Methyl 7-bromo-3-oxo-2,3-dihydro-1H-indene-5-carboxylate

≥95%

Reagent Code: #120870
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CAS Number 1951439-41-0

science Other reagents with same CAS 1951439-41-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.09 g/mol
Formula C₁₁H₉BrO₃
badge Registry Numbers
MDL Number MFCD28404709
thermostat Physical Properties
Boiling Point 397.8°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This chemical is primarily utilized in organic synthesis as a key intermediate for the development of complex molecules. Its structure, featuring both a bromo and ester functional group, makes it a versatile building block in the synthesis of pharmaceuticals and agrochemicals. It is often employed in cross-coupling reactions, such as Suzuki or Heck reactions, to create more elaborate compounds. Additionally, its indene core is valuable in the design of materials with specific electronic or optical properties, making it useful in the field of material science. Researchers also explore its potential in the synthesis of bioactive compounds, particularly in the development of anti-inflammatory or anticancer agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,853.00
inventory 250mg
10-20 days ฿23,706.00

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Methyl 7-bromo-3-oxo-2,3-dihydro-1H-indene-5-carboxylate
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This chemical is primarily utilized in organic synthesis as a key intermediate for the development of complex molecules. Its structure, featuring both a bromo and ester functional group, makes it a versatile building block in the synthesis of pharmaceuticals and agrochemicals. It is often employed in cross-coupling reactions, such as Suzuki or Heck reactions, to create more elaborate compounds. Additionally, its indene core is valuable in the design of materials with specific electronic or optical proper

This chemical is primarily utilized in organic synthesis as a key intermediate for the development of complex molecules. Its structure, featuring both a bromo and ester functional group, makes it a versatile building block in the synthesis of pharmaceuticals and agrochemicals. It is often employed in cross-coupling reactions, such as Suzuki or Heck reactions, to create more elaborate compounds. Additionally, its indene core is valuable in the design of materials with specific electronic or optical properties, making it useful in the field of material science. Researchers also explore its potential in the synthesis of bioactive compounds, particularly in the development of anti-inflammatory or anticancer agents.

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