CAS 3393-96-2
:N-(4-Nitrophenyl)benzamide
Description:
N-(4-Nitrophenyl)benzamide, with the CAS number 3393-96-2, is an organic compound characterized by its amide functional group and the presence of a nitrophenyl substituent. This compound features a benzamide structure where a nitro group is attached to the para position of the phenyl ring. It typically appears as a solid at room temperature and is known for its yellow color due to the nitro group. The presence of the nitro group contributes to its electron-withdrawing properties, which can influence its reactivity and solubility in various solvents. N-(4-Nitrophenyl)benzamide is often utilized in organic synthesis and can serve as an intermediate in the production of dyes, pharmaceuticals, and other chemical compounds. Its properties, such as melting point, boiling point, and solubility, can vary depending on the specific conditions and purity of the sample. Safety precautions should be taken when handling this compound, as nitro compounds can be hazardous.
Formula:C13H10N2O3
InChI:InChI=1S/C13H10N2O3/c16-13(10-4-2-1-3-5-10)14-11-6-8-12(9-7-11)15(17)18/h1-9H,(H,14,16)
InChI key:InChIKey=GMGQGZYFQSCZCW-UHFFFAOYSA-N
SMILES:C(NC1=CC=C(N(=O)=O)C=C1)(=O)C2=CC=CC=C2
Synonyms:- 222-241-2
- 4′-Nitrobenzanilide
- Benzamide, N-(4-nitrophenyl)-
- Benzanilide, 4′-nitro-
- N-(4-Nitrophenyl)benzamide
- N-(p-Nitrophenyl)benzamide
- N-Benzoyl-4-nitroaniline
- N-Benzoyl-p-nitroaniline
- NSC 82120
- p-Nitro-N-benzoylaniline
- p′-Nitrobenzanilide
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Found 5 products.
4'-Nitrobenzanilide
CAS:Formula:C13H10N2O3Purity:>98.0%(GC)Color and Shape:White to Orange to Green powder to crystalMolecular weight:242.234'-Nitrobenzanilide
CAS:<p>4'-Nitrobenzanilide</p>Formula:C13H10N2O3Purity:98%Color and Shape: gray solidMolecular weight:242.23g/mol4'-Nitrobenzanilide
CAS:<p>4'-Nitrobenzanilide is an organic compound that is used to synthesize dyes and other chemicals. It can be prepared by reacting a primary or secondary amine with 4-nitrochlorobenzene in the presence of a base. This reaction produces the nitroanilide, which can be oxidized to the nitrobenzanilide. The high yield and low toxicity of this process make it an attractive alternative to older methods of production. 4'-Nitrobenzanilide has been shown to have significant environmental effects, particularly in terms of pollution caused by chlorinated solvents.</p>Formula:C13H10N2O3Purity:Min. 95%Molecular weight:242.23 g/mol




