CAS 1429-05-6
:P-NITROBENZOIC ACID PHENYL ESTER
Description:
P-Nitrobenzoic acid phenyl ester, with the CAS number 1429-05-6, is an organic compound characterized by its ester functional group derived from p-nitrobenzoic acid and phenol. This compound typically appears as a crystalline solid and is known for its moderate solubility in organic solvents, while being less soluble in water due to its hydrophobic phenyl group. The presence of the nitro group (-NO2) on the benzene ring contributes to its electron-withdrawing properties, which can influence its reactivity and interactions in chemical reactions. P-Nitrobenzoic acid phenyl ester is often utilized in organic synthesis and as an intermediate in the production of various pharmaceuticals and agrochemicals. Its chemical stability and reactivity make it a valuable compound in research and industrial applications. Additionally, safety precautions should be observed when handling this substance, as nitro compounds can be hazardous and may pose environmental risks.
Formula:C13H9NO4
InChI:InChI=1/C13H9NO4/c15-13(18-12-4-2-1-3-5-12)10-6-8-11(9-7-10)14(16)17/h1-9H
SMILES:c1ccc(cc1)OC(=O)c1ccc(cc1)N(=O)=O
Synonyms:- 4-Nitro-Benzoic Acid Phenyl Ester
- Phenyl 4-Nitrobenzoate
- Phenyl-P-Nitrobenzoate
- P-NITROBENZOIC ACID PHENYL ESTER
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Found 2 products.
Phenyl 4-nitrobenzoate
CAS:<p>Phenyl 4-nitrobenzoate is a polymerized ester with hydroxy groups and phosphorus oxychloride as the raw material. It is synthesized by heating ethyl esters in trifluoroacetic acid, which reacts with nitric acid and phosphorus oxychloride. The compound is an amide with a bond cleavage activation energy of 109 kJ/mol. The kinetic of the reaction was determined by measuring the time it took for the reaction to reach certain levels. Phenyl 4-nitrobenzoate has been shown to be able to activate supramolecular assemblies, leading to new catalytic processes such as hydrogenation, oxidation and reduction reactions.</p>Formula:C13H9NO4Purity:Min. 95%Color and Shape:PowderMolecular weight:243.21 g/mol
