(R,S)-2-Isobutyl-3-(boc-amino)propanoic acid

95%

Reagent Code: #37792
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CAS Number 828254-17-7

science Other reagents with same CAS 828254-17-7

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Weight 245.3153 g/mol
Formula C₁₂H₂₃NO₄
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MDL Number MFCD11973912
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description Product Description

This compound is primarily used in the synthesis of peptides and pharmaceutical intermediates. It serves as a protected amino acid derivative, where the Boc (tert-butoxycarbonyl) group safeguards the amine functionality during chemical reactions. This protection is crucial in multi-step organic synthesis, particularly in the production of complex molecules like peptides, where selective reactivity is required. Additionally, it is employed in the development of bioactive compounds and drug candidates, especially in medicinal chemistry research. Its role in facilitating the controlled assembly of amino acids makes it valuable for creating peptide-based therapeutics and studying structure-activity relationships.

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inventory 100mg
10-20 days ฿6,813.00

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(R,S)-2-Isobutyl-3-(boc-amino)propanoic acid
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This compound is primarily used in the synthesis of peptides and pharmaceutical intermediates. It serves as a protected amino acid derivative, where the Boc (tert-butoxycarbonyl) group safeguards the amine functionality during chemical reactions. This protection is crucial in multi-step organic synthesis, particularly in the production of complex molecules like peptides, where selective reactivity is required. Additionally, it is employed in the development of bioactive compounds and drug candidates, esp

This compound is primarily used in the synthesis of peptides and pharmaceutical intermediates. It serves as a protected amino acid derivative, where the Boc (tert-butoxycarbonyl) group safeguards the amine functionality during chemical reactions. This protection is crucial in multi-step organic synthesis, particularly in the production of complex molecules like peptides, where selective reactivity is required. Additionally, it is employed in the development of bioactive compounds and drug candidates, especially in medicinal chemistry research. Its role in facilitating the controlled assembly of amino acids makes it valuable for creating peptide-based therapeutics and studying structure-activity relationships.

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