4-Bromo-2,6-difluorobenzyl alcohol

97%

Reagent Code: #143532
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CAS Number 162744-59-4

science Other reagents with same CAS 162744-59-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.01 g/mol
Formula F₂C₆H₂(Br)CH₂OH
badge Registry Numbers
MDL Number MFCD03094461
thermostat Physical Properties
Melting Point 76-81 °C(lit.)
Boiling Point 250℃
inventory_2 Storage & Handling
Density 1.744
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its structure allows for selective functionalization, making it valuable in creating active ingredients with improved environmental stability and target specificity. Also employed in the preparation of fluorinated building blocks for drug discovery, where the bromo and hydroxyl groups enable further chemical modifications through cross-coupling or esterification reactions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿174.00
inventory 5g
10-20 days ฿690.00
inventory 25g
10-20 days ฿3,380.00
inventory 100g
10-20 days ฿13,350.00

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4-Bromo-2,6-difluorobenzyl alcohol
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Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its structure allows for selective functionalization, making it valuable in creating active ingredients with improved environmental stability and target specificity. Also employed in the preparation of fluorinated building blocks for drug discovery, where the bromo and hydroxyl groups enable further chemical modifications through cross-coupling or esterification

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its structure allows for selective functionalization, making it valuable in creating active ingredients with improved environmental stability and target specificity. Also employed in the preparation of fluorinated building blocks for drug discovery, where the bromo and hydroxyl groups enable further chemical modifications through cross-coupling or esterification reactions.

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