2-Phenyl-1H-indol-5-amine

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Reagent Code: #225430
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CAS Number 6855-64-7

science Other reagents with same CAS 6855-64-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 208.26 g/mol
Formula C₁₄H₁₂N₂
badge Registry Numbers
MDL Number MFCD17012057
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of serotonin receptor modulators. It serves as a building block for compounds with potential neuroactive properties. Commonly employed in research settings for the preparation of indole-based bioactive molecules. Also utilized in the creation of dyes and fluorescent probes due to its conjugated aromatic structure. Shows relevance in medicinal chemistry for designing analogs with anti-inflammatory and anticancer activities. Additionally, used as a reagent in studying carbon-carbon bond formation in organic reactions.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿2,040.00
inventory 250mg
10-20 days ฿6,150.00

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2-Phenyl-1H-indol-5-amine
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of serotonin receptor modulators. It serves as a building block for compounds with potential neuroactive properties. Commonly employed in research settings for the preparation of indole-based bioactive molecules. Also utilized in the creation of dyes and fluorescent probes due to its conjugated aromatic structure. Shows relevance in medicinal chemistry for designing analogs with anti-inflammatory and anticancer activit

Used in the synthesis of pharmaceutical intermediates, particularly in the development of serotonin receptor modulators. It serves as a building block for compounds with potential neuroactive properties. Commonly employed in research settings for the preparation of indole-based bioactive molecules. Also utilized in the creation of dyes and fluorescent probes due to its conjugated aromatic structure. Shows relevance in medicinal chemistry for designing analogs with anti-inflammatory and anticancer activities. Additionally, used as a reagent in studying carbon-carbon bond formation in organic reactions.

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