2-((1H-Indol-3-yl)methylene)malononitrile

98%

Reagent Code: #41111
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CAS Number 75629-62-8

science Other reagents with same CAS 75629-62-8

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Weight 193.2041 g/mol
Formula C₁₂H₇N₃
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MDL Number MFCD00022740
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This compound is primarily utilized in organic synthesis and material science due to its unique chemical structure. It serves as a key intermediate in the production of various heterocyclic compounds, which are essential in the development of pharmaceuticals and agrochemicals. Its ability to act as a precursor in the synthesis of indole derivatives makes it valuable in drug discovery, particularly for compounds with potential anticancer, antiviral, and anti-inflammatory properties. Additionally, it is employed in the fabrication of organic electronic materials, where its conjugated system contributes to the development of optoelectronic devices such as organic light-emitting diodes (OLEDs) and sensors. Its reactivity with various nucleophiles also makes it useful in the creation of novel polymers and dyes.

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inventory 100mg
10-20 days ฿1,008.00

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2-((1H-Indol-3-yl)methylene)malononitrile
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This compound is primarily utilized in organic synthesis and material science due to its unique chemical structure. It serves as a key intermediate in the production of various heterocyclic compounds, which are essential in the development of pharmaceuticals and agrochemicals. Its ability to act as a precursor in the synthesis of indole derivatives makes it valuable in drug discovery, particularly for compounds with potential anticancer, antiviral, and anti-inflammatory properties. Additionally, it is em

This compound is primarily utilized in organic synthesis and material science due to its unique chemical structure. It serves as a key intermediate in the production of various heterocyclic compounds, which are essential in the development of pharmaceuticals and agrochemicals. Its ability to act as a precursor in the synthesis of indole derivatives makes it valuable in drug discovery, particularly for compounds with potential anticancer, antiviral, and anti-inflammatory properties. Additionally, it is employed in the fabrication of organic electronic materials, where its conjugated system contributes to the development of optoelectronic devices such as organic light-emitting diodes (OLEDs) and sensors. Its reactivity with various nucleophiles also makes it useful in the creation of novel polymers and dyes.

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