2-(6-Bromo-1H-Indol-3-Yl)Acetonitrile

97%

Reagent Code: #154226
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CAS Number 152213-61-1

science Other reagents with same CAS 152213-61-1

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Weight 235.08 g/mol
Formula C₁₀H₇BrN₂
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Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of serotonin receptor modulators and anti-migraine agents. It plays an important role in constructing indole-based scaffolds found in biologically active molecules. Commonly employed in research settings for the preparation of tryptamine and tryptophan derivatives. Also utilized in the production of agrochemicals and in the study of kinase inhibitors due to its ability to participate in cyclization and substitution reactions. Its nitrile and bromo functional groups allow for diverse chemical transformations, making it valuable in medicinal chemistry and drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,700.00
inventory 250mg
10-20 days ฿6,290.00
inventory 1g
10-20 days ฿16,960.00
inventory 5g
10-20 days ฿62,490.00

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2-(6-Bromo-1H-Indol-3-Yl)Acetonitrile
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of serotonin receptor modulators and anti-migraine agents. It plays an important role in constructing indole-based scaffolds found in biologically active molecules. Commonly employed in research settings for the preparation of tryptamine and tryptophan derivatives. Also utilized in the production of agrochemicals and in the study of kinase inhibitors due to its ability to participate in cyclization and substit

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of serotonin receptor modulators and anti-migraine agents. It plays an important role in constructing indole-based scaffolds found in biologically active molecules. Commonly employed in research settings for the preparation of tryptamine and tryptophan derivatives. Also utilized in the production of agrochemicals and in the study of kinase inhibitors due to its ability to participate in cyclization and substitution reactions. Its nitrile and bromo functional groups allow for diverse chemical transformations, making it valuable in medicinal chemistry and drug discovery.

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