39667-14-6

Basic information

• Product Name: 2,6-dimethoxy-4-phenol
• Synonyms: 2,6-dimethoxy-4-phenol;Phenol, 4-[(dimethylamino)methyl]-2,6-dimethoxy-
• CAS NO: 39667-14-6
• Molecular Formula: C₁₁H₁₇NO₃
• Molecular Weight: 211.25758
• Mol File: 39667-14-6.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,6-dimethoxy-4-phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-dimethoxy-4-phenol(39667-14-6)
• EPA Substance Registry System: 2,6-dimethoxy-4-phenol(39667-14-6)

Safety Data

• Hazardous Substances Data: 39667-14-6(Hazardous Substances Data)

Upstream product

• 50-00-0 formaldehyd 
• 530-57-4 3,5-dimethoxy-4-hydroxybenzoic acid 
• 124-40-3 dimethyl amine 
• 91-10-1 1,3-dimethoxy-2-hydroxy-benzene 
• 68-12-2 N,N-dimethyl-formamide 
• 134-96-3 syringic aldehyde 

Downstream Products

• 21253-61-2 2,6-Dimethoxy-4-(2,4,6-triamino-pyrimidin-5-ylmethyl)-phenol 
• 73576-14-4 4-(2,4-Diamino-6-methoxy-pyrimidin-5-ylmethyl)-2,6-dimethoxy-phenol 
• 39667-15-7 4-(2,4-Diamino-6-methylsulfanyl-pyrimidin-5-ylmethyl)-2,6-dimethoxy-phenol 
• 15640-40-1 bis(4-hydroxy-2,6-dimethoxyphenyl)methane 
• 21253-58-7 2,4-diamino-5-(3,5-dimethoxy-4-hydroxybenzyl)pyrimidine 
• 72380-55-3 trimethyl(3,5-dimethoxy-4-hydroxybenzyl)ammonium iodide salt 
• 4385-56-2 2-(4-hydroxy-3,5-dimethoxyphenyl)acetic acid 
• 2413-00-5 2-(4-Hydroxy-3,5-dimethoxyphenyl)ethanamin 
• 13338-63-1 2-(3,4,5-trimethoxyphenyl)acetonitrile 
• 54-04-6 mescaline 
• 115319-96-5 6-<(dimethylamino)methyl>-3-hydroxy-2,4-dimethoxy-5-(methylthio)-α-phenylbenzyl alcohol 
• 115319-95-4 5-deuterio-4-<(dimethylamino)methyl>-2,6-dimethoxy-3-(methylthio)phenol 
• 115319-94-3 4-<(dimethylamino)methyl>-2,6-dimethoxy-3,5-bis(methylthio)phenol 
• 115320-03-1 2,6-dimethoxy-3,5-bis(methylthio)-1,4-benzoquinone 

Relevant articles and documents

The sustainable heterogeneous catalytic reductive amination of lignin models to produce aromatic tertiary amines

A novel heterogeneous catalytic process for efficient reductive amination is developed in the presence of heterogeneous zirconium-based catalysts, in which N,N-dimethylformamide is used as the solvent, low-molecular-weight amine source and reductant. Aromatic tertiary amines have been produced from lignin-derived aromatic aldehydes via the mild Leuckart reaction with ZrO2 or ZrO(OH)2 as catalysts, for instance, a 95.8% yield of N,N-dimethyl-1-(3,4,5-trimethoxyphenyl)methanamine in a 100% selectivity is obtained from the reductive amination of 3,4,5-trimethoxybenzaldehyde under mild conditions.

Benzylamine Antioxidants: Relationship between Structure, Peroxyl Radical Scavenging, Lipid Peroxidation Inhibition, and Cytoprotection

Three homologous series of 3,5-dialkoxy-4-hydroxybenzylamines were prepared and tested (1) as peroxyl radical scavengers in homogeneous aqueous solution, (2) as inhibitors of iron-dependent peroxidation of rabbit brain vesicular membrane lipids, and (3) a

A novel route for the synthesis of mescaline

A new plausible synthetic pathway for the synthesis of the peyote alkaloid mescaline in a satisfactory overall yield is reported.