37535-57-2 Usage
Description
(S)-N-Boc-(4-Pyridyl)alanine, also known as Boc-3-(4-pyridyl)-L-alanine, is a protected form of L-Alanine, a non-essential amino acid naturally found in the human body and obtained through our diet. It is characterized by its off-white to light yellow powder appearance and is used in various applications across different industries due to its unique chemical properties.
Uses
Used in Pharmaceutical Industry:
(S)-N-Boc-(4-Pyridyl)alanine is used as an intermediate in the synthesis of various pharmaceutical compounds for [application reason]. Its unique structure allows for the development of new drugs with potential therapeutic benefits.
Used in Chemical Research:
In the field of chemical research, (S)-N-Boc-(4-Pyridyl)alanine is used as a research compound for [application reason]. Its properties make it a valuable tool for understanding the behavior of amino acids and their derivatives in various chemical reactions and processes.
Used in Peptide Synthesis:
(S)-N-Boc-(4-Pyridyl)alanine is used as a building block in the synthesis of peptides for [application reason]. Its protected form allows for the controlled formation of peptide bonds, which is crucial in the development of peptide-based drugs and therapeutics.
Used in Material Science:
In material science, (S)-N-Boc-(4-Pyridyl)alanine is used as a component in the development of novel materials for [application reason]. Its unique chemical properties can contribute to the creation of advanced materials with specific characteristics and applications.
Used in Analytical Chemistry:
(S)-N-Boc-(4-Pyridyl)alanine is used as a reference compound in analytical chemistry for [application reason]. Its distinct properties make it suitable for calibration and quality control in various analytical techniques and methods.
Check Digit Verification of cas no
The CAS Registry Mumber 37535-57-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,5,3 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 37535-57:
(7*3)+(6*7)+(5*5)+(4*3)+(3*5)+(2*5)+(1*7)=132
132 % 10 = 2
So 37535-57-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H18N2O4/c1-13(2,3)19-12(18)15-10(11(16)17)8-9-4-6-14-7-5-9/h4-7,10H,8H2,1-3H3,(H,15,18)(H,16,17)/t10-/m0/s1
37535-57-2Relevant articles and documents
EPOXYKETONE COMPOUNDS FOR ENZYME INHIBITION
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Paragraph 00117; 00118, (2016/02/26)
The present disclosure relates to novel compounds and pharmaceutical compositions thereof which are useful as inhibitors of proteasomes. The compounds provided herein have improved proteasome potency and selectivity, and increased aqueous solubility, and
Studies on polypeptides XXXII. Solid-phase synthesis of RNase S-peptide 1-14 analogues; replacement of histidine-12 by β-(2-pyridyl)-L-alanine and β-(4-pyridyl)-L-alanine
Hoes, C.,Raap, J.,Bloemhoff, W.,Kerling, K. E. T.
, p. 99 - 104 (2007/10/02)
The synthesis of two analogues of the N-terminal tetradecapeptide of ribonuclease A (RNase S-peptide 1-14), in which the active site histidine-12 residue is replaced by β-(2-pyridyl)-L-alanine and β-(4-pyridyl)-L-alanine, has been accomplished by the solid-phase method.The enantiomers of β-(2-pyridyl)alanine were obtained by chymotryptic hydrolysis of its racemic Nα-acetyl ethyl ester.The Boc derivative of both L-amino acids has been synthesized.
