tert-Butyl 3-(2-cyanopropan-2-yl)-1H-indole-1-carboxylate

98%

Reagent Code: #117391
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CAS Number 380626-46-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 284.35 g/mol
Formula C₁₇H₂₀N₂O₂
badge Registry Numbers
MDL Number MFCD02323443
thermostat Physical Properties
Boiling Point 422.1 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.06 g/cm3
Storage Room temperature, dark, inert gas

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 complex molecules, especially those containing indole structures, which are prevalent in many biologically active compounds. Its application is significant in the production of potential drug candidates, where the indole moiety plays a crucial role in binding to biological targets. Additionally, it is used in research settings to explore novel chemical reactions and pathways, aiding in the discovery of new therapeutic agents. The presence of the cyano and tert-butyl groups enhances its reactivity, making it a versatile building block in medicinal chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days €271.36
inventory 1g
10-20 days €1,244.41
inventory 250mg
10-20 days €460.98
tert-Butyl 3-(2-cyanopropan-2-yl)-1H-indole-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 complex molecules, especially those containing indole structures, which are prevalent in many biologically active compounds. Its application is significant in the production of potential drug candidates, where the indole moiety plays a crucial role in binding to biological targets. Additionally, it is used in research settings to explore novel chemical reactions and pathways, aiding in the discovery of new therapeutic agents. The presence of the cyano and tert-butyl groups enhances its reactivity, making it a versatile building block in medicinal chemistry.
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