5-(tert-Butyl)-2-nitroaniline

98%

Reagent Code: #155731
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CAS Number 142564-53-2

science Other reagents with same CAS 142564-53-2

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scatter_plot Molecular Information
Weight 194.23 g/mol
Formula C₁₀H₁₄N₂O₂
badge Registry Numbers
MDL Number MFCD01463636
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of dyes and pigments, particularly in the production of azo dyes which are widely applied in the textile, printing, and coating industries. It also serves as a building block in the manufacture of certain agrochemicals and pharmaceuticals where nitroaromatic compounds are required. Its tert-butyl and nitro functional groups make it suitable for further chemical modifications in organic synthesis. Due to the presence of the aromatic amine and nitro group, it can participate in reduction and coupling reactions to form complex molecules. Handle with care as aromatic amines may pose health and safety risks.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,490.00
inventory 250mg
10-20 days ฿15,890.00

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5-(tert-Butyl)-2-nitroaniline
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Used as an intermediate in the synthesis of dyes and pigments, particularly in the production of azo dyes which are widely applied in the textile, printing, and coating industries. It also serves as a building block in the manufacture of certain agrochemicals and pharmaceuticals where nitroaromatic compounds are required. Its tert-butyl and nitro functional groups make it suitable for further chemical modifications in organic synthesis. Due to the presence of the aromatic amine and nitro group, it can pa

Used as an intermediate in the synthesis of dyes and pigments, particularly in the production of azo dyes which are widely applied in the textile, printing, and coating industries. It also serves as a building block in the manufacture of certain agrochemicals and pharmaceuticals where nitroaromatic compounds are required. Its tert-butyl and nitro functional groups make it suitable for further chemical modifications in organic synthesis. Due to the presence of the aromatic amine and nitro group, it can participate in reduction and coupling reactions to form complex molecules. Handle with care as aromatic amines may pose health and safety risks.

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