28875-17-4 Usage
Description
BOC-L-ALANINE METHYL ESTER is a chemical compound derived from L-alanine, a naturally occurring amino acid. It is utilized in organic chemistry as a reagent for the synthesis of peptides and other organic molecules. The BOC (tert-butoxycarbonyl) group in this compound serves as a protecting group for the amino group during peptide synthesis, enabling selective reactions with other functional groups. This makes BOC-L-ALANINE METHYL ESTER a versatile and crucial building block in the creation of bioactive compounds, pharmaceuticals, and materials, with wide-ranging applications across the chemical and biotechnology industries.
Uses
Used in Organic Chemistry:
BOC-L-ALANINE METHYL ESTER is used as a reagent for the synthesis of peptides and other organic molecules, facilitating the selective reactions of functional groups in synthetic processes.
Used in Peptide Synthesis:
BOC-L-ALANINE METHYL ESTER is used as a protecting group for the amino group, ensuring that the amine functionality of the alanine molecule is safeguarded during the synthesis process, which is vital for the successful formation of peptide bonds.
Used in Pharmaceutical Production:
BOC-L-ALANINE METHYL ESTER is used as a building block in the production of bioactive compounds and pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Biotechnological Applications:
BOC-L-ALANINE METHYL ESTER is used in the biotechnology industry for the creation of materials with specific properties, such as those required for medical or industrial uses, leveraging its role in the synthesis of complex organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 28875-17-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,8,7 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 28875-17:
(7*2)+(6*8)+(5*8)+(4*7)+(3*5)+(2*1)+(1*7)=154
154 % 10 = 4
So 28875-17-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H17NO4/c1-6(7(11)13-5)10-8(12)14-9(2,3)4/h6H,1-5H3,(H,10,12)/t6-/m0/s1
28875-17-4Relevant articles and documents
Development of a temporary marker for peptides
Sameiro,Goncalves,Maia, Hernani L.S.
, p. 1480 - 1485 (2007/10/03)
3-[(N,N-Dimethylaminophenyl)-4′-diazenyl]benzoic acid was coupled with several amino acid esters and the product acylated further with Boc. The material thus obtained was then submitted to cleavage by electrolysis and nucleophilic attack in order to evaluate the possibility of using this chromophore as a temporary marker.
Synthesis of a 3-aminopiperidin-2,5-dione as a conformationally constrained surrogate of the Ala-Gly dipeptide
Estiarte, M.Angels,Diez, Anna,Rubiralta, Mario,Jackson, Richard F.W
, p. 157 - 161 (2007/10/03)
The preparation of the Boc-{Ala-Gly}-OBn pseudopeptide 4 is reported. The key intermediate, aminoester 5b, was obtained by a cross-coupling reaction of alaninezinc iodide 6 and the thioester of glycine 9.
