2-Chloro-2’,6’-dimethylacetanilide

• CAT Number: R050680
• CAS Number: 1131-01-7
• Molecular Formula: C10H12ClNO
• Molecular Weight: 197.662
• Purity: ≥95%
• Synonyms: 2-Chloro-N-(2,6-dimethylphenyl)acetamide; 1-Chloroacetylamino-2,6-dimethylbenzene; 2-Chloro-2’,6’-acetoxylidide; 2’,6’-Dimethyl-2-chloroacetanilide; Chloroacetamido-2,6-xylidine; Chloroaceto-2,6-xylidide; N-(2,6-Dimethylphenyl)-2-chloroacetamide; N-(
• Storage: -20°C
• IUPAC Name: 2-chloro-N-(2,6-dimethylphenyl)acetamide
• InChI: InChI=1S/C10H12ClNO/c1-7-4-3-5-8(2)10(7)12-9(13)6-11/h3-5H,6H2,1-2H3,(H,12,13)
• InChIKey: FPQQSNUTBWFFLB-UHFFFAOYSA-N
• SMILES: CC1=C(C(=CC=C1)C)NC(=O)CCl

2-Chloro-2′,6′-dimethylacetanilide (Cat No.:R050680) is also known as 2-chloro-N-(2,6-dimethylphenyl)acetamide; 1-Chloroacetamido-2,6-dimethylbenzene, commonly used in pharmaceutical intermediates.

Reference

1.Riise Moen, Anders, Rasmus Karstad, and Thorleif Anthonsen. "Chemo-enzymatic synthesis of both enantiomers of the anti-anginal drug ranolazine." Biocatalysis and Biotransformation 23.1 (2005): 45-51.
2.Yogeeswari, Perumal, et al. "Synthesis and anticonvulsant activity of 4-(2-(2, 6-dimethylphenylamino)-2-oxoethylamino)-N-(substituted) butanamides: A pharmacophoric hybrid approach." Bioorganic & medicinal chemistry letters 17.13 (2007): 3712-3715.