58171-88-3 Usage
Uses
Used in Pharmaceutical Research and Development:
Z-BETA-ALA-GLY-OH is used as a chemical building block for the synthesis of pharmaceutical drugs and biologically active compounds. Its incorporation into peptide and protein structures allows for the development of new therapeutic agents with potential applications in various medical fields.
Used in Biochemistry Research:
In the field of biochemistry, Z-BETA-ALA-GLY-OH is used as a research tool to study the properties and interactions of amino acids and peptides. Its ability to form complex peptide structures aids in understanding the fundamental processes of protein synthesis and function.
Used in Organic Chemistry:
Z-BETA-ALA-GLY-OH is employed in organic chemistry as a versatile intermediate for the synthesis of a wide range of organic compounds. Its reactivity and functional groups enable the formation of various chemical bonds and the creation of diverse molecular structures.
Used in Peptide Synthesis:
Z-BETA-ALA-GLY-OH is used as a key component in the synthesis of peptides, providing a stable and protected building block for the assembly of larger peptide chains. Its presence in peptide synthesis allows for the controlled formation of peptide bonds and the production of well-defined peptide sequences.
Overall, Z-BETA-ALA-GLY-OH is a multifaceted chemical compound with applications across various scientific disciplines, including pharmaceutical research, biochemistry, organic chemistry, and peptide synthesis. Its versatility and utility as a building block make it an indispensable tool in the development of new drugs, therapeutic agents, and biologically active compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 58171-88-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,1,7 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 58171-88:
(7*5)+(6*8)+(5*1)+(4*7)+(3*1)+(2*8)+(1*8)=143
143 % 10 = 3
So 58171-88-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H16N2O5/c16-11(15-8-12(17)18)6-7-14-13(19)20-9-10-4-2-1-3-5-10/h1-5H,6-9H2,(H,14,19)(H,15,16)(H,17,18)
58171-88-3Relevant academic research and scientific papers
Tandem deprotection-dimerization-macrocyclization route to C2 symmetric cyclo-tetrapeptides
Ha, Khanh,Lebedyeva, Iryna,Hamedzadeh, Sadra,Li, Zhiliang,Quinones, Ryan,Pillai, Girinath G.,Williams, Byron,Nasajpour, Amir,Martin, Kristin,Asiri, Abdullah M.,Katritzky, Alan R.
, p. 4874 - 4879 (2014/05/06)
Dimerization-macrocyclization has been a long-standing problem in the cyclization of peptides since, together with the desired cyclic product, many cyclic oligomers and linear polymers may also be formed during the reaction. Therefore, the development of a process that affords the cyclic dimer predominantly is difficult. A novel and versatile strategy for the synthesis of symmetric cyclo-tetrapeptides by palladium-promoted tandem deprotection/cyclo- dimerization from readily available Cbz-dipeptidoyl benzotriazolides is reported (Cbz=carboxybenzyl).
