N-(2,3-dimethyl-6-nitrophenyl)acetamide

≥95%

Reagent Code: #216586
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CAS Number 138330-47-9

science Other reagents with same CAS 138330-47-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 208.21 g/mol
Formula C₁₀H₁₂N₂O₃
badge Registry Numbers
MDL Number MFCD00157612
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 development of azo dyes for textiles and printing inks. It also serves in the preparation of certain pharmaceuticals where nitro-substituted aromatic acetamides act as precursors in drug synthesis. Its structure allows for further functionalization through reduction of the nitro group, enabling the formation of amine derivatives important in agrochemicals and medicinal chemistry. Additionally, it finds use in research settings for studying electrophilic substitution reactions in hindered aromatic systems.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿16,130.00
N-(2,3-dimethyl-6-nitrophenyl)acetamide
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Used as an intermediate in the synthesis of dyes and pigments, particularly in the development of azo dyes for textiles and printing inks. It also serves in the preparation of certain pharmaceuticals where nitro-substituted aromatic acetamides act as precursors in drug synthesis. Its structure allows for further functionalization through reduction of the nitro group, enabling the formation of amine derivatives important in agrochemicals and medicinal chemistry. Additionally, it finds use in research sett

Used as an intermediate in the synthesis of dyes and pigments, particularly in the development of azo dyes for textiles and printing inks. It also serves in the preparation of certain pharmaceuticals where nitro-substituted aromatic acetamides act as precursors in drug synthesis. Its structure allows for further functionalization through reduction of the nitro group, enabling the formation of amine derivatives important in agrochemicals and medicinal chemistry. Additionally, it finds use in research settings for studying electrophilic substitution reactions in hindered aromatic systems.

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