7204-35-5

Basic information

• Product Name: Phenol, 2-[(dimethylamino)methyl]-4-methyl-
• CAS NO: 7204-35-5
• Molecular Formula: C10H15NO
• Molecular Weight: 165.235
• Mol File: 7204-35-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Phenol, 2-[(dimethylamino)methyl]-4-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 2-[(dimethylamino)methyl]-4-methyl-(7204-35-5)
• EPA Substance Registry System: Phenol, 2-[(dimethylamino)methyl]-4-methyl-(7204-35-5)

Safety Data

• Hazardous Substances Data: 7204-35-5(Hazardous Substances Data)

Upstream product

• 3534-33-6 3,4-dihydro-3,6-dimethyl-2H-1,3-benz[e]oxazine 
• 50-00-0 formaldehyd 
• 106-44-5 p-cresol 
• 64-17-5 ethanol 
• 7732-18-5 water 
• 124-40-3 dimethyl amine 
• 237431-65-1 4-Methyl-2-{[methyl-((R)-1-phenyl-ethyl)-amino]-methyl}-phenol 
• 237431-64-0 6-methyl-3-[(1R)-1-phenylethyl]3,4-dihydro-2H-1,3-benz[e]oxazine 
• 237431-66-2 2-hydroxy-5-methyl-N-methylbenzylamine 

Downstream Products

• 109044-10-2 dimethyl-carbamic acid-(2-dimethylaminomethyl-4-methyl-phenyl ester) 
• 75445-46-4 2-(2-Amino-2-methylpropyl)-4-methylphenol 
• 75445-40-8 4-Methyl-2-(2-methyl-2-nitropropyl)phenol 
• 731843-23-5 C₁₀H₁₄N₂O₃ 
• 21236-74-8 4-methyl-2-(piperidin-1-ylmethyl)phenol 
• 82807-53-2 4-methyl-2-(4-morpholinylmethyl)phenol 
• 67853-12-7 (2-hydroxy-5-methyl-benzyl)-trimethyl-ammonium; iodide 
• 569646-48-6 [2-(tert-butyl-diphenyl-silanyloxy)-5-methyl-benzyl]-dimethyl-amine 
• 74714-13-9 (4-Methoxy-phenyl)-(6-methyl-4H-chromen-3-yl)-methanone 
• 75637-70-6 2-(diphenylphosphinomethyl)-4-methylphenol 
• 64046-29-3 trimethyl-(5-methyl-2-methylcarbamoyloxy-benzyl)-ammonium; iodide 

Relevant articles and documents

Convenient synthesis of 2-Amino-4H-chromenes from photochemically generated o-quinone methides and malononitrile

2-Amino-4H-chromenes were synthesized in moderate to good yields by the reaction of o-quinone methides photochemically generated from o-(dimethylaminomethyl)phenols with malononitrile. This method was applicable to the synthesis of fluorinated chromenes that were difficult to obtain by other methods. In addition, o-(hydroxymethyl)phenols could be used for the reaction in the presence of tertiary amine bases.

The first enantioselective syntheses of axially chiral enantiomerically pure calix[4]resorcinarene derivatives [3]

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