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N-Benzyl-1-phenyl-cyclohexylamin is a complex organic compound with the molecular formula C23H25N. It is a derivative of cyclohexylamine, where one hydrogen atom is replaced by a benzyl group and a phenyl group. N-Benzyl-1-phenyl-cyclohexylamin is characterized by its cyclic structure, with a cyclohexane ring as the central core, and is known for its potential applications in the synthesis of various pharmaceuticals and chemical intermediates. The presence of both benzyl and phenyl groups contributes to its unique chemical properties, making it a versatile building block in organic chemistry.

2201-51-6

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2201-51-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2201-51-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,0 and 1 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2201-51:
(6*2)+(5*2)+(4*0)+(3*1)+(2*5)+(1*1)=36
36 % 10 = 6
So 2201-51-6 is a valid CAS Registry Number.

2201-51-6Downstream Products

2201-51-6Relevant academic research and scientific papers

Metabolism of phencyclidine. The role of the carbinolamine intermediate in the formation of lactam and amino acid metabolites of nitrogen heterocycles

Baker,Little

, p. 46 - 50 (1985)

The transformation of phencyclidine in a mouse liver microsome preparation to several oxidative metabolites was studied. With use of GLC and HPLC methods with internal standards, phencyclidine and six metabolites were quantitated and the amino acid, resulting from the α-oxidation of the piperidine ring, was produced in 10-50 times greater amounts than the other metabolites. While most piperidines and pyrrolidines produce an amino acid and a corresponding lactam, it was found that phencyclidine was not converted to the lactam.

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