(R)-2-(1-(tert-Butoxycarbonyl)piperidin-2-yl)acetic acid

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Reagent Code: #37469
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CAS Number 351410-32-7

science Other reagents with same CAS 351410-32-7

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Weight 243.2900 g/mol
Formula C₁₂H₂₁NO₄
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MDL Number MFCD06656438
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description Product Description

This chemical is primarily utilized in the pharmaceutical and organic synthesis industries. It serves as a key intermediate in the production of various bioactive compounds, particularly those targeting neurological and cardiovascular diseases. Its structure, featuring a piperidine ring and a tert-butoxycarbonyl (Boc) protecting group, makes it valuable for constructing complex molecules with high precision. The Boc group can be easily removed under mild acidic conditions, allowing for further functionalization. Additionally, it is employed in the development of peptide-based drugs and enzyme inhibitors, where its chiral center ensures the desired stereochemistry in the final product. Its application extends to research settings for studying receptor interactions and drug delivery mechanisms.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿880.00

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(R)-2-(1-(tert-Butoxycarbonyl)piperidin-2-yl)acetic acid
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This chemical is primarily utilized in the pharmaceutical and organic synthesis industries. It serves as a key intermediate in the production of various bioactive compounds, particularly those targeting neurological and cardiovascular diseases. Its structure, featuring a piperidine ring and a tert-butoxycarbonyl (Boc) protecting group, makes it valuable for constructing complex molecules with high precision. The Boc group can be easily removed under mild acidic conditions, allowing for further functional

This chemical is primarily utilized in the pharmaceutical and organic synthesis industries. It serves as a key intermediate in the production of various bioactive compounds, particularly those targeting neurological and cardiovascular diseases. Its structure, featuring a piperidine ring and a tert-butoxycarbonyl (Boc) protecting group, makes it valuable for constructing complex molecules with high precision. The Boc group can be easily removed under mild acidic conditions, allowing for further functionalization. Additionally, it is employed in the development of peptide-based drugs and enzyme inhibitors, where its chiral center ensures the desired stereochemistry in the final product. Its application extends to research settings for studying receptor interactions and drug delivery mechanisms.

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