1212153-95-1 Usage
Description
(2S,4S)-4-FMoc-aMino Pyrrolidine-2-carboxylic acid Methylester-HCl is a proline derivative featuring a pyrrolidine ring and a methylester group, existing as a hydrochloride salt. It is widely utilized in organic synthesis and medicinal chemistry as a key building block for the development of pharmaceuticals and bioactive compounds. The incorporation of the FMoc protecting group renders it highly suitable for solid-phase peptide synthesis, allowing for the creation of synthetic peptides through deprotection and combination with other amino acids. Additionally, this chemical is frequently employed in the research and development of novel drugs, particularly in the design of enzyme inhibitors and receptor ligands.
Uses
Used in Organic Synthesis:
(2S,4S)-4-FMoc-aMino Pyrrolidine-2-carboxylic acid Methylester-HCl is used as a building block in organic synthesis for the preparation of pharmaceuticals and bioactive compounds, due to its unique molecular structure and functional groups.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (2S,4S)-4-FMoc-aMino Pyrrolidine-2-carboxylic acid Methylester-HCl is used as a key component in the design and synthesis of new drugs, particularly enzyme inhibitors and receptor ligands, leveraging its versatile chemical properties and the presence of the FMoc protecting group.
Used in Solid-Phase Peptide Synthesis:
(2S,4S)-4-FMoc-aMino Pyrrolidine-2-carboxylic acid Methylester-HCl is used as a protected amino acid in solid-phase peptide synthesis, where it can be deprotected and combined with other amino acids to form synthetic peptides, facilitating the development of novel peptide-based therapeutics.
Used in Drug Research and Development:
In the pharmaceutical industry, (2S,4S)-4-FMoc-aMino Pyrrolidine-2-carboxylic acid Methylester-HCl is used as a crucial component in drug research and development, contributing to the discovery and optimization of new drug candidates with potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1212153-95-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,2,1,5 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1212153-95:
(9*1)+(8*2)+(7*1)+(6*2)+(5*1)+(4*5)+(3*3)+(2*9)+(1*5)=101
101 % 10 = 1
So 1212153-95-1 is a valid CAS Registry Number.
