53984-98-8

Basic information

• Product Name: 2-CYANO-N-(2,6-DIMETHYL-PHENYL)-ACETAMIDE
• Synonyms: Albb-008584;2-cyano-N-(2,6-dimethylphenyl)ethanamide;Acetamide, 2-cyano-N-(2,6-dimethylphenyl)-
• CAS NO: 53984-98-8
• Molecular Formula: C₁₁H₁₂N₂O
• Molecular Weight: 188.23
• Mol File: 53984-98-8.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 365.2 °C at 760 mmHg
• Flash Point: 174.7 °C
• Appearance: /
• Density: 1.141 g/cm³
• Vapor Pressure: 1.6E-05mmHg at 25°C
• Refractive Index: 1.577
• CAS DataBase Reference: 2-CYANO-N-(2,6-DIMETHYL-PHENYL)-ACETAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-CYANO-N-(2,6-DIMETHYL-PHENYL)-ACETAMIDE(53984-98-8)
• EPA Substance Registry System: 2-CYANO-N-(2,6-DIMETHYL-PHENYL)-ACETAMIDE(53984-98-8)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 53984-98-8(Hazardous Substances Data)

Usage

General Description

2-CYANO-N-(2,6-DIMETHYL-PHENYL)-ACETAMIDE is a chemical compound with the molecular formula C13H14N2O. It is a white to light brown powder with a molecular weight of 214.3 g/mol. 2-CYANO-N-(2,6-DIMETHYL-PHENYL)-ACETAMIDE is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It has also shown potential as an anticonvulsant and analgesic agent in pre-clinical studies. Additionally, studies have indicated that 2-CYANO-N-(2,6-DIMETHYL-PHENYL)-ACETAMIDE may have potential therapeutic effects in the treatment of neurodegenerative diseases. Overall, this chemical compound has shown promise in various research and development applications within the pharmaceutical and agrochemical industries.

InChI:InChI=1/C11H12N2O/c1-8-4-3-5-9(2)11(8)13-10(14)6-7-12/h3-5H,6H2,1-2H3,(H,13,14)

Upstream product

• 32433-61-7 2-bromo-N-(2,6-dimethyl-phenyl)-acetamide 
• 151-50-8 potassium cyanide 
• 87-62-7 2,6-dimethylaniline 
• 105-34-0 methyl 2-cyanoacetate 
• 16130-58-8 cyanoacetic acid chloride 
• 372-09-8 cyanoacetic acid 

Downstream Products

• 146494-83-9 2-Amino-4-(2,6-dimethyl-phenyl)-3-oxo-1,4-diaza-spiro[4.5]decane-2-carboxylic acid amide 
• 133550-51-3 AG 531 
• 512173-12-5 2-amino-3-{[(2,6-dimethylphenyl)amino]carbonyl}-1,8-naphthyridine 
• 512173-15-8 3-{[(2,6-dimethylphenyl)amino]carbonyl}-2-[(ethoxycarbonyl)amino]-1,8-naphthyridine 
• 138574-70-6 4-(2,6-Dimethyl-phenyl)-3-oxo-1,4-diaza-spiro[4.5]dec-1-ene-2-carboxylic acid amide 
• 1370047-82-7 N-(2,6-dimethylphenyl)-2,5-dihydro-2-imino-4,5,5-trimethylfuran-3-carboxamide 
• 1370047-84-9 N-(2,6-dimethylphenyl)-2-imino-4-methyl-1-oxaspiro[4.5]dec-3-ene-3-carboxamide 
• 1370047-85-0 N-(2,6-dimethylphenyl)-2,5-dihydro-4,5,5-trimethyl-2-oxofuran-3-carboxamide 
• 1370047-87-2 N-(2,6-dimethylphenyl)-4-methyl-2-oxo-1-oxaspiro[4.5]dec-3-ene-3-carboxamide 
• 1370047-90-7 N-(2,6-dimethylphenyl)-2,5-dihydro-2-imino-4,5,5-trimethylfuran-3-carboxamide hydrochloride 
• 1370047-92-9 N-(2,6-dimethylphenyl)-2-imino-4-methyl-1-oxaspiro[4.5]dec-3-ene-3-carboxamide hydrochloride 
• 951900-54-2 5-amino-N-(2,6-dimethylphenyl)-1-(4-fluorophenyl)-1H-1,2,3-triazole-4-carboxamide 

Relevant articles and documents

ATP competitive inhibitors of d-alanine-d-alanine ligase based on protein kinase inhibitor scaffolds

d-Alanine-d-alanine ligase (DDl) is an essential enzyme in bacterial cell wall biosynthesis and an important target for developing new antibiotics. Here, we describe a new approach to identify new inhibitor scaffolds for DDl based on similarity in the ATP

Alternating copolymerization of cyclohexene oxide and CO2 catalyzed by zinc complexes with new 3-amino-2-cyanoimidoacrylate ligands

New 3-amino-2-cyanoimidoacrylate ligands with varying steric demands have been synthesized. Zinc acetate complexes of these ligands catalyze the copolymerisation of CO2 and cyclohexene oxide, showing high activities (TOF up to over 200 h -1).