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(2R,3R)-2,3-epoxy-3-phenyl-N-(R)-1phenylethylpropionamide is a complex organic compound with a molecular formula of C18H17NO2. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it is characterized by its specific stereochemistry, with the R configuration at both the 2 and 3 positions. The compound features an epoxy group, which is a three-membered ring consisting of two carbon atoms and one oxygen atom, and a phenyl group attached to the epoxy ring. Additionally, it has a propionamide group, which is an amide derived from propionic acid, and a phenylethyl group attached to the nitrogen atom. (2R,3R)-2,3-epoxy-3-phenyl-N-<(R)-1phenylethyl>propionamide is of interest in the field of organic chemistry and may have potential applications in pharmaceuticals or as a precursor in the synthesis of other complex molecules.

94160-93-7

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94160-93-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94160-93-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,1,6 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 94160-93:
(7*9)+(6*4)+(5*1)+(4*6)+(3*0)+(2*9)+(1*3)=137
137 % 10 = 7
So 94160-93-7 is a valid CAS Registry Number.

94160-93-7Upstream product

94160-93-7Downstream Products

94160-93-7Relevant academic research and scientific papers

ASYMMETRIC HYDROGENATION CATALYZED BY (ACHIRAL BASE)BIS(DIMETHYLGLYOXIMATO)COBALT(II)-CHIRAL COCATALYST SYSTEM.

Takeuchi,Ohgo

, p. 1920 - 1928 (1984)

Chiral tertiary amines with a secondary amide group at alpha - or beta -carbon were prepared, and an asymmetric hydrogenation of methyl 2-(acetylamino)acrylate and N,N prime -dimethyl-5-benzylidenehydantoin catalyzed by achiral base-coordinated bis(dimethylglyoximato)cobalt(II)-chiral cocatalyst system was examined by using each of them as the cocatalyst. The enantiomeric excess of N,N prime -dimethyl-5-benzylhydantoin reached 79. 1% with (S)-N- left bracket (R)-1-phenylethyl right bracket -2-quinuclidinecarboxamide as the cocatalyst. Remarkable differences were observed in the enantioselectivities between the two substrates for the same cocatalysts.

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