N-(p-Tolyl)benzo[d]thiazol-2-amine

95%

Reagent Code: #220218
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CAS Number 70785-26-1

science Other reagents with same CAS 70785-26-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 240.32 g/mol
Formula C₁₄H₁₂N₂S
badge Registry Numbers
MDL Number MFCD01830676
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals and agrochemicals. Its structure supports the development of compounds with antimicrobial, antifungal, and anti-inflammatory properties. Commonly employed in medicinal chemistry for designing kinase inhibitors and fluorescent probes due to the strong electron-withdrawing nature of the benzothiazole ring and the stability provided by the toluidine moiety. Also utilized in materials science for developing organic semiconductors and luminescent materials.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,370.00
inventory 1g
10-20 days ฿15,210.00
inventory 5g
10-20 days ฿62,080.00

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N-(p-Tolyl)benzo[d]thiazol-2-amine
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals and agrochemicals. Its structure supports the development of compounds with antimicrobial, antifungal, and anti-inflammatory properties. Commonly employed in medicinal chemistry for designing kinase inhibitors and fluorescent probes due to the strong electron-withdrawing nature of the benzothiazole ring and the stability provided by the toluidine moiety. Also utilized in materials science for dev

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals and agrochemicals. Its structure supports the development of compounds with antimicrobial, antifungal, and anti-inflammatory properties. Commonly employed in medicinal chemistry for designing kinase inhibitors and fluorescent probes due to the strong electron-withdrawing nature of the benzothiazole ring and the stability provided by the toluidine moiety. Also utilized in materials science for developing organic semiconductors and luminescent materials.

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