61865-62-1 Usage
Description
(1S,4R)-4-AMINO-CYCLOPENT-2-ENECARBOXYLIC ACID HYDROCHLORIDE is a cyclopentane derivative featuring an amino group. It is commonly utilized as a building block in the synthesis of pharmaceutical compounds, with the hydrochloride salt form providing stability and water solubility for research and industrial applications. (1S,4R)-4-AMINO-CYCLOPENT-2-ENECARBOXYLIC ACID HYDROCHLORIDE may also have potential in the development of new drugs or as a reagent in organic synthesis, necessitating proper safety handling and adherence to laboratory best practices.
Uses
Used in Pharmaceutical Synthesis:
(1S,4R)-4-AMINO-CYCLOPENT-2-ENECARBOXYLIC ACID HYDROCHLORIDE is used as a building block for the synthesis of various pharmaceutical compounds, contributing to the development of new drugs and therapeutic agents.
Used in Organic Synthesis:
(1S,4R)-4-AMINO-CYCLOPENT-2-ENECARBOXYLIC ACID HYDROCHLORIDE is used as a reagent in organic synthesis, facilitating the creation of complex organic molecules and contributing to advancements in chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 61865-62-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,8,6 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 61865-62:
(7*6)+(6*1)+(5*8)+(4*6)+(3*5)+(2*6)+(1*2)=141
141 % 10 = 1
So 61865-62-1 is a valid CAS Registry Number.
61865-62-1Relevant articles and documents
Synthesis of cyclic γ-amino acids for foldamers and peptide nanotubes
Rodriguez-Vazquez, Nuria,Salzinger, Stephan,Silva, Luis F.,Amorin, Manuel,Granja, Juan R.
, p. 3477 - 3493 (2013/07/11)
Cyclic γ-amino acids are molecular building blocks of great interest in peptide and foldamer chemistry, as they allow the preparation of new structures that are not found in Nature. In this paper, we describe the synthesis of cyclic γ-amino acids that have a cis relationship between the amino and the carboxylic acid groups. This arrangement, in most cases, induces the resulting peptides to adopt a flat conformation, which makes them appropriate for the design of foldamers that adopt β-sheet-type structures. We describe the synthesis of cyclic γ-amino acids that have a cis relationship between the amino and the carboxylic acid groups. This makes them suitable for the design of foldamers that adopt β-sheet-type structures.
