Methyl5-bromo-2,3-dihydro-1H-indene-2-carboxylate

98%

Reagent Code: #213338
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CAS Number 628732-09-2

science Other reagents with same CAS 628732-09-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.11 g/mol
Formula C₁₁H₁₁BrO₂
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its structure allows functionalization at multiple sites, making it valuable in constructing complex molecules, particularly in the development of central nervous system agents and anti-inflammatory drugs. The bromine substituent enables cross-coupling reactions, such as Suzuki or Heck reactions, for building carbon-carbon bonds. The ester group can be hydrolyzed to the corresponding carboxylic acid or reduced to an alcohol, offering versatility in derivatization. Commonly employed in medicinal chemistry for scaffold modification and structure-activity relationship studies.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿15,760.00
Methyl5-bromo-2,3-dihydro-1H-indene-2-carboxylate
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Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its structure allows functionalization at multiple sites, making it valuable in constructing complex molecules, particularly in the development of central nervous system agents and anti-inflammatory drugs. The bromine substituent enables cross-coupling reactions, such as Suzuki or Heck reactions, for building carbon-carbon bonds. The ester group can be hydrolyzed to the corresponding carboxylic acid or reduced to an

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its structure allows functionalization at multiple sites, making it valuable in constructing complex molecules, particularly in the development of central nervous system agents and anti-inflammatory drugs. The bromine substituent enables cross-coupling reactions, such as Suzuki or Heck reactions, for building carbon-carbon bonds. The ester group can be hydrolyzed to the corresponding carboxylic acid or reduced to an alcohol, offering versatility in derivatization. Commonly employed in medicinal chemistry for scaffold modification and structure-activity relationship studies.

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