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139109-23-2

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139109-23-2 Usage

General Description

"(4R,5S)-1,5-dimethyl-4-phenyl-3-(2-propenoyl)-2-imidazolidinone" is a chemical compound composed of a 4-phenyl-2-imidazolidinone ring with a 1,5-dimethyl substitution and a 2-propenoyl group attached to the nitrogen atom. (4R,5S)-1,5-dimethyl-4-phenyl-3-(2-propenoyl)-2-imidazolidinone is a chiral molecule with a specific 4R,5S configuration. It may have potential applications in pharmaceuticals or as a building block for synthesizing other organic compounds. The 2-imidazolidinone core is commonly found in various biologically active molecules, and the presence of a 2-propenoyl group could confer additional reactivity and functionality to the compound, making it a valuable starting material for chemical synthesis. The specific stereochemistry of this compound could also impact its potential biological activity and interactions with other molecules. Overall, "(4R,5S)-1,5-dimethyl-4-phenyl-3-(2-propenoyl)-2-imidazolidinone" is a complex and potentially valuable chemical entity with a range of potential applications in the fields of chemistry and medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 139109-23-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,1,0 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 139109-23:
(8*1)+(7*3)+(6*9)+(5*1)+(4*0)+(3*9)+(2*2)+(1*3)=122
122 % 10 = 2
So 139109-23-2 is a valid CAS Registry Number.

139109-23-2Relevant articles and documents

N-Alkenoylimidazolidin-2-ones as chiral dienophiles in Diels-Alder cycloaddition reactions

Roos, Gregory H. P.,Kriel, Karina N.,Emslie, Neville D.,Balasubramaniam, Sundari

, p. 104 - 112 (2007/10/03)

Homochiral N-enoylimidazolidin-2-ones 5-8 are readily accessible, practical, and highly diastereoselective dienophiles in dialkylaluminium-promoted Diels-Alder reactions. Acrylate, methacrylate, and (E)-crotonate derivatives bearing ephedrine-based imidaz

A novel method for the N-acylation of (4R,5S)-1,5-dimethyl-4-phenylimidazolidin-2-one

Kriel, Karina N.,Emslie, Neville D.,Roost, Gregory H. P.

, p. 109 - 110 (2007/10/03)

An efficient synthesis of N-Acylimidazolidinones derived from α,β-unsaturated acid chlorides using DABCO as the base is described.

Imidazolidin-2-ones as Practical, Efficient Chiral Auxiliaries in Diels-Alder Reactions

Jensen, Karina N.,Roos, Gregory H. P.

, p. 1553 - 1554 (2007/10/02)

The readily prepared (4R,5S)-1,5-dimethyl-4-phenylimidazolidin-2-one and its 4-cyclohexyl analogue proved to be very powerful face-selective auxiliaries in catalysed Diels-Alder cycloadditions of their α,β-unsaturated N-acyl dienophile derivatives.

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