
CAS 89399-21-3
:N-Hexyl-4-nitrobenzamide
Description:
N-Hexyl-4-nitrobenzamide is an organic compound characterized by its amide functional group, which is formed from the reaction of a carboxylic acid and an amine. This compound features a hexyl chain, providing hydrophobic characteristics, and a nitro group attached to a benzene ring, which contributes to its reactivity and potential applications in various chemical processes. The presence of the nitro group typically enhances the compound's electron-withdrawing properties, influencing its behavior in chemical reactions. N-Hexyl-4-nitrobenzamide is likely to be a solid at room temperature, with moderate solubility in organic solvents due to its hydrophobic hexyl chain. Its molecular structure suggests potential uses in pharmaceuticals, agrochemicals, or as an intermediate in organic synthesis. Safety data should be consulted for handling and storage, as compounds with nitro groups can exhibit varying degrees of toxicity and environmental impact. Overall, N-Hexyl-4-nitrobenzamide represents a versatile compound with significant implications in chemical research and industry.
Formula:C13H18N2O3
InChI:InChI=1S/C13H18N2O3/c1-2-3-4-5-10-14-13(16)11-6-8-12(9-7-11)15(17)18/h6-9H,2-5,10H2,1H3,(H,14,16)
InChI key:InChIKey=YIQCYVHPIUGJKJ-UHFFFAOYSA-N
SMILES:C(NCCCCCC)(=O)C1=CC=C(N(=O)=O)C=C1
Synonyms:- N-Hexyl-4-nitrobenzamide
- Benzamide, N-hexyl-4-nitro-
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