4-(Methoxycarbonyl)-2-nitrobenzoic acid

95%

Reagent Code: #65982
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CAS Number 55737-66-1

science Other reagents with same CAS 55737-66-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.16 g/mol
Formula C₉H₇NO₆
badge Registry Numbers
MDL Number MFCD06203344
thermostat Physical Properties
Boiling Point 393.5 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

This compound is primarily utilized in organic synthesis as an intermediate for the production of various pharmaceuticals and agrochemicals. Its structure, featuring both a nitro group and a methoxycarbonyl group, makes it a versatile building block in the development of complex molecules. It is often employed in the synthesis of active pharmaceutical ingredients (APIs) where the nitro group can be reduced to an amine, enabling further functionalization. Additionally, its benzoic acid derivative nature allows it to participate in esterification and amidation reactions, which are crucial in drug design and development. In agrochemical research, it serves as a precursor for creating compounds with potential herbicidal or pesticidal properties. Its role in these fields highlights its importance in advancing both medicinal and agricultural chemistry.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,935.00
inventory 5g
10-20 days ฿6,696.00
inventory 25g
10-20 days ฿17,883.00

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4-(Methoxycarbonyl)-2-nitrobenzoic acid
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This compound is primarily utilized in organic synthesis as an intermediate for the production of various pharmaceuticals and agrochemicals. Its structure, featuring both a nitro group and a methoxycarbonyl group, makes it a versatile building block in the development of complex molecules. It is often employed in the synthesis of active pharmaceutical ingredients (APIs) where the nitro group can be reduced to an amine, enabling further functionalization. Additionally, its benzoic acid derivative nature a

This compound is primarily utilized in organic synthesis as an intermediate for the production of various pharmaceuticals and agrochemicals. Its structure, featuring both a nitro group and a methoxycarbonyl group, makes it a versatile building block in the development of complex molecules. It is often employed in the synthesis of active pharmaceutical ingredients (APIs) where the nitro group can be reduced to an amine, enabling further functionalization. Additionally, its benzoic acid derivative nature allows it to participate in esterification and amidation reactions, which are crucial in drug design and development. In agrochemical research, it serves as a precursor for creating compounds with potential herbicidal or pesticidal properties. Its role in these fields highlights its importance in advancing both medicinal and agricultural chemistry.

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