133565-42-1 Usage
Description
BOC-L-GLUTAMINOL, also known as Boc-Gln-OH, is a chemical compound that serves as an amino acid derivative with a Boc-protected glutamine residue. It is a fundamental building block in the synthesis of peptides and proteins, playing a crucial role in organic chemistry for the development of new molecules and compounds.
Uses
Used in Organic Synthesis:
BOC-L-GLUTAMINOL is used as a reagent for introducing glutamine residues into peptide chains, particularly in solid-phase peptide synthesis. Its Boc-protected structure ensures stable handling and compatibility with various solvents and reagents, facilitating the synthesis of complex peptide structures.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, BOC-L-GLUTAMINOL is utilized as a key intermediate in the synthesis of various drugs. Its ability to incorporate glutamine residues into drug molecules contributes to the development of bioactive compounds with potential therapeutic applications.
Used in Agrochemical Synthesis:
BOC-L-GLUTAMINOL also finds application in the agrochemical sector, where it is employed in the synthesis of bioactive compounds for agricultural use. Its role in creating specific molecular structures aids in the development of effective agrochemicals for crop protection and enhancement.
Overall, BOC-L-GLUTAMINOL is a versatile chemical tool across different industries, including organic synthesis, pharmaceuticals, and agrochemicals, due to its unique properties and reactivity in introducing glutamine residues into various molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 133565-42-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,5,6 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 133565-42:
(8*1)+(7*3)+(6*3)+(5*5)+(4*6)+(3*5)+(2*4)+(1*2)=121
121 % 10 = 1
So 133565-42-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H20N2O4/c1-10(2,3)16-9(15)12-7(6-13)4-5-8(11)14/h7,13H,4-6H2,1-3H3,(H2,11,14)(H,12,15)/t7-/m0/s1
133565-42-1Relevant articles and documents
STAT DEGRADERS AND USES THEREOF
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, (2021/09/26)
The present invention provides compounds, compositions thereof, and methods of using the same.
A facile synthesis of chiral N-protected β-amino alcohols
Rodriguez,Llinares,Doulut,Heitz,Martinez
, p. 923 - 926 (2007/10/02)
Chiral N-protected β-amino alcohols are easily obtained by NaBH4 reduction of mixed anhydrides of N-protected α-amino acids in an organic/aqueous medium. The alcohols obtained from side chain or main chain reduction of N-protected aspartic acid are converted in good yields into lactones.
