I agree Our site saves small pieces of text information (cookies) on your device in order to deliver better content and for statistical purposes. You can disable the usage of cookies by changing the settings of your browser. By browsing our website without changing the browser settings you grant us permission to store that information on your device.
3-Nitrobenzoic acid was used to investigated the role of ozone as additional decomposition or finishing reagent in the degradation of o-, m- and p-nitobenzoic acids
Narender P. Luthra.; R.Bruce Dunlap.; Jerome D. Odom. Characterization of a new sulfhydryl group reagent: 6,6?-Diselenobis-(3-Nitrobenzoic acid), a selenium analog of Ellman's reagent. Analytical Biochemistry. 1981, 117, (1), 94-102.
Henrik Stephensen.; Florencio Zaragoza. Solid-phase synthesis of N-hydroxyindoles and benzo[c]isoxazoles by C-arylation of substituted acetonitriles and 1,3-dicarbonyl compounds with polystyrene-bound aryl fluorides. Tetrahedron Letters. 1999, 40, (31), 5799-5802.
Gefahrenhinweise (EU): H301-H315-H319-H341-H335
Toxic if swallowed. Causes skin irritation. Causes serious eye irritation. Suspected of causing genetic defects. May cause respiratory irritation.
Do not breathe dust/fume/gas/mist/vapours/spray. Obtain special instructions before use. Wear protective gloves. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.