4-((1-(Tert-butoxycarbonyl)piperidin-4-yl)methyl)benzoicacid

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Reagent Code: #244366
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CAS Number 147969-86-6

science Other reagents with same CAS 147969-86-6

blur_circular Chemical Specifications

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Weight 319.4 g/mol
Formula C₁₈H₂₅NO₄
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its carboxylic acid group allows for easy coupling with amines to form amide bonds, making it valuable in constructing complex drug-like structures. The Boc-protected piperidine moiety provides a handle for further functionalization while maintaining stability during reactions. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its favorable solubility and steric properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,810.00
inventory 250mg
10-20 days ฿13,010.00
inventory 1g
10-20 days ฿39,890.00

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4-((1-(Tert-butoxycarbonyl)piperidin-4-yl)methyl)benzoicacid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its carboxylic acid group allows for easy coupling with amines to form amide bonds, making it valuable in constructing complex drug-like structures. The Boc-protected piperidine moiety provides a handle for further functionalization while maintaining stability during reactions. Commonly employed in medicinal chemistry for structure-activity relations

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its carboxylic acid group allows for easy coupling with amines to form amide bonds, making it valuable in constructing complex drug-like structures. The Boc-protected piperidine moiety provides a handle for further functionalization while maintaining stability during reactions. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its favorable solubility and steric properties.

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