CAS 7022-47-1

2-Chloro-N-methyl-N-phenylbenzamide

Description:

2-Chloro-N-methyl-N-phenylbenzamide, with the CAS number 7022-47-1, is an organic compound characterized by its amide functional group, which is derived from benzoic acid. This compound features a chlorine atom attached to the second carbon of the benzene ring, along with a methyl and a phenyl group attached to the nitrogen atom of the amide. It typically appears as a solid or crystalline substance and is soluble in organic solvents. The presence of the chlorine atom contributes to its reactivity and potential applications in various chemical reactions, including nucleophilic substitutions. The compound may exhibit biological activity, making it of interest in pharmaceutical research. Its molecular structure allows for interactions with biological targets, which can be explored for therapeutic purposes. As with many chlorinated compounds, it is essential to handle it with care due to potential toxicity and environmental concerns. Proper safety measures should be observed when working with this substance in laboratory settings.

Formula: C₁₄H₁₂ClNO

InChI: InChI=1S/C14H12ClNO/c1-16(11-7-3-2-4-8-11)14(17)12-9-5-6-10-13(12)15/h2-10H,1H3

InChI key: InChIKey=OEYWSNRVIODBJL-UHFFFAOYSA-N

SMILES: C(N(C)C1=CC=CC=C1)(=O)C2=C(Cl)C=CC=C2

Synonyms:

• Benzamide, 2-chloro-N-methyl-N-phenyl-
• Benzanilide, 2-chloro-N-methyl-
• N-Methyl-N-phenyl-2-chlorobenzamide
• 2-Chloro-N-methyl-N-phenylbenzamide
• 2-Chloro-N-methylbenzanilide

(2-Chlorophenyl)-n-methyl-n-benzamide

CAS: 7022-47-1

2-Chlorophenyl-N-methyl-N-benzamide is a natural product that is structurally related to vasicine and iodides. It was synthesized by the catalytic reaction of an aryl chloride and an aryl bromide in the presence of copper(II) acetate. The bioactive synthetic products were obtained using a transition metal as the catalyst. The synthesis of 2-chlorophenyl-N-methyl-N-benzamide has been achieved by irradiation of chlorobenzene with ultraviolet light and then reacting it with ammonia in the presence of hydrogen peroxide. This process yielded 2,4,6,8,10,12,14,16 chlorinated derivatives which have been shown to be reactive with nucleophiles such as amines or thiols.

Formula: C₁₄H₁₂ClNO

Purity: Min. 95%

Color and Shape: Clear Liquid

Molecular weight: 245.7 g/mol

Ref: 3D-FC145672