2-Chloro-5-nitrobenzo[d]thiazole

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Reagent Code: #160274
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CAS Number 3622-38-6

science Other reagents with same CAS 3622-38-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.63 g/mol
Formula C₇H₃ClN₂O₂S
thermostat Physical Properties
Boiling Point 348.1°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of fluorescent dyes and optical brighteners for textiles and paper. Plays a role in the production of agrochemicals, particularly herbicides and fungicides, due to its reactivity and stability in chlorinated aromatic systems. Also employed in the development of sulfur-containing heterocyclic compounds for pharmaceutical research, especially in the design of antimicrobial and anti-inflammatory agents. Its nitro and chloro functional groups allow for sequential substitution reactions, making it valuable in fine chemical synthesis and material science applications.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,110.00

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2-Chloro-5-nitrobenzo[d]thiazole
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Used as an intermediate in the synthesis of fluorescent dyes and optical brighteners for textiles and paper. Plays a role in the production of agrochemicals, particularly herbicides and fungicides, due to its reactivity and stability in chlorinated aromatic systems. Also employed in the development of sulfur-containing heterocyclic compounds for pharmaceutical research, especially in the design of antimicrobial and anti-inflammatory agents. Its nitro and chloro functional groups allow for sequential subs

Used as an intermediate in the synthesis of fluorescent dyes and optical brighteners for textiles and paper. Plays a role in the production of agrochemicals, particularly herbicides and fungicides, due to its reactivity and stability in chlorinated aromatic systems. Also employed in the development of sulfur-containing heterocyclic compounds for pharmaceutical research, especially in the design of antimicrobial and anti-inflammatory agents. Its nitro and chloro functional groups allow for sequential substitution reactions, making it valuable in fine chemical synthesis and material science applications.

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