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3-(5-Methoxypyridin-2-yl)-N-BOC-DL-alanine is a chemical compound with the molecular formula C15H21N3O5. It is a derivative of alanine, an essential α-amino acid involved in protein biosynthesis. 3-(5-METHOXYPYRIDIN-2-YL)-N-BOC-DL-ALANINE features a BOC (tert-butyloxycarbonyl) protecting group, which is crucial for its application in peptide synthesis and as a building block for pharmaceutical compounds. The 3-(5-methoxypyridin-2-yl) group, a heterocyclic aromatic ring, endows the molecule with unique properties, making it a valuable component in medicinal chemistry and drug development. Its potential as a selective ligand for specific receptors or enzymes, along with the solubility and bioavailability benefits provided by the methoxy substituent, positions 3-(5-METHOXYPYRIDIN-2-YL)-N-BOC-DL-ALANINE as a promising candidate for various pharmaceutical applications.

209526-94-3

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209526-94-3 Usage

Uses

Used in Pharmaceutical Industry:
3-(5-Methoxypyridin-2-yl)-N-BOC-DL-alanine is used as a building block for the development of pharmaceutical compounds due to its ability to serve as a selective ligand for certain receptors or enzymes. Its unique structural features and the presence of the BOC protecting group make it suitable for peptide synthesis, contributing to the creation of novel drug candidates with potential therapeutic applications.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 3-(5-Methoxypyridin-2-yl)-N-BOC-DL-alanine is utilized as a key component in the design and synthesis of new molecules with potential biological activities. Its heterocyclic aromatic ring and methoxy substituent can be exploited to modulate the physicochemical properties of drug candidates, enhancing their solubility, bioavailability, and overall pharmacokinetic profile.
Used in Drug Synthesis and Peptide Assembly:
3-(5-Methoxypyridin-2-yl)-N-BOC-DL-alanine is employed as a protected amino acid in the synthesis of peptides and other biomolecules. The BOC protecting group ensures that the amino acid's side chain remains unreactive during the assembly process, allowing for the controlled formation of peptide bonds and the synthesis of complex peptide structures with desired biological functions.

Check Digit Verification of cas no

The CAS Registry Mumber 209526-94-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,9,5,2 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 209526-94:
(8*2)+(7*0)+(6*9)+(5*5)+(4*2)+(3*6)+(2*9)+(1*4)=143
143 % 10 = 3
So 209526-94-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H20N2O5/c1-14(2,3)21-13(19)16-11(12(17)18)7-9-5-6-10(20-4)8-15-9/h5-6,8,11H,7H2,1-4H3,(H,16,19)(H,17,18)

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