Benzo[b]thiophen-2-yl(5-bromo-2-fluorophenyl)methanol

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Reagent Code: #123144
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CAS Number 1034305-11-7

science Other reagents with same CAS 1034305-11-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 337.21 g/mol
Formula C₁₅H₁₀BrFOS
badge Registry Numbers
MDL Number MFCD28347651
thermostat Physical Properties
Boiling Point 458.7±40.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed away from light

description Product Description

This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active molecules, particularly those targeting therapeutic applications. Its structure, featuring both a benzo[b]thiophene and a substituted phenyl ring, makes it valuable for designing compounds with potential anti-inflammatory, antimicrobial, or anticancer properties. Researchers often employ it in the synthesis of complex molecules to study structure-activity relationships and optimize drug efficacy. Additionally, its functional groups allow for further chemical modifications, enabling the creation of diverse derivatives for screening in drug discovery programs.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿26,028.00
inventory 1g
10-20 days ฿5,733.00
inventory 100mg
10-20 days ฿1,251.00
inventory 250mg
10-20 days ฿2,124.00

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Benzo[b]thiophen-2-yl(5-bromo-2-fluorophenyl)methanol
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This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active molecules, particularly those targeting therapeutic applications. Its structure, featuring both a benzo[b]thiophene and a substituted phenyl ring, makes it valuable for designing compounds with potential anti-inflammatory, antimicrobial, or anticancer properties. Researchers often employ it in the synthesis of complex molecules to study structure-activity relationships and optimize drug efficacy. Additionally, its functional groups allow for further chemical modifications, enabling the creation of diverse derivatives for screening in drug discovery programs.
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