Ethyl 5-acetoxy-6-bromo-2-(bromomethyl)-1-methyl-1H-indole-3-carboxylate

98%

Reagent Code: #184792
label
Alias Ethyl 1-methyl-2-(bromomethyl)-5-acetoxy-6-bromoindole-3-carboxylate
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CAS Number 110543-98-1

science Other reagents with same CAS 110543-98-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 433.09 g/mol
Formula C₁₅H₁₅Br₂NO₄
badge Registry Numbers
MDL Number MFCD00407019
thermostat Physical Properties
Melting Point 179-180 °C
Boiling Point 529.8 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of indole-based pharmaceutical compounds, particularly in the development of serotonin receptor modulators and anti-inflammatory agents. Its functional groups enable selective transformations for constructing complex heterocyclic systems. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its reactive bromomethyl and acetoxy sites. Also utilized in the preparation of fluorescent probes and bioactive molecule derivatives through cross-coupling and nucleophilic substitution reactions.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿1,070.00
inventory 100g
10-20 days ฿3,640.00

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Ethyl 5-acetoxy-6-bromo-2-(bromomethyl)-1-methyl-1H-indole-3-carboxylate
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Used as a key intermediate in the synthesis of indole-based pharmaceutical compounds, particularly in the development of serotonin receptor modulators and anti-inflammatory agents. Its functional groups enable selective transformations for constructing complex heterocyclic systems. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its reactive bromomethyl and acetoxy sites. Also utilized in the preparation of fluorescent probes and bioactive molecule derivatives

Used as a key intermediate in the synthesis of indole-based pharmaceutical compounds, particularly in the development of serotonin receptor modulators and anti-inflammatory agents. Its functional groups enable selective transformations for constructing complex heterocyclic systems. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its reactive bromomethyl and acetoxy sites. Also utilized in the preparation of fluorescent probes and bioactive molecule derivatives through cross-coupling and nucleophilic substitution reactions.

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