2-(Methoxycarbonyl)-6-nitrobenzoic Acid

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Reagent Code: #172811
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CAS Number 21606-04-2

science Other reagents with same CAS 21606-04-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.15 g/mol
Formula C₉H₇NO₆
badge Registry Numbers
MDL Number MFCD00034781
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the preparation of active pharmaceutical ingredients (APIs) where nitroaromatic and carboxylic functional groups are required. Its structure allows for further chemical modifications, such as reduction of the nitro group or ester hydrolysis, enabling the development of complex organic molecules. Commonly employed in research settings for constructing heterocyclic compounds and in the development of dyes and specialty polymers due to its electron-withdrawing substituents and reactivity profile.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿150.00
5g
10-20 days ฿162.00
25g
10-20 days ฿330.00
100g
10-20 days ฿1,050.00
500g
10-20 days ฿4,820.00
2-(Methoxycarbonyl)-6-nitrobenzoic Acid
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Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the preparation of active pharmaceutical ingredients (APIs) where nitroaromatic and carboxylic functional groups are required. Its structure allows for further chemical modifications, such as reduction of the nitro group or ester hydrolysis, enabling the development of complex organic molecules. Commonly employed in research settings for constructing heterocyclic compounds and in the development of dyes and sp

Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the preparation of active pharmaceutical ingredients (APIs) where nitroaromatic and carboxylic functional groups are required. Its structure allows for further chemical modifications, such as reduction of the nitro group or ester hydrolysis, enabling the development of complex organic molecules. Commonly employed in research settings for constructing heterocyclic compounds and in the development of dyes and specialty polymers due to its electron-withdrawing substituents and reactivity profile.

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