2-(Bromomethyl)-5-fluorobenzo[d]thiazole

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Reagent Code: #140898
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CAS Number 143163-70-6

science Other reagents with same CAS 143163-70-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 246.1 g/mol
Formula C₈H₅NFSBr
badge Registry Numbers
MDL Number MFCD03428526
thermostat Physical Properties
Boiling Point 292.9±20.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.758±0.06 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and biologically active compounds. Its structure supports the development of fluorinated benzothiazole derivatives, which are of interest in medicinal chemistry due to their potential anticancer, antimicrobial, and anti-inflammatory properties. The bromomethyl group allows for easy functionalization through nucleophilic substitution, making it valuable in building more complex molecules for drug discovery. It is also employed in the preparation of fluorescent probes and labeled compounds for biochemical assays and imaging studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,640.00
inventory 250mg
10-20 days ฿12,990.00
inventory 1g
10-20 days ฿35,070.00

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2-(Bromomethyl)-5-fluorobenzo[d]thiazole
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Used primarily as an intermediate in the synthesis of pharmaceuticals and biologically active compounds. Its structure supports the development of fluorinated benzothiazole derivatives, which are of interest in medicinal chemistry due to their potential anticancer, antimicrobial, and anti-inflammatory properties. The bromomethyl group allows for easy functionalization through nucleophilic substitution, making it valuable in building more complex molecules for drug discovery. It is also employed in the pr

Used primarily as an intermediate in the synthesis of pharmaceuticals and biologically active compounds. Its structure supports the development of fluorinated benzothiazole derivatives, which are of interest in medicinal chemistry due to their potential anticancer, antimicrobial, and anti-inflammatory properties. The bromomethyl group allows for easy functionalization through nucleophilic substitution, making it valuable in building more complex molecules for drug discovery. It is also employed in the preparation of fluorescent probes and labeled compounds for biochemical assays and imaging studies.

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