151696-86-5

Basic information

• Product Name: 2-[(4-Methoxy-benzyl)-Methyl-aMino]-ethanol
• Synonyms: 2-[(4-Methoxy-benzyl)-Methyl-aMino]-ethanol
• CAS NO: 151696-86-5
• Molecular Formula: C₁₁H₁₇NO₂
• Molecular Weight: 195.25818
• Mol File: 151696-86-5.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-[(4-Methoxy-benzyl)-Methyl-aMino]-ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(4-Methoxy-benzyl)-Methyl-aMino]-ethanol(151696-86-5)
• EPA Substance Registry System: 2-[(4-Methoxy-benzyl)-Methyl-aMino]-ethanol(151696-86-5)

Safety Data

• Hazardous Substances Data: 151696-86-5(Hazardous Substances Data)

Upstream product

• 39931-25-4 2-(4-Methoxyphenyl)-3-methyloxazolidine 
• 110-82-7 cyclohexane 
• 71-43-2 benzene 
• 123-91-1 1,4-dioxane 
• 64-17-5 ethanol 
• 123-11-5 4-methoxy-benzaldehyde 

Downstream Products

• 159050-44-9 2-ethyl 2-diazoacetoacetate 
• 54527-70-7 2-[N-(4-methoxybenzyl)-N-methylamino]-ethyl acetoacetate 

Relevant articles and documents

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Reductive Cleavage of N-Substituted 2-Aryl-1,3-oxazolidines: Generation of α-Amino-Substituted Carbanions

The behavior of several N-substituted 2-aryl-1,3-oxazolidines has been investigated under conditions of electron transfer from alkali metals in aprotic solvents.The reduction led to the regioselective cleavage of the benzylic carbon-oxygen bond, with formation of the corresponding N-substituted benzylamino alcohols in good yields.Investigation of the mechanism of this reductive cleavage, with the aid of labeling experiments, showed the intermediate formation of α-tertiary amino-substituted carbanions.