(2-Bromo-3-methylphenyl)methanol

95%

Reagent Code: #149076
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CAS Number 168886-97-3

science Other reagents with same CAS 168886-97-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.0605 g/mol
Formula C₈H₉BrO
badge Registry Numbers
MDL Number MFCD16659614
thermostat Physical Properties
Boiling Point 277.315 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.481±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the preparation of active ingredients requiring substituted benzyl moieties. Its bromo and hydroxyl functional groups allow for selective transformations, such as cross-coupling reactions or ether formations, making it valuable in building complex organic molecules. Commonly employed in research and development for drug discovery and in the production of specialty chemicals.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to off-white solid
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿258.50
inventory 1g
10-20 days ฿1,490.00
inventory 5g
10-20 days ฿7,250.00

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(2-Bromo-3-methylphenyl)methanol
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the preparation of active ingredients requiring substituted benzyl moieties. Its bromo and hydroxyl functional groups allow for selective transformations, such as cross-coupling reactions or ether formations, making it valuable in building complex organic molecules. Commonly employed in research and development for drug discovery and in the production of specialty chemicals.

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the preparation of active ingredients requiring substituted benzyl moieties. Its bromo and hydroxyl functional groups allow for selective transformations, such as cross-coupling reactions or ether formations, making it valuable in building complex organic molecules. Commonly employed in research and development for drug discovery and in the production of specialty chemicals.

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