62-23-7
62-23-7
Chemical Structure
4-Nitrobenzoic acid
- CAS No.: 62-23-7
- Formula:C7H5NO4
- Molecular Weight:167.12
IUPAC Name: 4-nitrobenzoic acid
InChIKey: OTLNPYWUJOZPPA-UHFFFAOYSA-N
SMILES: O=C(O)C1=CC=C([N+]([O-])=O)C=C1
Biological Activity: 4-Nitrobenzoic acid is a nitroaromatic compound that can be used in the synthesis of other active compounds. 4-Nitrobenzoic acid is also an inhibitor agent, which can be used for the recognition of the Mycobacterium tuberculosis complex and differentiation from non-tuberculous mycobacteria[1].
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4-Nitrobenzoic acid | 99.84% | 4-Nitrobenzoic acid is a nitroaromatic compound that can be used in the synthesis of other active compounds. 4-Nitrobenzoic acid is also an inhibitor agent, which can be used for the recognition of the Mycobacterium tuberculosis complex and differentiation from non-tuberculous mycobacteria. | ||||||||||||||||||||
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4-Nitrobenzoic acid (Standard) | ≥98% | 4-Nitrobenzoic acid (Standard) is the analytical standard of 4-Nitrobenzoic acid (HY-Y0607). This product is intended for research and analytical applications. 4-Nitrobenzoic acid is an oxidoreduction mediator and an electron transfer promoter. 4-Nitrobenzoic acid accepts electrons from the reduced glucose oxidase and transfers them to the electrode to promote the glucose oxidation reaction, while minimizing the formation of protonated amine groups. | ||||||||||||||||||||
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4-Nitrobenzoic acid-d2 | 99% | 4-Nitrobenzoic acid-d2 is the deuterium labeled 4-Nitrobenzoic acid (HY-Y0607). 4-Nitrobenzoic acid acts as a redox mediator and electron transfer promoter. 4-Nitrobenzoic acid accepts electrons from reduced glucose oxidase and transfers them to the electrode to facilitate the glucose oxidation reaction, while minimizing the formation of protonated amino groups. | ||||||||||||||||||||
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4-Nitrobenzoic acid-d4 | 4-Nitrobenzoic acid-d4 is the deuterium labeled 4-Nitrobenzoic acid (HY-Y0607). 4-Nitrobenzoic acid is an oxidoreduction mediator and an electron transfer promoter. 4-Nitrobenzoic acid accepts electrons from the reduced glucose oxidase and transfers them to the electrode to promote the glucose oxidation reaction, while minimizing the formation of protonated amine groups. | |||||||||||||||||||||
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References
