5-Bromo-2,3,3-trimethyl-3H-indole

95%

Reagent Code: #149000
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CAS Number 54136-24-2

science Other reagents with same CAS 54136-24-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 238.12 g/mol
Formula C₁₁H₁₂BrN
badge Registry Numbers
MDL Number MFCD07779490
thermostat Physical Properties
Boiling Point 285 °C at 761 mmHg
inventory_2 Storage & Handling
Density 1.37 g/cm4
Storage Room temperature, dry

description Product Description

Used primarily as an intermediate in the synthesis of functional dyes and photochromic compounds. It plays a key role in the development of indole-based dyes for imaging and sensing applications. Its brominated structure allows for further functionalization via cross-coupling reactions, making it valuable in organic electronics and pharmaceutical research. Also employed in the preparation of novel indole derivatives with potential biological activity, including antimicrobial and anticancer agents.

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Test Parameter Specification
Appearance Brown to yellow solid
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿730.00
inventory 5g
10-20 days ฿3,140.00
inventory 25g
10-20 days ฿15,640.00

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5-Bromo-2,3,3-trimethyl-3H-indole
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Used primarily as an intermediate in the synthesis of functional dyes and photochromic compounds. It plays a key role in the development of indole-based dyes for imaging and sensing applications. Its brominated structure allows for further functionalization via cross-coupling reactions, making it valuable in organic electronics and pharmaceutical research. Also employed in the preparation of novel indole derivatives with potential biological activity, including antimicrobial and anticancer agents.

Used primarily as an intermediate in the synthesis of functional dyes and photochromic compounds. It plays a key role in the development of indole-based dyes for imaging and sensing applications. Its brominated structure allows for further functionalization via cross-coupling reactions, making it valuable in organic electronics and pharmaceutical research. Also employed in the preparation of novel indole derivatives with potential biological activity, including antimicrobial and anticancer agents.

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