Boc-3-(1-Pyrazolyl)-L-alanine

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Reagent Code: #151739
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CAS Number 21012-18-0

science Other reagents with same CAS 21012-18-0

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Weight 255.274 g/mol
Formula C₁₁H₁₇N₃O₄
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Storage Room temperature

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Used in peptide synthesis as a protected amino acid derivative, enabling selective incorporation of a pyrazole-functionalized alanine residue into peptide chains. The Boc group provides temporary N-terminal protection, allowing stepwise assembly under mild conditions. The pyrazolyl side chain can act as a coordinating ligand in metalloprotein mimics or serve as a hydrogen-bonding moiety in bioactive peptide design. Commonly applied in medicinal chemistry for developing enzyme inhibitors or receptor ligands where heterocyclic functionality modulates biological activity. Also useful in solid-phase synthesis due to its stability and clean deprotection profile.

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inventory 1g
10-20 days ฿30,140.00

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Boc-3-(1-Pyrazolyl)-L-alanine
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Used in peptide synthesis as a protected amino acid derivative, enabling selective incorporation of a pyrazole-functionalized alanine residue into peptide chains. The Boc group provides temporary N-terminal protection, allowing stepwise assembly under mild conditions. The pyrazolyl side chain can act as a coordinating ligand in metalloprotein mimics or serve as a hydrogen-bonding moiety in bioactive peptide design. Commonly applied in medicinal chemistry for developing enzyme inhibitors or receptor ligan

Used in peptide synthesis as a protected amino acid derivative, enabling selective incorporation of a pyrazole-functionalized alanine residue into peptide chains. The Boc group provides temporary N-terminal protection, allowing stepwise assembly under mild conditions. The pyrazolyl side chain can act as a coordinating ligand in metalloprotein mimics or serve as a hydrogen-bonding moiety in bioactive peptide design. Commonly applied in medicinal chemistry for developing enzyme inhibitors or receptor ligands where heterocyclic functionality modulates biological activity. Also useful in solid-phase synthesis due to its stability and clean deprotection profile.

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