261165-16-6 Usage
Description
(R,S)-N-(1,1-dimethylethoxycarbonyl)-2,5-difluorophenylalanine is a chiral phenylalanine derivative that possesses two enantiomers, (R)and (S)-N-(1,1-dimethylethoxycarbonyl)-2,5-difluorophenylalanine. This chemical compound is characterized by its unique structure, which includes a difluorophenylalanine moiety that can impart distinct properties and functions to the molecules it is a part of. As a result, it plays a significant role in the synthesis of pharmaceuticals and biologically active compounds, making it a valuable building block in the development of novel drugs and chemical entities.
Uses
Used in Pharmaceutical Synthesis:
(R,S)-N-(1,1-dimethylethoxycarbonyl)-2,5-difluorophenylalanine is used as a key intermediate in the pharmaceutical industry for the synthesis of various drugs and biologically active molecules. The presence of the difluorophenylalanine group in its structure allows for the creation of compounds with enhanced properties, such as improved potency, selectivity, or stability.
Used in Organic Chemistry Research:
In the field of organic chemistry, (R,S)-N-(1,1-dimethylethoxycarbonyl)-2,5-difluorophenylalanine serves as an important building block for the development of new chemical compounds. Its unique structure enables researchers to explore novel reactions and synthetic pathways, leading to the discovery of innovative molecules with potential applications in various industries.
Used in Drug Design and Development:
(R,S)-N-(1,1-dimethylethoxycarbonyl)-2,5-difluorophenylalanine is utilized in drug design and development as a structural element that can be incorporated into new drug candidates. Its unique properties can contribute to the optimization of drug candidates, potentially improving their pharmacokinetic and pharmacodynamic profiles, as well as their overall efficacy and safety.
Used in the Synthesis of Chiral Compounds:
Due to its chiral nature, (R,S)-N-(1,1-dimethylethoxycarbonyl)-2,5-difluorophenylalanine is also used in the synthesis of chiral compounds, which are essential in various applications, including pharmaceuticals, agrochemicals, and materials science. The ability to control the stereochemistry of this compound can lead to the development of enantiomerically pure products with specific biological activities.
Check Digit Verification of cas no
The CAS Registry Mumber 261165-16-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,1,1,6 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 261165-16:
(8*2)+(7*6)+(6*1)+(5*1)+(4*6)+(3*5)+(2*1)+(1*6)=116
116 % 10 = 6
So 261165-16-6 is a valid CAS Registry Number.
261165-16-6Relevant articles and documents
PHENYL COMPOUNDS
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Page/Page column 37-38, (2010/11/25)
The present invention is directed to compounds of formula (I) or a pharmaceutically acceptable salt thereof; wherein A is (xx) ; X is selected from CH, CF and N, R5 is selected from H, C1-C6 alkyl, C1-C6 fluoroa
