2-Bromo-6-methoxybenzothiazole

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Reagent Code: #144715
label
Alias 2-Bromo-6-methoxybenzo[D]thiazole; 6-methoxy-2-bromobenzothiazole
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CAS Number 2941-58-4

science Other reagents with same CAS 2941-58-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.11 g/mol
Formula C₈H₆BrNOS
badge Registry Numbers
MDL Number MFCD08459026
thermostat Physical Properties
Boiling Point 335.4±34.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.666±0.06 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antitumor and antimicrobial agents. It serves as a building block in organic reactions where the bromine atom allows for further functionalization through cross-coupling reactions such as Suzuki or Heck reactions. Its structure is valuable in medicinal chemistry for modifying benzothiazole-based compounds to enhance biological activity. Also employed in the preparation of fluorescent dyes and optoelectronic materials due to the inherent electronic properties of the benzothiazole core.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿340.00
inventory 1g
10-20 days ฿530.00
inventory 25g
10-20 days ฿6,920.00
inventory 5g
10-20 days ฿1,820.00

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2-Bromo-6-methoxybenzothiazole
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antitumor and antimicrobial agents. It serves as a building block in organic reactions where the bromine atom allows for further functionalization through cross-coupling reactions such as Suzuki or Heck reactions. Its structure is valuable in medicinal chemistry for modifying benzothiazole-based compounds to enhance biological activity. Also employed in the preparation of fluorescent dyes and optoelectronic ma

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antitumor and antimicrobial agents. It serves as a building block in organic reactions where the bromine atom allows for further functionalization through cross-coupling reactions such as Suzuki or Heck reactions. Its structure is valuable in medicinal chemistry for modifying benzothiazole-based compounds to enhance biological activity. Also employed in the preparation of fluorescent dyes and optoelectronic materials due to the inherent electronic properties of the benzothiazole core.

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