42266-03-5

Basic information

• Product Name: 3,5-dichloro-N-methylaniline
• Synonyms: 3,5-dichloro-N-methylaniline
• CAS NO: 42266-03-5
• Molecular Formula: C₇H₇Cl₂N
• Molecular Weight: 176.04318
• Mol File: 42266-03-5.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3,5-dichloro-N-methylaniline(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-dichloro-N-methylaniline(42266-03-5)
• EPA Substance Registry System: 3,5-dichloro-N-methylaniline(42266-03-5)

Safety Data

• Hazardous Substances Data: 42266-03-5(Hazardous Substances Data)

Upstream product

• 626-43-7 3,5-Dichloroaniline 
• 31592-84-4 N-(3,5-dichlorophenyl)-acetamide 

Downstream Products

• 1427462-03-0 5-(((3,5-dichlorophenyl)(methyl)amino)methyl)-1-methyl-2-vinyl-1H-pyrazol-3(2H)-one 
• 1427462-02-9 3,5-dichloro-N-((2,3-dihydropyrazolo[5,1-b]oxazol-6-yl)methyl)-N-methylaniline 
• 1427462-01-8 C₂₀H₂₁Cl₂N₃O₄S 
• 1427461-95-7 C₁₈H₁₇Cl₂N₃O 
• 1427461-97-9 C₁₂H₁₃Cl₂N₃O 

Relevant articles and documents

Expedient stereospecific Co-catalyzed tandem C-N and C-O bond formation of: N -methylanilines with styrene oxides

Cobalt(ii)-catalyzed stereospecific coupling of N-methylanilines with styrene oxides is developed via tandem C-N and C-O bond formation using tert-butyl hydroperoxide (TBHP) as an oxidant. Optically active epoxide can be reacted with high optical purity.

Kynurenic Acid Derivatives. Structure-Activity Relationships for Excitatory Amino Acid Antagonism and Identification of Potent and Selective Antagonists at the Glycine Site of the N-Methyl-D-aspartate Receptor

Derivatives of the nonselective excitatory amino acid antagonist kynurenic acid (4-oxo-1,4-dihydroquinoline-2-carboxylic acid, 1) have been synthesized and evaluated for in vitro antagonist activity at the excitatory amino acid receptors sensitive to N-me