2-(4-Amino-1-(tert-butoxycarbonyl)piperidin-4-yl)acetic acid

≥95%

Reagent Code: #41620
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CAS Number 1159983-30-8

science Other reagents with same CAS 1159983-30-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.31 g/mol
Formula C₁₂H₂₂N₂O₄
badge Registry Numbers
MDL Number MFCD08460439
thermostat Physical Properties
Boiling Point 398.9±27.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed away from light

description Product Description

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key building block in the production of drugs targeting neurological disorders, such as Alzheimer's disease and other cognitive impairments. Additionally, it is employed in the preparation of peptide-based therapeutics, where its structure aids in enhancing stability and bioavailability. The tert-butoxycarbonyl (Boc) protecting group in the molecule is crucial for selective reactions during multi-step synthetic processes, ensuring precise modifications in the final drug compounds. Its application extends to research and development in medicinal chemistry, where it contributes to the exploration of novel drug candidates with potential therapeutic benefits.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿20,367.00
inventory 250mg
10-20 days ฿9,243.00
inventory 100mg
10-20 days ฿5,778.00

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2-(4-Amino-1-(tert-butoxycarbonyl)piperidin-4-yl)acetic acid
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This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key building block in the production of drugs targeting neurological disorders, such as Alzheimer's disease and other cognitive impairments. Additionally, it is employed in the preparation of peptide-based therapeutics, where its structure aids in enhancing stability and bioavailability. The tert-butoxycarbonyl (Boc) protecting group in the molecule is crucial for selective reactions during multi-step synthetic processes, ensuring precise modifications in the final drug compounds. Its application extends to research and development in medicinal chemistry, where it contributes to the exploration of novel drug candidates with potential therapeutic benefits.
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