Methyl 1-(4-(bromomethyl)phenyl)cyclopropanecarboxylate

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Reagent Code: #214405
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CAS Number 873372-30-6

science Other reagents with same CAS 873372-30-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.138 g/mol
Formula C₁₂H₁₃BrO₂
badge Registry Numbers
MDL Number MFCD28347493
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where a cyclopropane ring and a bromomethylbenzene moiety are required. The bromine atom serves as a reactive handle for further functionalization through cross-coupling reactions or nucleophilic substitution, enabling the construction of complex molecules. Its ester group allows for easy transformation into carboxylic acids or amides, making it valuable in medicinal chemistry for optimizing drug candidates. Commonly employed in research settings for the preparation of analogs in structure-activity relationship (SAR) studies.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿22,150.00
Methyl 1-(4-(bromomethyl)phenyl)cyclopropanecarboxylate
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where a cyclopropane ring and a bromomethylbenzene moiety are required. The bromine atom serves as a reactive handle for further functionalization through cross-coupling reactions or nucleophilic substitution, enabling the construction of complex molecules. Its ester group allows for easy transformation into carboxylic acids or amides, making it valuable in

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where a cyclopropane ring and a bromomethylbenzene moiety are required. The bromine atom serves as a reactive handle for further functionalization through cross-coupling reactions or nucleophilic substitution, enabling the construction of complex molecules. Its ester group allows for easy transformation into carboxylic acids or amides, making it valuable in medicinal chemistry for optimizing drug candidates. Commonly employed in research settings for the preparation of analogs in structure-activity relationship (SAR) studies.

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