63769-98-2 Usage
Description
BOC-ALA-ALA-PRO-OH, also known as N-tert-Butoxycarbonyl Alanine Alanine Proline, is a chemical compound that serves as a building block in peptide synthesis. It is a protected form of the amino acid proline, featuring a tert-butyloxycarbonyl group attached to the amino group. This protection allows for selective deprotection and coupling with other amino acids during the synthesis process, making it a valuable component in the creation of pharmaceuticals, agrochemicals, and materials science applications where precise peptide chain formation is crucial.
Uses
Used in Pharmaceutical Industry:
BOC-ALA-ALA-PRO-OH is used as a key building block for the synthesis of peptides and proteins. Its role in this industry is crucial for the development of new drugs and therapeutic agents, as it allows for the controlled assembly of complex peptide structures.
Used in Agrochemical Industry:
In the agrochemical sector, BOC-ALA-ALA-PRO-OH is utilized as a component in the synthesis of bioactive peptides. These peptides can have applications in pest control, plant protection, and other agricultural areas, contributing to more effective and targeted agrochemical products.
Used in Materials Science:
BOC-ALA-ALA-PRO-OH is employed in materials science for the development of advanced materials with specific properties. The controlled synthesis of peptides using this compound can lead to the creation of biomaterials, sensors, and other innovative materials with applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 63769-98-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,7,6 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 63769-98:
(7*6)+(6*3)+(5*7)+(4*6)+(3*9)+(2*9)+(1*8)=172
172 % 10 = 2
So 63769-98-2 is a valid CAS Registry Number.
63769-98-2Relevant articles and documents
Design of a novel secondary structure scaffolding device: Induction of a reverse turn in tetrapeptides by incorporating a β-amino acid and stereocontrolled free radical α-substitution reactions in peptide motifs
Hanessian, Stephen,Yang, Hua
, p. 3155 - 3158 (2007/10/03)
The incorporation of α-substituted β-amino acids into a tetrapeptide motif induces a reverse rum in aprotic solvent systems as revealed by NOESY and ROESY techniques, and by CD spectra. The conformations of these compounds have been studied by molecular modeling, and further supported by performing a highly stereoselective free radical allylation reaction on an α-phenylseleno β-amino acid unit within the tetrapeptide.
NEW SYNTHESIS OF PEPTIDE SUBSTRATES AND INHIBITORS OF HUMAN GRANULOCYTE ELASTASE
Martynov, V. F.,Leont'eva, L. I.,Sorochinskaya, E. I.,Smirnov, A. O.
, p. 384 - 388 (2007/10/02)
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