401813-49-8 Usage
Uses
Used in Organic Synthesis:
BOC-3-(2-QUINOLYL)-DL-ALA-OH is used as a protected amine intermediate for the synthesis of complex organic molecules. The BOC group shields the amine functionality, allowing for selective reactions to occur at other sites within the molecule, which is crucial for the construction of intricate molecular architectures.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, BOC-3-(2-QUINOLYL)-DL-ALA-OH serves as a building block for the development of novel pharmaceutical agents. BOC-3-(2-QUINOLYL)-DL-ALA-OH's structural elements, including the heterocyclic 2-quinolyl group and the DL-alanine residue, can be tailored to target specific biological receptors or enzymes, potentially leading to the creation of new drugs with unique mechanisms of action.
Used in Peptide Synthesis:
BOC-3-(2-QUINOLYL)-DL-ALA-OH is utilized as a key component in the synthesis of peptides and peptidomimetics. The DL-alanine residue can be incorporated into peptide sequences, while the BOC protecting group ensures that the amine group remains unreactive until the desired point in the synthesis process, facilitating the stepwise assembly of peptide chains.
Used in Heterocyclic Chemistry:
BOC-3-(2-QUINOLYL)-DL-ALA-OH is also used as a precursor in the synthesis of heterocyclic compounds, leveraging the 2-quinolyl group's aromatic and heterocyclic characteristics. The presence of this group can influence the electronic properties of the final product, making it suitable for applications in materials science and as potential pharmaceutical agents.
Used in Research and Development:
BOC-3-(2-QUINOLYL)-DL-ALA-OH is employed in research settings to explore the chemical and biological properties of novel compounds. Its unique structure allows scientists to investigate the effects of the BOC protecting group, the 2-quinolyl moiety, and the DL-alanine residue on the compound's reactivity, stability, and potential interactions with biological targets.
Check Digit Verification of cas no
The CAS Registry Mumber 401813-49-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,1,8,1 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 401813-49:
(8*4)+(7*0)+(6*1)+(5*8)+(4*1)+(3*3)+(2*4)+(1*9)=108
108 % 10 = 8
So 401813-49-8 is a valid CAS Registry Number.
InChI:InChI=1/C17H20N2O4/c1-17(2,3)23-16(22)19-14(15(20)21)10-12-9-8-11-6-4-5-7-13(11)18-12/h4-9,14H,10H2,1-3H3,(H,19,22)(H,20,21)
401813-49-8Relevant articles and documents
Boronic ester and acid compounds, synthesis and uses
-
, (2008/06/13)
Disclosed herein are boronic ester and acid compounds, their synthesis and uses. More specifically, disclosed herein is a method for reducing the rate of degradation of proteins in an animal comprising contacting cells of the animal with certain boronic ester and acid compounds.
BORONIC ESTER AND ACID COMPOUNDS
-
, (2008/06/13)
Disclosed herein is a method for reducing the rate of degradation of proteins in an animal comprising contacting cells of the animal with certain boronic ester and acid compounds. Also disclosed herein are novel boronic ester and acid compounds, their synthesis and uses.
Intercalator amino acids: Synthesis of heteroaryl alanines
Krippner,Harding
, p. 1793 - 1804 (2007/10/02)
Stereoselective alkylation of (S)-(-)-2-t-butyl-1-t-butyloxycarbonyl-3-methyl-4-imidazolinone with 2-chloromethylquinoline, 2-chloromethylquinoxaline and 5-chloromethyl-1,10-phenanthroline, followed by hydrolysis, afforded the corresponding (S)-(+)-α-amino acids with high enantiomeric excess.
