886363-59-3 Usage
Uses
Used in Pharmaceutical Industry:
(4-N-BOC-AMINO-PIPERIDIN-1-YL)-PHENYL-ACETIC ACID is used as a key intermediate in the synthesis of various drug molecules due to its unique structural features and reactivity. The BOC protecting group ensures that the amino group remains unreactive until specifically deprotected, allowing for precise control over the chemical reactions involved in drug synthesis.
Used in Drug Development:
In the realm of drug development, (4-N-BOC-AMINO-PIPERIDIN-1-YL)-PHENYL-ACETIC ACID is utilized as a precursor for the creation of pharmaceutical agents with a wide range of biological activities. Its lipophilic nature, conferred by the phenylacetic acid component, aids in the compound's ability to interact with biological targets, potentially leading to the discovery of new therapeutic agents.
Used in Medicinal Chemistry Research:
(4-N-BOC-AMINO-PIPERIDIN-1-YL)-PHENYL-ACETIC ACID serves as a valuable tool in medicinal chemistry research, where it can be employed to explore the structure-activity relationships of potential drug candidates. (4-N-BOC-AMINO-PIPERIDIN-1-YL)-PHENYL-ACETIC ACID's modular nature allows for systematic variation of its structure to optimize pharmacological properties such as potency, selectivity, and pharmacokinetics.
Check Digit Verification of cas no
The CAS Registry Mumber 886363-59-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,6,3,6 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 886363-59:
(8*8)+(7*8)+(6*6)+(5*3)+(4*6)+(3*3)+(2*5)+(1*9)=223
223 % 10 = 3
So 886363-59-3 is a valid CAS Registry Number.
InChI:InChI=1/C18H26N2O4/c1-18(2,3)24-17(23)19-14-9-11-20(12-10-14)15(16(21)22)13-7-5-4-6-8-13/h4-8,14-15H,9-12H2,1-3H3,(H,19,23)(H,21,22)
