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N-Acetyl-2-phenylbut-2-ylamin, also known as 2-phenyl-N-acetylbutan-2-amine, is an organic compound with the molecular formula C12H17NO. It is a derivative of 2-phenylbutan-2-amine, where an acetyl group (CH3CO) is attached to the nitrogen atom. This chemical is a colorless to pale yellow liquid with a molecular weight of 191.27 g/mol. It is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain drugs and pesticides. Due to its potential applications in the chemical industry, it is important to handle N-Acetyl-2-phenylbut-2-ylamin with care, as it may have certain health and environmental implications.

4166-55-6

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4166-55-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4166-55-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,6 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4166-55:
(6*4)+(5*1)+(4*6)+(3*6)+(2*5)+(1*5)=86
86 % 10 = 6
So 4166-55-6 is a valid CAS Registry Number.

4166-55-6Relevant academic research and scientific papers

Catalytic oxidation of C-H bonds

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Page 7 - 8, (2008/06/13)

The invention provides a catalytic, chemospecific and stereospecific method of oxidizing a wide variety of substrates without unwanted side reactions. Essentially, the method of the instant invention, under relatively mild reaction conditions, catalytically, stereospecifically and chemospecifically inserts oxygen into a hydrocarbon C—H bond. Oxidation (oxygen insertion) at a tertiary C—H bond to form an alcohol (and in some cases a hemiacetal) at the tertiary carbon is favored. The stereochemistry of an oxidized tertiary carbon is preserved. Ketones are formed by oxidizing a secondary C—H bond and ring-cleaved diones are formed by oxidizing cis tertiary CH bonds.

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