53984-75-1 Usage
Description
(2S)-N-(2,6-Dimethylphenyl)-2-aminopropanamide is a chiral compound with a molecular formula of C11H16N2O. It is a synthetic derivative of the amino acid alanine, featuring a 2,6-dimethylphenyl group. (2S)-N-(2,6-Dimethylphenyl)-2-aminopropanamide holds potential in medicinal chemistry as a building block for the synthesis of pharmaceuticals and biologically active molecules.
Uses
Used in Pharmaceutical Industry:
(2S)-N-(2,6-Dimethylphenyl)-2-aminopropanamide is used as a building block for the synthesis of pharmaceuticals due to its unique chemical structure and potential biological properties. It contributes to the development of new drugs and therapies, enhancing the range of available treatments.
Used in Research and Development:
In the field of research and development, (2S)-N-(2,6-Dimethylphenyl)-2-aminopropanamide is utilized for the study of chiral compounds and their biological activities. Its unique stereochemistry allows for the exploration of the effects of chirality on biological systems and the discovery of novel therapeutic agents.
Used in Medicinal Chemistry:
(2S)-N-(2,6-Dimethylphenyl)-2-aminopropanamide is employed as a key component in the design and synthesis of biologically active molecules. Its incorporation into various chemical structures can lead to the creation of new compounds with specific therapeutic effects, broadening the scope of medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 53984-75-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,9,8 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 53984-75:
(7*5)+(6*3)+(5*9)+(4*8)+(3*4)+(2*7)+(1*5)=161
161 % 10 = 1
So 53984-75-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H16N2O/c1-7-5-4-6-8(2)10(7)13-11(14)9(3)12/h4-6,9H,12H2,1-3H3,(H,13,14)/t9-/m0/s1
53984-75-1Relevant articles and documents
Liquid chromatographic resolution of tocainide and its analogues on a doubly tethered chiral stationary phase based on (+)-(18-Crown-6)-2,3,11,12- tetracarboxylic acid
Kim, Hee Jin,Choi, Hee Jung,Hyun, Myung Ho
experimental part, p. 678 - 682 (2010/08/07)
A doubly tethered chiral stationary phase (CSP) based on (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid were applied to the liquid chromatographic resolution of racemic tocainide, an antiarrhythmic agent, and its analogues. The chiral recognition efficiency of the doubly tethered CSP for tocainide and its analogues was generally greater than that of the corresponding singly tethered CSP especially in terms of the resolution (RS). The resolution of tocainide and its analogues on the doubly tethered CSP were dependent on the content and the type of the organic and acidic modifiers in aqueous mobile phase and the column temperature. Especially, the retention behaviors of analytes on the doubly tethered CSP with the variation of the content of organic modifier in aqueous mobile phase were opposite to those on the corresponding singly tethered CSP and these opposite retention behaviors were rationalized by the lipophilicity differences of the two CSPs.
The mode of action of local anesthetics. 7. Synthesis of enantiomeric N-aminoacyl-2.6.-dimethylaniline, -benzylamine and-2-phenylethylamine
Schoenenberger,Endres
, p. 30 - 32,31,32 (2007/10/06)
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