245115-20-2 Usage
Uses
Used in Pharmaceutical Research:
Cyclopentanecarboxylic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, ethyl ester, (1R,2R)is used as a chiral building block for the synthesis of various pharmaceutical compounds. Its unique stereochemistry allows for the creation of enantiomerically pure drugs, which can exhibit different biological activities and reduce potential side effects associated with racemic mixtures.
Used in Chemical Research:
In the field of chemical research, Cyclopentanecarboxylic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, ethyl ester, (1R,2R)serves as a versatile intermediate for the synthesis of complex organic molecules. Its reactivity and functional groups enable the formation of a wide range of chemical products, including agrochemicals, fragrances, and other specialty chemicals.
Used in Drug Development:
Cyclopentanecarboxylic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, ethyl ester, (1R,2R)is used as a potential candidate for drug development, particularly in the discovery of novel therapeutic agents. Its unique structure and chirality may contribute to the design of new drugs with improved efficacy, selectivity, and reduced side effects.
Used in Chiral Synthesis:
In the field of chiral synthesis, Cyclopentanecarboxylic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, ethyl ester, (1R,2R)is employed as a key chiral intermediate for the preparation of enantiomerically pure compounds. Its specific stereochemistry allows for the selective synthesis of target molecules with desired biological activities, which is crucial for the development of effective and safe pharmaceuticals.
Used in Analytical Chemistry:
Cyclopentanecarboxylic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, ethyl ester, (1R,2R)is utilized as a chiral reference standard in analytical chemistry. Its well-defined stereochemistry makes it an ideal compound for the calibration of chiral chromatographic methods and the determination of enantiomeric purity in various samples.
Check Digit Verification of cas no
The CAS Registry Mumber 245115-20-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,5,1,1 and 5 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 245115-20:
(8*2)+(7*4)+(6*5)+(5*1)+(4*1)+(3*5)+(2*2)+(1*0)=102
102 % 10 = 2
So 245115-20-2 is a valid CAS Registry Number.
245115-20-2Relevant academic research and scientific papers
Appella, Daniel H.,Christianson, Laurie A.,Klein, Daniel A.,Richards, Michele R.,Powell, Douglas R.,Gellman, Samuel H.
, p. 7574 - 7581 (1999)
Synthetic protocols and circular dichroism (CD) spectra are reported for a series of oligomers of (R,R)-trans-2-aminocyclopentanecarboxylic acid (trans-ACPC). The two longest oligomers, a hexamer and an octamer, have also been examined crystallographicall
