CAS 582-78-5
:N-(4-Methylphenyl)benzamide
Description:
N-(4-Methylphenyl)benzamide, also known as p-tolylbenzamide, is an organic compound characterized by its amide functional group attached to a benzene ring substituted with a para-methyl group. This compound typically appears as a white to off-white crystalline solid. It has a relatively high melting point, indicative of strong intermolecular interactions, such as hydrogen bonding, due to the presence of the amide group. The molecular structure features a phenyl ring and a methyl group, contributing to its hydrophobic characteristics. N-(4-Methylphenyl)benzamide is soluble in organic solvents like ethanol and acetone but has limited solubility in water, reflecting its non-polar nature. It is often used in organic synthesis and may serve as an intermediate in the production of pharmaceuticals or agrochemicals. Additionally, the compound's properties can be influenced by its molecular interactions, making it of interest in studies related to drug design and material science. Safety data should be consulted for handling and exposure guidelines, as with any chemical substance.
Formula:C14H13NO
InChI:InChI=1S/C14H13NO/c1-11-7-9-13(10-8-11)15-14(16)12-5-3-2-4-6-12/h2-10H,1H3,(H,15,16)
InChI key:InChIKey=YUIHXKGKVSVIEL-UHFFFAOYSA-N
SMILES:C(NC1=CC=C(C)C=C1)(=O)C2=CC=CC=C2
Synonyms:- 4-Phenyl-N-methylbenzamide
- Ai3-00503
- Benzamide, N-(4-methylphenyl)-
- Benzoic acid p-toluidide
- N-(4-Tolyl)benzamide
- N-(4-methylphenyl)benzamide
- N-(p-Methylphenyl)benzamide
- N-Benzoyl-4-methylaniline
- N-Benzoyl-p-toluidine
- N-p-Tolylbenzamide
- NSC 17586
- p-Benzotoluidide
- See more synonyms
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Found 5 products.
N-(4-methylphenyl)benzamide
CAS:Formula:C14H13NOPurity:%Color and Shape:SolidMolecular weight:211.2591N-(4-Methylphenyl) Benzamide
CAS:Controlled ProductFormula:C14H13NOColor and Shape:NeatMolecular weight:211.259N-(4-Methylphenyl)benzamide
CAS:<p>N-(4-Methylphenyl)benzamide (NMPBA) is a hydroxide ion-based reagent that can be used for the synthesis of carbonyl compounds. It has been shown to react with carbonyl compounds under mild conditions, forming an amide and a mixture of alcoholysis products. NMPBA is also capable of eliminating sulfides and thiols as well as reducing aromatic rings. The elimination reactions are optimized by irradiation and the structure-activity relationships have been investigated by organic chemistry experiments.</p>Formula:C14H13NOPurity:Min. 95%Molecular weight:211.26 g/mol




