2, 6-Dichloro-4-nitrobenzo[d]thiazole

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Reagent Code: #178029
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CAS Number 1379329-41-5

science Other reagents with same CAS 1379329-41-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 249.07 g/mol
Formula C₇H₂Cl₂N₂O₂S
badge Registry Numbers
MDL Number MFCD09748627
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as an intermediate in the synthesis of fluorescent dyes and optical brighteners due to its reactive aromatic ring system and electron-withdrawing substituents. It is also employed in the development of agrochemicals, particularly as a building block for herbicides and fungicides. Its nitro and chloro groups allow for selective substitutions, making it valuable in pharmaceutical research for creating bioactive molecules. Additionally, it serves in the preparation of thiazole-based polymers with potential applications in organic electronics.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿8,360.00
inventory 250mg
10-20 days ฿21,330.00

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2, 6-Dichloro-4-nitrobenzo[d]thiazole
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Used as an intermediate in the synthesis of fluorescent dyes and optical brighteners due to its reactive aromatic ring system and electron-withdrawing substituents. It is also employed in the development of agrochemicals, particularly as a building block for herbicides and fungicides. Its nitro and chloro groups allow for selective substitutions, making it valuable in pharmaceutical research for creating bioactive molecules. Additionally, it serves in the preparation of thiazole-based polymers with poten

Used as an intermediate in the synthesis of fluorescent dyes and optical brighteners due to its reactive aromatic ring system and electron-withdrawing substituents. It is also employed in the development of agrochemicals, particularly as a building block for herbicides and fungicides. Its nitro and chloro groups allow for selective substitutions, making it valuable in pharmaceutical research for creating bioactive molecules. Additionally, it serves in the preparation of thiazole-based polymers with potential applications in organic electronics.

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