7-Bromo-2-chlorobenzo[d]thiazole

≥95%

Reagent Code: #120858
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CAS Number 1188227-29-3

science Other reagents with same CAS 1188227-29-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 248.53 g/mol
Formula C₇H₃BrClNS
badge Registry Numbers
MDL Number MFCD09749230
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various heterocyclic compounds. Its structure, featuring both bromo and chloro substituents, makes it a versatile building block for constructing more complex molecules, particularly in the development of pharmaceuticals and agrochemicals. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to introduce functional groups or create novel compounds with potential biological activity. Additionally, its benzo[d]thiazole core is of interest in materials science for designing organic electronic materials or fluorescent dyes due to its electron-rich aromatic system.

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Test Parameter Specification
Appearance Off White Powder
Purity (%) 95-100
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿11,763.00
inventory 250mg
10-20 days ฿5,877.00

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7-Bromo-2-chlorobenzo[d]thiazole
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This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various heterocyclic compounds. Its structure, featuring both bromo and chloro substituents, makes it a versatile building block for constructing more complex molecules, particularly in the development of pharmaceuticals and agrochemicals. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to introduce functional groups or create no

This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various heterocyclic compounds. Its structure, featuring both bromo and chloro substituents, makes it a versatile building block for constructing more complex molecules, particularly in the development of pharmaceuticals and agrochemicals. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to introduce functional groups or create novel compounds with potential biological activity. Additionally, its benzo[d]thiazole core is of interest in materials science for designing organic electronic materials or fluorescent dyes due to its electron-rich aromatic system.

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