2-(Ethylsulfonyl)aniline

≥95%

Reagent Code: #183692
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CAS Number 31596-87-9

science Other reagents with same CAS 31596-87-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 185.24 g/mol
Formula C₈H₁₁NO₂S
badge Registry Numbers
MDL Number MFCD09945923
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in inert gas

description Product Description

Used as an intermediate in the synthesis of dyes and pigments, particularly in the production of sulfur-based dyes for textiles. Also serves as a building block in agrochemicals for developing herbicides and fungicides. Its sulfone-aniline structure makes it valuable in pharmaceutical research, especially in creating compounds with anti-inflammatory and antimicrobial activity. Additionally, it is employed in the development of specialty polymers and photoresists due to its thermal stability and electron-withdrawing properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,180.00
inventory 1g
10-20 days ฿15,530.00
2-(Ethylsulfonyl)aniline
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Used as an intermediate in the synthesis of dyes and pigments, particularly in the production of sulfur-based dyes for textiles. Also serves as a building block in agrochemicals for developing herbicides and fungicides. Its sulfone-aniline structure makes it valuable in pharmaceutical research, especially in creating compounds with anti-inflammatory and antimicrobial activity. Additionally, it is employed in the development of specialty polymers and photoresists due to its thermal stability and electron-

Used as an intermediate in the synthesis of dyes and pigments, particularly in the production of sulfur-based dyes for textiles. Also serves as a building block in agrochemicals for developing herbicides and fungicides. Its sulfone-aniline structure makes it valuable in pharmaceutical research, especially in creating compounds with anti-inflammatory and antimicrobial activity. Additionally, it is employed in the development of specialty polymers and photoresists due to its thermal stability and electron-withdrawing properties.

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