91733-75-4 Usage
Uses
Used in Pharmaceutical Industry:
2-CBZ-AMINO-INDAN-2-CARBOXYLIC ACID is used as a key intermediate in the synthesis of new drugs for various therapeutic applications. Its unique structure allows for the development of molecules with specific biological activities, targeting a range of diseases and conditions.
Used in Organic Synthesis:
In the field of organic synthesis, 2-CBZ-AMINO-INDAN-2-CARBOXYLIC ACID serves as a versatile building block for the creation of complex organic molecules. Its functional groups can be selectively modified to generate a variety of derivatives with tailored properties.
Used in Medicinal Chemistry:
2-CBZ-AMINO-INDAN-2-CARBOXYLIC ACID is utilized in medicinal chemistry for the design and optimization of drug candidates. Its structural features can be exploited to enhance the potency, selectivity, and pharmacokinetic properties of potential therapeutic agents.
Further research and exploration of 2-CBZ-AMINO-INDAN-2-CARBOXYLIC ACID's properties and potential applications are necessary to fully understand its capabilities and limitations, paving the way for its integration into various industries and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 91733-75-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,7,3 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 91733-75:
(7*9)+(6*1)+(5*7)+(4*3)+(3*3)+(2*7)+(1*5)=144
144 % 10 = 4
So 91733-75-4 is a valid CAS Registry Number.
91733-75-4Relevant academic research and scientific papers
Leucine enkephalin analogues containing a conformationally restained N-terminal amino acid residue
Deeks,Crooks,Waigh
, p. 457 - 460 (2007/10/02)
Three analogues of leucine enkephalin, in which the terminal tyrosine-1 residue has been replaced by conformationally restrained aromatic amino acids, have been synthesized by classical solution methods. Their opiate agonist potencies on electrically stimulated guinea pig ileum and mouse vas deferens preparations were determined and compared with morphine, metenkephalin, and Leu enkephalin. None of these analogues had analgesic properties when evaluated on the above tissue preparations or when evaluated by the hot-plate test in mice after subcutaneous and intracerebroventricular administration.
