(4-Bromo-2-fluorophenyl)(3,4,5-trimethoxyphenyl)methanone

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Reagent Code: #130228
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CAS Number 1016544-26-5

science Other reagents with same CAS 1016544-26-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 369.18 g/mol
Formula C₁₆H₁₄BrFO₄
thermostat Physical Properties
Boiling Point 481.2±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.420±0.06 g/cm3(Predicted)
Storage Room temperature, seal, inert gas

description Product Description

Used in pharmaceutical research as an intermediate in the synthesis of compounds with potential anticancer activity, particularly those that inhibit cancer cell division through microtubule disruption (microtubule inhibition). Additionally, it is employed in the development of anti-inflammatory and analgesic drugs due to its structural similarity to colchicine analogs, which exhibit significant biological activity in various bodily systems. This compound supports the creation of complex molecules for targeted therapies, enhancing metabolic stability and bioavailability in drug candidates.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿22,710.00
inventory 25g
10-20 days ฿79,500.00
inventory 1g
10-20 days ฿6,490.00

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(4-Bromo-2-fluorophenyl)(3,4,5-trimethoxyphenyl)methanone
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Used in pharmaceutical research as an intermediate in the synthesis of compounds with potential anticancer activity, particularly those that inhibit cancer cell division through microtubule disruption (microtubule inhibition). Additionally, it is employed in the development of anti-inflammatory and analgesic drugs due to its structural similarity to colchicine analogs, which exhibit significant biological activity in various bodily systems. This compound supports the creation of complex molecules for tar

Used in pharmaceutical research as an intermediate in the synthesis of compounds with potential anticancer activity, particularly those that inhibit cancer cell division through microtubule disruption (microtubule inhibition). Additionally, it is employed in the development of anti-inflammatory and analgesic drugs due to its structural similarity to colchicine analogs, which exhibit significant biological activity in various bodily systems. This compound supports the creation of complex molecules for targeted therapies, enhancing metabolic stability and bioavailability in drug candidates.

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