tert-butyl 4-((2-bromophenyl)amino)-4-cyanopiperidine-1-carboxylate

95%

Reagent Code: #83756
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CAS Number 205813-91-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 380.28 g/mol
Formula C₁₇H₂₂BrN₃O₂
badge Registry Numbers
MDL Number MFCD31706248
thermostat Physical Properties
Boiling Point 503.0±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.37±0.1 g/cm3(Predicted)
Storage room temperature

description Product Description

This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a key intermediate in the synthesis of various biologically active molecules, including potential drug candidates. Its structure, featuring a piperidine ring, a cyano group, and a bromophenyl moiety, makes it valuable for constructing complex molecules with specific pharmacological properties. Researchers often employ it in the design and optimization of compounds targeting neurological disorders, cancer, or infectious diseases. Additionally, its reactive sites allow for further functionalization, enabling the creation of diverse chemical libraries for drug discovery and development.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,360.00
inventory 250mg
10-20 days ฿17,550.00
inventory 1g
10-20 days ฿35,100.00
tert-butyl 4-((2-bromophenyl)amino)-4-cyanopiperidine-1-carboxylate
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a key intermediate in the synthesis of various biologically active molecules, including potential drug candidates. Its structure, featuring a piperidine ring, a cyano group, and a bromophenyl moiety, makes it valuable for constructing complex molecules with specific pharmacological properties. Researchers often employ it in the design and optimization of compounds targeting neurological disorders, cancer, or infectious diseases. Additionally, its reactive sites allow for further functionalization, enabling the creation of diverse chemical libraries for drug discovery and development.
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