CAS 19313-87-2
:3-Chloro-N-(4-Methoxyphenyl)Propanamide
Description:
3-Chloro-N-(4-Methoxyphenyl)Propanamide is an organic compound characterized by its amide functional group, which is derived from propanoic acid. The presence of a chlorine atom at the third carbon position and a methoxy-substituted phenyl group at the nitrogen atom contributes to its unique chemical properties. This compound typically appears as a solid or crystalline substance and is soluble in organic solvents, reflecting its hydrophobic characteristics due to the aromatic methoxy group. The chlorine substituent can influence the compound's reactivity and polarity, making it potentially useful in various chemical reactions, including nucleophilic substitutions. Additionally, the methoxy group can enhance the compound's lipophilicity, which may affect its biological activity and interactions with other molecules. As with many amides, it may exhibit hydrogen bonding capabilities, influencing its physical properties such as melting point and boiling point. Overall, 3-Chloro-N-(4-Methoxyphenyl)Propanamide is of interest in medicinal chemistry and material science due to its structural features and potential applications.
Formula:C10H12ClNO2
InChI:InChI=1/C10H12ClNO2/c1-14-9-4-2-8(3-5-9)12-10(13)6-7-11/h2-5H,6-7H2,1H3,(H,12,13)
SMILES:COc1ccc(cc1)NC(=O)CCCl
Synonyms:- Salor-Int L254983-1Ea
- Propanamide, 3-Chloro-N-(4-Methoxyphenyl)-
- N-3-Chloropropionyl-(4-Methoxy)-Aniline
- Akos Bbs-00003931
- N-3-Chloroproiony-(4-Methoxy)-Aniline
- 3-Chloro-N-(4-Methoxyphenyl)Propionamide
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Found 5 products.
3-Chloro-N-(4-methoxyphenyl)propanamide
CAS:Formula:C10H12ClNO2Purity:97%Color and Shape:SolidMolecular weight:213.66083-Chloro-N-(4-methoxyphenyl)propanamide
CAS:3-Chloro-N-(4-methoxyphenyl)propanamidePurity:97%Molecular weight:213.66g/mol3-Chloro-N-(4-methoxyphenyl)propanamide
CAS:<p>3-Chloro-N-(4-methoxyphenyl)propanamide (PCMP) is a ligand that binds to aromatic systems. PCMP has been shown to react with alkylating agents, such as methyl iodide and dimethyl sulfate, to form a tetradentate ligand with two chloro groups and two methoxy groups. This compound can be used as a counterion for dianionic complexes, or it can be used for the synthesis of amides by deprotonation followed by intramolecular reaction.</p>Formula:C10H12ClNO2Purity:Min. 95%Molecular weight:213.66 g/mol





