136315-71-4 Usage
Description
Boc-trans-2-amino cyclopentane carboxylic acid is a versatile chemical compound featuring a cyclopentane ring with an amino group and a carboxylic acid group. The "Boc" prefix indicates the presence of a tert-butoxycarbonyl protecting group, which shields the amino group from unwanted reactions during organic synthesis. Boc-trans-2-aMinocyclopentane
carboxylic acid serves as a crucial intermediate in the creation of various pharmaceuticals and biologically active molecules, playing a significant role in peptide synthesis and as a building block in organic chemistry.
Uses
Used in Pharmaceutical Synthesis:
Boc-trans-2-amino cyclopentane carboxylic acid is utilized as a key intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs with potential therapeutic applications. Its unique structure and reactivity allow for the creation of diverse molecular entities with specific biological activities.
Used in Peptide Synthesis:
In the field of peptide synthesis, Boc-trans-2-amino cyclopentane carboxylic acid acts as a building block, facilitating the assembly of peptide sequences with desired properties. The Boc protecting group ensures that the amino group remains intact and unreactive until the desired point in the synthesis process, allowing for precise control over the formation of peptide bonds.
Used in Organic Chemistry:
Boc-trans-2-amino cyclopentane carboxylic acid is also employed as a versatile compound in organic chemistry, enabling the synthesis of a wide range of organic molecules. Its unique structure allows for various chemical reactions, making it a valuable component in the construction of complex organic compounds.
Used in Drug Discovery:
In the realm of drug discovery, Boc-trans-2-amino cyclopentane carboxylic acid plays a significant role as a precursor to biologically active molecules. Its ability to be incorporated into diverse chemical structures makes it a promising candidate for the development of new therapeutic agents with novel mechanisms of action.
Used in Chemical Research:
Boc-trans-2-amino cyclopentane carboxylic acid is also valuable in chemical research, where it can be used to explore new reaction pathways, investigate the properties of cyclopentane rings, and study the effects of protecting groups on amino acid reactivity. This research can lead to advancements in synthetic methodologies and a deeper understanding of organic chemistry principles.
Check Digit Verification of cas no
The CAS Registry Mumber 136315-71-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,3,1 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 136315-71:
(8*1)+(7*3)+(6*6)+(5*3)+(4*1)+(3*5)+(2*7)+(1*1)=114
114 % 10 = 4
So 136315-71-4 is a valid CAS Registry Number.
136315-71-4Relevant articles and documents
Radical cyclization in heterocycle synthesis. Part 13: Sulfanyl radical addition-cyclization of oxime ethers and hydrazones connected with alkenes for synthesis of cyclic β-amino acids
Miyata, Okiko,Muroya, Kanami,Kobayashi, Tomoko,Yamanaka, Rina,Kajisa, Seiko,Koide, Junko,Naito, Takeaki
, p. 4459 - 4479 (2007/10/03)
A combination of sulfanyl radical addition-cyclization of the oxime ethers and hydrazones connected with alkenes and subsequent conversion of a phenylsulfanylmethyl group to a carboxyl group provides a novel method for the construction of the cyclic β-amino acids. Upon treatment with thiophenol in the presence of AIBN, the oxime ethers and hydrazones smoothly underwent sulfanyl radical addition-cyclization to give the 2-(phenylsulfanylmethyl)cycloalkylamine. This method was successfully applied to the practical synthesis of 2-aminocyclopentanecarboxylic acid and 4-amino-3-pyrrolidinecarboxylic acid.
