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(1'R,2'S,2S)-N,2-Dimethyl-N-(2'-hydroxy-1'-methyl-2'-phenylethyl)-3-<(tert-butyldimethylsilyl)oxy>propionamide is a complex organic compound with a molecular formula of C22H37NO3Si. It is a chiral molecule, meaning it has a non-superimposable mirror image, and is characterized by its specific stereochemistry: 1'R, 2'S, and 2S configurations. The compound features a propionamide group, which is an amide derived from propionic acid, and a tert-butyldimethylsilyl (TBDMS) group, a common protecting group in organic synthesis. The hydroxy group and the phenylethyl moiety contribute to its structural complexity. (1'R,2'S,2S)-N,2-Dimethyl-N-(2'-hydroxy-1'-methyl-2'-phenylethyl)-3-<(tert-butyldimethylsilyl)oxy>propionamide is likely used in advanced chemical synthesis, particularly in the preparation of pharmaceuticals or other specialty chemicals, where its unique structure and properties can be exploited for specific reactions or to achieve desired product selectivity.

93454-86-5

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93454-86-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93454-86-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,4,5 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 93454-86:
(7*9)+(6*3)+(5*4)+(4*5)+(3*4)+(2*8)+(1*6)=155
155 % 10 = 5
So 93454-86-5 is a valid CAS Registry Number.

93454-86-5Relevant academic research and scientific papers

Enantioselective Processes. Reaction of Optically Active Amines with Photochemically Generated Ketenes

Schultz, Arthur G.,Kulkarni, Yashwant S.

, p. 5202 - 5206 (2007/10/02)

The diastereoselectivity of the reaction of d- and l-ephedrine with ketenes photochemically generated from 6-(2-oxopropyl)-2,4,6-trimethyl-2,4-cyclohexadien-1-one (1a), 6-(2-oxopropyl)-2,6-dimethyl-2,4-cyclohexadien-1-one (1b), and 6-acetoxy-2,4,6-trimethyl-2,4-cyclohexadien-1-one (3a) is described.Configurational assignments at C(2) in the major products 5a and 6 resulting from irradiation of 1a in the presence of d-ephedrine and l-ephedrine, respectively, were made by chemical degradation and correlation studies with (S)-(+)-3-hydroxy-2-methylpropanoic acid (7a).

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