79-7

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75136-79-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75136-79-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,1,3 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75136-79:
(7*7)+(6*5)+(5*1)+(4*3)+(3*6)+(2*7)+(1*9)=137
137 % 10 = 7
So 75136-79-7 is a valid CAS Registry Number.

75136-79-7Downstream Products

75136-79-7Relevant academic research and scientific papers

Palladium-catalyzed double carbonylation using near stoichiometric carbon monoxide: Expedient access to substituted 13C2-labeled phenethylamines

Nielsen, Dennis U.,Neumann, Karoline,Taaning, Rolf H.,Lindhardt, Anders T.,Modvig, Amalie,Skrydstrup, Troels

experimental part, p. 6155 - 6165 (2012/09/21)

A novel and general approach for 13C2- and 2H-labeled phenethylamine derivatives has been developed, based on a highly convergent single-step assembly of the carbon skeleton. The efficient incorporation of two carbon-13 isotopes into phenethylamines was accomplished using a palladium-catalyzed double carbonylation of aryl iodides with near stoichiometric carbon monoxide.

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