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(1'R,2'S,2S)-N-(2'-Hydroxy-1'-methyl-2'-phenylethyl)-8-oxo-N,2,6-trimethylnona-3,5-dienamide is a complex organic compound with a molecular formula of C21H29NO3. It is a chiral molecule, meaning it has a non-superimposable mirror image, and is characterized by its specific stereochemistry at the 1', 2', and 2S positions. (1'R,2'S,2S)-N-(2'-Hydroxy-1'-methyl-2'-phenylethyl)-8-oxo-N,2,6-trimethylnona-3,5-dienamide features a hydroxyl group, a methyl group, and a phenyl group attached to a central carbon chain, which is part of a larger amide structure. The 8-oxo group indicates the presence of a carbonyl group at the 8th position, and the N,2,6-trimethyl groups suggest three methyl groups attached to the nitrogen and two carbon atoms of the nona-3,5-dienamide backbone. This chemical structure is significant in the field of organic chemistry and may have potential applications in pharmaceuticals or other industries due to its unique properties and reactivity.

93454-83-2

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93454-83-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93454-83-2 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 93454-83:
(7*9)+(6*3)+(5*4)+(4*5)+(3*4)+(2*8)+(1*3)=152
152 % 10 = 2
So 93454-83-2 is a valid CAS Registry Number.

93454-83-2Downstream Products

93454-83-2Relevant 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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