(S)-2-(tert-Butoxycarbonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid

95%

Reagent Code: #38166
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CAS Number 151004-94-3

science Other reagents with same CAS 151004-94-3

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Weight 277.3157 g/mol
Formula C₁₅H₁₉NO₄
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MDL Number MFCD15474917
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of peptidomimetics and bioactive molecules. It serves as a key intermediate in the production of compounds that mimic peptide structures, which are essential in drug discovery for targeting specific biological pathways. Its tert-butoxycarbonyl (Boc) protecting group is crucial in peptide synthesis, as it safeguards the amine functionality during reactions, allowing for selective deprotection and further modification. Additionally, it is employed in the preparation of tetrahydroisoquinoline derivatives, which are known for their potential therapeutic applications, including antimicrobial, anticancer, and central nervous system activities. Its role in organic synthesis highlights its importance in creating complex molecules for medicinal chemistry and research.

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inventory 100mg
10-20 days ฿13,428.00

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(S)-2-(tert-Butoxycarbonyl)-1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid
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This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of peptidomimetics and bioactive molecules. It serves as a key intermediate in the production of compounds that mimic peptide structures, which are essential in drug discovery for targeting specific biological pathways. Its tert-butoxycarbonyl (Boc) protecting group is crucial in peptide synthesis, as it safeguards the amine functionality during reactions, allowing for selective deprotection and furth

This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of peptidomimetics and bioactive molecules. It serves as a key intermediate in the production of compounds that mimic peptide structures, which are essential in drug discovery for targeting specific biological pathways. Its tert-butoxycarbonyl (Boc) protecting group is crucial in peptide synthesis, as it safeguards the amine functionality during reactions, allowing for selective deprotection and further modification. Additionally, it is employed in the preparation of tetrahydroisoquinoline derivatives, which are known for their potential therapeutic applications, including antimicrobial, anticancer, and central nervous system activities. Its role in organic synthesis highlights its importance in creating complex molecules for medicinal chemistry and research.

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