(3R,4R)-Rel-1-[(tert-butoxy)carbonyl]-4-methylpiperidine-3-carboxylic acid

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Reagent Code: #36749
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CAS Number 1469287-58-8

science Other reagents with same CAS 1469287-58-8

blur_circular Chemical Specifications

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Weight 243.30 g/mol
Formula C₁₂H₂₁NO₄
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description Product Description

This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). Its structure makes it a valuable intermediate in the production of complex molecules, especially those targeting neurological and cardiovascular diseases. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactions during synthesis, enhancing the efficiency of multi-step processes. Additionally, its chiral centers are crucial for creating enantiomerically pure drugs, which are essential for optimizing therapeutic efficacy and minimizing side effects. It is also employed in research settings for studying enzyme interactions and receptor binding due to its specific stereochemistry.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿67,464.00
inventory 100mg
10-20 days ฿15,210.00
inventory 250mg
10-20 days ฿25,362.00

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(3R,4R)-Rel-1-[(tert-butoxy)carbonyl]-4-methylpiperidine-3-carboxylic acid
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This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). Its structure makes it a valuable intermediate in the production of complex molecules, especially those targeting neurological and cardiovascular diseases. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactions during synthesis, enhancing the efficiency of multi-step processes. Additionally, its chiral centers are crucial for creating en

This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). Its structure makes it a valuable intermediate in the production of complex molecules, especially those targeting neurological and cardiovascular diseases. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactions during synthesis, enhancing the efficiency of multi-step processes. Additionally, its chiral centers are crucial for creating enantiomerically pure drugs, which are essential for optimizing therapeutic efficacy and minimizing side effects. It is also employed in research settings for studying enzyme interactions and receptor binding due to its specific stereochemistry.

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