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(S)-2-(N-methylacetamido)-2-phenylacetic acid, also known as (S)-α-methyldopa or (S)-α-MD, is a chiral compound with the molecular formula C10H13NO3. It is a synthetic amino acid derivative that is primarily used as an antihypertensive agent in the treatment of hypertension. The compound is characterized by its (S)-configuration, which refers to the spatial arrangement of the molecule's atoms. It works by being metabolized in the body to produce α-methylnorepinephrine, which acts as a false neurotransmitter, reducing the release of norepinephrine and subsequently lowering blood pressure. (S)-2-(N-methylacetamido)-2-phenylacetic acid is an important pharmaceutical agent due to its effectiveness in managing high blood pressure and its role in the sympathetic nervous system.

2392-53-2

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2392-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2392-53-2 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 2392-53:
(6*2)+(5*3)+(4*9)+(3*2)+(2*5)+(1*3)=82
82 % 10 = 2
So 2392-53-2 is a valid CAS Registry Number.

2392-53-2Relevant 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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