1-Ethyl-2-methyl-1H-indole

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Reagent Code: #182398
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CAS Number 40876-94-6

science Other reagents with same CAS 40876-94-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 159.23 g/mol
Formula C₁₁H₁₃N
badge Registry Numbers
MDL Number MFCD01632168
thermostat Physical Properties
Boiling Point 274.5°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of pharmaceuticals and bioactive molecules. Its indole structure makes it valuable in developing compounds with biological activity, particularly in the research of central nervous system agents. It is also employed in the synthesis of dyes and fluorescent probes due to its aromatic and electron-rich properties. In medicinal chemistry, derivatives based on this scaffold are explored for their potential as anti-inflammatory, antimicrobial, and anticancer agents. Additionally, it finds use in agrochemical research for developing new crop protection agents.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿600.00

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1-Ethyl-2-methyl-1H-indole
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Used primarily in organic synthesis, this compound serves as a key intermediate in the production of pharmaceuticals and bioactive molecules. Its indole structure makes it valuable in developing compounds with biological activity, particularly in the research of central nervous system agents. It is also employed in the synthesis of dyes and fluorescent probes due to its aromatic and electron-rich properties. In medicinal chemistry, derivatives based on this scaffold are explored for their potential as an

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of pharmaceuticals and bioactive molecules. Its indole structure makes it valuable in developing compounds with biological activity, particularly in the research of central nervous system agents. It is also employed in the synthesis of dyes and fluorescent probes due to its aromatic and electron-rich properties. In medicinal chemistry, derivatives based on this scaffold are explored for their potential as anti-inflammatory, antimicrobial, and anticancer agents. Additionally, it finds use in agrochemical research for developing new crop protection agents.

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