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(R)-2-(N-methylacetamido)-2-phenylacetic acid is a chiral compound with the molecular formula C11H13NO3. It is a derivative of phenylacetic acid, featuring a methylacetamido group attached to the 2-position of the phenyl ring. (R)-2-(N-methylacetamido)-2-phenylacetic acid is known for its potential applications in pharmaceuticals, particularly as a building block for the synthesis of various drugs. Its chirality, indicated by the "R" prefix, signifies that it is the right-handed enantiomer, which is crucial for its biological activity and selectivity. The compound's structure and properties make it a valuable intermediate in the development of new medications, highlighting its importance in the field of medicinal chemistry.

2392-52-1

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2392-52-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2392-52-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,9 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2392-52:
(6*2)+(5*3)+(4*9)+(3*2)+(2*5)+(1*2)=81
81 % 10 = 1
So 2392-52-1 is a valid CAS Registry Number.

2392-52-1Downstream Products

2392-52-1Relevant academic research and scientific papers

Dynamic asymmetric multicomponent resolution: Lipase-mediated amidation of a double dynamic covalent system

Vongvilai, Pornrapee,Ramstroem, Olof

supporting information; experimental part, p. 14419 - 14425 (2010/02/16)

The Strecker reaction is one of the most important multicomponent reactions developed, leading to R-aminonitriles that are versatile substrates for many synthetic applications. In the present study, this reaction type has been applied to a double dynamic covalent resolution protocol, leading to efficient C-C- and C-N-bond generation as well as chiral discrimination. The combination of transimination with iminecyanation enabled the dynamic exchange in more than one direction around a single stereogenic center of restricted structure. This multiple exchange process could generate a vast range of compounds from a low number of starting materials in very short time. The resulting double dynamic covalent systems, created under thermodynamic control, were subsequently coupled in a one-pot process with kinetically controlled lipase-mediated transacylation. This resulted in complete resolution of the dynamic systems, yielding the optimal N-acyl-α-aminonitriles for the enzyme, where the individual chemoenzymatic reactions could produce enantiomerically pure acylated N-substituted α-aminonitriles in good yields.

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