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(R,S)-2-phenylacetamido-cyclohexanone is a chiral compound with the molecular formula C14H17NO2. It is a derivative of cyclohexanone, where one of the hydrogen atoms on the cyclohexane ring is replaced by a phenylacetamido group. (R,S)-2-phenylacetamido-cyclohexanone exists as a mixture of two enantiomers, R and S, which are non-superimposable mirror images of each other. The R and S designations refer to the absolute configuration of the chiral center, which in this case is the carbon atom attached to the phenyl group and the amide group. The compound is of interest in organic chemistry and pharmaceutical research due to its potential applications in the synthesis of various drugs and other bioactive molecules.

3270-67-5

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3270-67-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3270-67-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,7 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3270-67:
(6*3)+(5*2)+(4*7)+(3*0)+(2*6)+(1*7)=75
75 % 10 = 5
So 3270-67-5 is a valid CAS Registry Number.

3270-67-5Downstream Products

3270-67-5Relevant academic research and scientific papers

Asymmetric reductive amination of cycloalkanones, XIII: Enantioselective amidoamination: A new regiospecific strategy for the synthesis of chiral cyclohexane-1,2-diamino-derivatives

Schlichter,Frahm

, p. 429 - 436 (1993)

Asymmetric synthesis of trans- and cis-2-Benzamido- or 2-Phenyl-acetamido-cyclohexane-amines 7 and 8 by means of reductive amination and hydrogenolysis is described. Condensation of the amido-ketones 3 with chiral auxiliary (R)-(+) and (S)-(-)-1-phenylethylamine, respectively, leads to the amido-imines 4, which are hydrogenated over Raney-Ni to yield simultaneously enantiomerically pure secondary trans- and cis-2-amido-cyclohexane-amines 5 and 6.

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