(R)-tert-Butyl (piperidin-3-ylmethyl)carbamate

97%

Reagent Code: #113606
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CAS Number 879275-33-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.31 g/mol
Formula C₁₁H₂₂N₂O₂
badge Registry Numbers
MDL Number MFCD03093384
thermostat Physical Properties
Boiling Point 321.8±15.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed away from light

description Product Description

This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various biologically active compounds. Its structure, featuring a piperidine ring and a carbamate group, makes it valuable for the development of drugs targeting the central nervous system. It is often employed in the creation of inhibitors for enzymes or receptors involved in neurological disorders, such as Alzheimer's disease or schizophrenia. Additionally, its chiral nature allows for the production of enantiomerically pure compounds, enhancing the specificity and efficacy of the resulting pharmaceuticals. Researchers also use it in the design of prodrugs, where its tert-butyl group can be cleaved under specific conditions to release the active drug molecule.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to Yellow Solid
Purity (%) 96.5-100%
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 10g
10-20 days ฿15,880.00
inventory 1g
10-20 days ฿2,260.00
inventory 5g
10-20 days ฿8,660.00
(R)-tert-Butyl (piperidin-3-ylmethyl)carbamate
This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various biologically active compounds. Its structure, featuring a piperidine ring and a carbamate group, makes it valuable for the development of drugs targeting the central nervous system. It is often employed in the creation of inhibitors for enzymes or receptors involved in neurological disorders, such as Alzheimer's disease or schizophrenia. Additionally, its chiral nature allows for the production of enantiomerically pure compounds, enhancing the specificity and efficacy of the resulting pharmaceuticals. Researchers also use it in the design of prodrugs, where its tert-butyl group can be cleaved under specific conditions to release the active drug molecule.
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