14429-43-7 Usage
Uses
Given the limited information available on (R)-Acetylamino-cyclohexyl-acetic acid, its uses are speculative and would require further research for a comprehensive understanding. However, based on its classification as an amino acid derivative, potential applications could be explored in the following areas:
Used in Pharmaceutical Industry:
(R)-Acetylamino-cyclohexyl-acetic acid could be utilized as a building block for the synthesis of pharmaceutical compounds, given the importance of amino acids in drug development. Its unique structure may offer novel properties that could be harnessed for the creation of new therapeutic agents.
Used in Chemical Research:
In the field of chemical research, (R)-Acetylamino-cyclohexyl-acetic acid may serve as a subject for studies on chirality, stereochemistry, and the exploration of its reactivity with other chemical entities. Understanding its behavior could contribute to the broader knowledge of amino acid derivatives and their potential applications.
Used in Material Science:
(R)-ACETYLAMINO-CYCLOHEXYL-ACETIC ACID's structural features might also make it a candidate for material science applications, where its properties could be investigated for use in the development of new materials with specific characteristics, such as chiral catalysts or enantioselective sensors.
Check Digit Verification of cas no
The CAS Registry Mumber 14429-43-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,4,2 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 14429-43:
(7*1)+(6*4)+(5*4)+(4*2)+(3*9)+(2*4)+(1*3)=97
97 % 10 = 7
So 14429-43-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H17NO3/c1-7(12)11-9(10(13)14)8-5-3-2-4-6-8/h8-9H,2-6H2,1H3,(H,11,12)(H,13,14)/t9-/m1/s1
14429-43-7Relevant academic research and scientific papers
IMIDAZOTRIAZINONE DERIVATIVES AS PDE 7 (PHOSPHODIESTERASE 7) INHIBITORS
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Page/Page column 20, (2010/02/10)
The present invention provides the compounds inhibiting PDE 7 selectively, and therefore, enhances cellular cAMP level. Consequently, the compound is useful for treating various kinds of disease such as allergic disease, inflammatory disease or immunologi
Efficient chemoenzymatic synthesis of enantiomerically pure α-amino acids
Beller, Matthias,Eckert, Markus,Geissler, Holger,Napierski, Bernd,Rebenstock, Heinz-Peter,Holla, E. Wolfgang
, p. 935 - 941 (2007/10/03)
A general two-step chemoenzymatic synthesis for enantiomerically pure natural and nonnatural α-amino acids is presented. In the first step of the sequence, the ubiquitous educts aldehyde, amide and carbon monoxide react by palladium-catalyzed amidocarbonylation to afford the racemic N-acyl amino acids in excellent yields. In the second step, enzymatic enantioselective hydrolysis yields the free optically pure a-amino acid and the other enantiomer as the N-acyl derivative, both in optical purities of 85-99.5% ee. The advantage of the chemoenzymatic process compared to other amino acid synthesis are demonstrated by the preparation of various functionalized (-OR, -Cl, -F, -SR) α-amino acids on a 10-g scale.
