2-(4-bromo-3-fluorophenyl)-2,2-difluoroethan-1-ol

99%

Reagent Code: #148878
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CAS Number 1823989-97-4

science Other reagents with same CAS 1823989-97-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.03 g/mol
Formula C₈H₆BrF₃O
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its unique halogenated structure enhances binding selectivity to specific enzyme targets. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the presence of multiple halogens that influence metabolic stability and lipophilicity. Also utilized in the preparation of radiolabeled compounds for positron emission tomography (PET) imaging research.

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Test Parameter Specification
Appearance Colorless oil
Purity (%) 98.5-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿7,524.00
inventory 250mg
10-20 days ฿5,260.00

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2-(4-bromo-3-fluorophenyl)-2,2-difluoroethan-1-ol
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Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its unique halogenated structure enhances binding selectivity to specific enzyme targets. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the presence of multiple halogens that influence metabolic stability and lipophilicity. Also utilized in the preparation of radiolabeled compounds for positron emission t

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its unique halogenated structure enhances binding selectivity to specific enzyme targets. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the presence of multiple halogens that influence metabolic stability and lipophilicity. Also utilized in the preparation of radiolabeled compounds for positron emission tomography (PET) imaging research.

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