tert-butyl 2-amino-3-cyano-5-fluoro-1H-indol-7-yl(methyl)carbamate

Reagent Code: #54610
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CAS Number 1400808-30-1

science Other reagents with same CAS 1400808-30-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 304.32 g/mol
Formula C₁₅H₁₇FN₄O₂
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This chemical is primarily utilized in the pharmaceutical and organic synthesis fields. It serves as a key intermediate in the development of biologically active compounds, particularly in the synthesis of novel indole-based molecules. These molecules are often explored for their potential therapeutic properties, including anticancer, antiviral, and anti-inflammatory activities. The presence of the fluoro and cyano groups enhances its reactivity and selectivity, making it valuable in the construction of complex drug candidates. Additionally, its tert-butyl carbamate moiety provides stability and protection during multi-step synthetic processes, facilitating efficient chemical transformations.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿9,000.00

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tert-butyl 2-amino-3-cyano-5-fluoro-1H-indol-7-yl(methyl)carbamate
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This chemical is primarily utilized in the pharmaceutical and organic synthesis fields. It serves as a key intermediate in the development of biologically active compounds, particularly in the synthesis of novel indole-based molecules. These molecules are often explored for their potential therapeutic properties, including anticancer, antiviral, and anti-inflammatory activities. The presence of the fluoro and cyano groups enhances its reactivity and selectivity, making it valuable in the construction of

This chemical is primarily utilized in the pharmaceutical and organic synthesis fields. It serves as a key intermediate in the development of biologically active compounds, particularly in the synthesis of novel indole-based molecules. These molecules are often explored for their potential therapeutic properties, including anticancer, antiviral, and anti-inflammatory activities. The presence of the fluoro and cyano groups enhances its reactivity and selectivity, making it valuable in the construction of complex drug candidates. Additionally, its tert-butyl carbamate moiety provides stability and protection during multi-step synthetic processes, facilitating efficient chemical transformations.

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