5-Fluoro-2-methylbenzyl bromide

98%

Reagent Code: #119876
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CAS Number 261951-71-7

science Other reagents with same CAS 261951-71-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.05 g/mol
Formula C₈H₈BrF
badge Registry Numbers
MDL Number MFCD01631528
thermostat Physical Properties
Boiling Point 86°C/3mm
inventory_2 Storage & Handling
Density 1.456
Storage room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It is valuable in the development of compounds with potential therapeutic properties, such as anti-inflammatory or anticancer agents. The compound’s reactive benzyl bromide group allows it to participate in alkylation reactions, making it useful for modifying molecular structures. Additionally, it can be employed in the synthesis of advanced materials or specialty chemicals where fluorine substitution is required for specific properties like stability or bioavailability.

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Test Parameter Specification
Purity (GC) 97.5-100
Refractive Index (N20/D) 1.547-1.551
Specific Gravity (20/20) 1.473-1.477
Appearance Colorless Liquid
Infrared Spectrum Conforms To Structure
Proton NMR Spectrum Conforms To Structure

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inventory 1g
10-20 days ฿1,200.00

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5-Fluoro-2-methylbenzyl bromide
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Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It is valuable in the development of compounds with potential therapeutic properties, such as anti-inflammatory or anticancer agents. The compound’s reactive benzyl bromide group allows it to participate in alkylation reactions, making it useful for modifying molecular structures. Additionally, it can be employed in the synthesis of advanced materials or specialty chemicals where fluorine su

Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It is valuable in the development of compounds with potential therapeutic properties, such as anti-inflammatory or anticancer agents. The compound’s reactive benzyl bromide group allows it to participate in alkylation reactions, making it useful for modifying molecular structures. Additionally, it can be employed in the synthesis of advanced materials or specialty chemicals where fluorine substitution is required for specific properties like stability or bioavailability.

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