1-(tert-Butoxycarbonyl)-4-(methoxycarbonyl)piperidine-4-carboxylic acid

95%

Reagent Code: #140833
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CAS Number 1005738-45-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 286.301 g/mol
Formula C₁₃H₂₁NO₆
badge Registry Numbers
MDL Number MFCD20923522
thermostat Physical Properties
Boiling Point 402.4±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.233±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) that require functionalized piperidine scaffolds. Its protected amine group and multiple carboxylic acid functionalities allow selective reactions in multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing peptidomimetics and CNS-targeted drugs due to the piperidine ring’s prevalence in bioactive molecules. The Boc-protected amine ensures stability during reactions, while the ester and carboxylic acid groups can be selectively hydrolyzed or coupled to other moieties, making it valuable in creating complex drug candidates.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿38,020.00
1-(tert-Butoxycarbonyl)-4-(methoxycarbonyl)piperidine-4-carboxylic acid
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) that require functionalized piperidine scaffolds. Its protected amine group and multiple carboxylic acid functionalities allow selective reactions in multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing peptidomimetics and CNS-targeted drugs due to the piperidine ring’s prevalence in bioactive molecules. The Boc-protected amine ensures stability during reactions, while the ester and carboxylic acid groups can be selectively hydrolyzed or coupled to other moieties, making it valuable in creating complex drug candidates.
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