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

92%

Reagent Code: #148896
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CAS Number 2228656-15-1

science Other reagents with same CAS 2228656-15-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 267.07 g/mol
Formula C₉H₉BrF₂O₂
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure, featuring a 4-bromo-3-methoxyphenyl group and a 2,2-difluoroethan-1-ol moiety, supports selective binding to enzyme active sites, enhances metabolic stability, and improves cell permeability, thereby enhancing drug efficacy. Also utilized in agrochemical research for designing bioactive molecules with improved metabolic stability and bioavailability. The bromo group enables further functionalization via cross-coupling reactions, while the methoxy and difluoro groups contribute to lipophilicity and chemical stability, making it valuable in medicinal chemistry for building complex molecules.

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Test Parameter Specification
Appearance Yellow oily liquid
Purity (%) 92-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,740.00
inventory 250mg
10-20 days ฿6,170.00
inventory 1g
10-20 days ฿15,400.00

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2-(4-bromo-3-methoxyphenyl)-2,2-difluoroethan-1-ol
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure, featuring a 4-bromo-3-methoxyphenyl group and a 2,2-difluoroethan-1-ol moiety, supports selective binding to enzyme active sites, enhances metabolic stability, and improves cell permeability, thereby enhancing drug efficacy. Also utilized in agrochemical research for designing bioactive molecules with improved metabolic stability and bioavailab

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure, featuring a 4-bromo-3-methoxyphenyl group and a 2,2-difluoroethan-1-ol moiety, supports selective binding to enzyme active sites, enhances metabolic stability, and improves cell permeability, thereby enhancing drug efficacy. Also utilized in agrochemical research for designing bioactive molecules with improved metabolic stability and bioavailability. The bromo group enables further functionalization via cross-coupling reactions, while the methoxy and difluoro groups contribute to lipophilicity and chemical stability, making it valuable in medicinal chemistry for building complex molecules.

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