(S)-3-((tert-Butoxycarbonyl)amino)-3-(6-methoxypyridin-3-yl)propanoic acid

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Reagent Code: #38387
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CAS Number 1217755-81-1

science Other reagents with same CAS 1217755-81-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 296.3190 g/mol
Formula C₁₄H₂₀N₂O₅
badge Registry Numbers
MDL Number MFCD04118073
inventory_2 Storage & Handling
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description Product Description

This compound is primarily used in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a methoxypyridine moiety, makes it a valuable intermediate in organic synthesis. The Boc group is often employed to protect amines during multi-step reactions, ensuring selective transformations. The methoxypyridine component can contribute to the biological activity of the final drug molecule, potentially enhancing binding affinity or modulating pharmacokinetic properties. It is commonly utilized in the preparation of compounds targeting neurological disorders, inflammation, or other therapeutic areas where pyridine derivatives play a role. Additionally, its chiral center allows for the creation of enantiomerically pure drugs, which is critical for ensuring efficacy and reducing side effects.

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inventory 100mg
10-20 days ฿14,940.00

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(S)-3-((tert-Butoxycarbonyl)amino)-3-(6-methoxypyridin-3-yl)propanoic acid
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This compound is primarily used in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a methoxypyridine moiety, makes it a valuable intermediate in organic synthesis. The Boc group is often employed to protect amines during multi-step reactions, ensuring selective transformations. The methoxypyridine component can contribute to the biological activity of the final drug mol

This compound is primarily used in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a methoxypyridine moiety, makes it a valuable intermediate in organic synthesis. The Boc group is often employed to protect amines during multi-step reactions, ensuring selective transformations. The methoxypyridine component can contribute to the biological activity of the final drug molecule, potentially enhancing binding affinity or modulating pharmacokinetic properties. It is commonly utilized in the preparation of compounds targeting neurological disorders, inflammation, or other therapeutic areas where pyridine derivatives play a role. Additionally, its chiral center allows for the creation of enantiomerically pure drugs, which is critical for ensuring efficacy and reducing side effects.

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