4-Nitrophthalamide

97%

Reagent Code: #217148
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CAS Number 13138-53-9

science Other reagents with same CAS 13138-53-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 209.16 g/mol
Formula C₈H₇N₃O₄
badge Registry Numbers
MDL Number MFCD00052702
thermostat Physical Properties
Melting Point 195°C dec. (Lit.)
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used primarily as an intermediate in the synthesis of dyes and pigments, 4-Nitrophthalamide plays a key role in the production of high-performance colorants for textiles and inks. Its structure allows for further chemical modifications, making it valuable in the development of photoactive compounds and fluorescent dyes. It is also employed in the preparation of certain pharmaceuticals and agrochemicals, where the nitro group can be reduced to an amine for subsequent coupling reactions. Additionally, it has been explored in research settings for the development of sensors and functional materials due to its electron-withdrawing properties and ability to participate in hydrogen bonding.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿150.00
5g
10-20 days ฿590.00
25g
10-20 days ฿2,900.00
4-Nitrophthalamide
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Used primarily as an intermediate in the synthesis of dyes and pigments, 4-Nitrophthalamide plays a key role in the production of high-performance colorants for textiles and inks. Its structure allows for further chemical modifications, making it valuable in the development of photoactive compounds and fluorescent dyes. It is also employed in the preparation of certain pharmaceuticals and agrochemicals, where the nitro group can be reduced to an amine for subsequent coupling reactions. Additionally, it h

Used primarily as an intermediate in the synthesis of dyes and pigments, 4-Nitrophthalamide plays a key role in the production of high-performance colorants for textiles and inks. Its structure allows for further chemical modifications, making it valuable in the development of photoactive compounds and fluorescent dyes. It is also employed in the preparation of certain pharmaceuticals and agrochemicals, where the nitro group can be reduced to an amine for subsequent coupling reactions. Additionally, it has been explored in research settings for the development of sensors and functional materials due to its electron-withdrawing properties and ability to participate in hydrogen bonding.

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