19861-69-9

Basic information

• Product Name: Phenol, 4-[(dimethylamino)methyl]-2-methoxy-
• CAS NO: 19861-69-9
• Molecular Formula: C10H15NO2
• Molecular Weight: 181.235
• Mol File: 19861-69-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Phenol, 4-[(dimethylamino)methyl]-2-methoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 4-[(dimethylamino)methyl]-2-methoxy-(19861-69-9)
• EPA Substance Registry System: Phenol, 4-[(dimethylamino)methyl]-2-methoxy-(19861-69-9)

Safety Data

• Hazardous Substances Data: 19861-69-9(Hazardous Substances Data)

Upstream product

• 121-33-5 vanillin 
• 68-12-2 N,N-dimethyl-formamide 
• 124-40-3 dimethyl amine 

Downstream Products

• 100-02-7 4-nitro-phenol 
• 498-00-0 4-hydroxymethyl-2-methoxyphenol 
• 109162-32-5 2-methoxy-4-(piperidin-1-ylmethyl)phenol 
• 115062-93-6 1-(4-hydroxy-3-methoxybenzyl)piperdin-1-ium chloride 
• 125660-98-2 4-((benzyloxy)methyl)-2-methoxyphenol 
• 498577-19-8 2-methoxy-4-(pyrrolidin-1-ylmethyl)phenol 
• 115319-81-8 2-methoxy-5-(methylthio)-3-(phenylthio)-1,4-benzoquinone 
• 115319-80-7 2-Methoxy-3-phenylsulfanyl-[1,4]benzoquinone 
• 112520-80-6 3-(methylthio)-2-methoxy-1,4-benzoquinone 
• 109685-10-1 3-deuterio-2-methoxy-1,4-benzoquinone 
• 80464-91-1 2-methoxy-5-(3'-methyl-2'-butenyl)-1,4-benzoquinone 
• 127757-17-9 5-(3'-hydroxy-3'-methylbutenyl)-2-methoxy-4-<(dimethylamino)methyl>phenol 
• 127757-24-8 2-methoxy-5-(3'-methyl-2'-butenyl)-4-<(dimethylamino)methyl>phenol 
• 115319-89-6 4-<(dimethylamino)methyl>-2-methoxy-3-(phenylthio)phenol 

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.