7352-03-6

Basic information

• Product Name: N-(Ethoxymethyl)-N-ethylethanamine
• Synonyms: N-(Ethoxymethyl)diethylamine;N-(Ethoxymethyl)-N-ethylethanamine
• CAS NO: 7352-03-6
• Molecular Formula: C₇H₁₇NO
• Molecular Weight: 131.216
• Mol File: 7352-03-6.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 136.5°Cat760mmHg
• Flash Point: 34.7°C
• Appearance: /
• Density: 0.832g/cm³
• Vapor Pressure: 7.34mmHg at 25°C
• Refractive Index: 1.42
• PKA: 8.61±0.25(Predicted)
• CAS DataBase Reference: N-(Ethoxymethyl)-N-ethylethanamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(Ethoxymethyl)-N-ethylethanamine(7352-03-6)
• EPA Substance Registry System: N-(Ethoxymethyl)-N-ethylethanamine(7352-03-6)

Safety Data

• Hazardous Substances Data: 7352-03-6(Hazardous Substances Data)

Usage

InChI:InChI=1/C7H17NO/c1-4-8(5-2)7-9-6-3/h4-7H2,1-3H3

Upstream product

• 3275-13-6 1-(ethoxymethyl)piperidine 
• 73477-65-3 diethyl-(octylmercapto-methyl)-amine 
• 50-00-0 formaldehyd 
• 109-89-7 diethylamine 
• 64-17-5 ethanol 

Downstream Products

• 5515-83-3 ethyl 3-(diethylamino)propionate 
• 27945-00-2 N,N-diethyl-β-diethylaminopropionic acid amide 
• 92321-70-5 diethyl-trans-cinnamyloxymethyl-amine 
• 67232-11-5 diethyl-benzyloxymethyl-amine 
• 6630-03-1 6-(N,N-diethylaminomethyl)-2,5-dimethylphenol 
• 69286-57-3 4-(N,N-diethylaminomethyl)-2,5-dimethylphenol 
• 120983-08-6 4,6-bis(N,N-diethylaminomethyl)-2,5-dimethylphenol 
• 22396-72-1 diethyl-(3-phenyl-prop-2-ynyl)-amine 
• 94-38-2 3-diethylamino-1-phenyl-propan-1-one 
• 37408-85-8 2-[(diethylamino)methyl]-cyclohexanone 
• 82343-79-1 2-(Diethylaminomethyl)cyclopentanon 
• 685-91-6 diethylacetamide 
• 1825-62-3 ethyl trimethylsilyl ether 
• 128429-58-3 5-<(diethylamino)methyl>-1,4,6,9-tetraoxa-5λ⁵-phosphaspiro<4.4>nonane 

Relevant articles and documents

The generation of iminium ions using chlorosilanes and their reactions with electron rich aromatic heterocycles

Dichlorodimethylsilane and trichloromethylsilane have been used to generate iminium ions from aminals and aminol ethers derived from secondary alkylamines, including glycine derivatives, in aprotic media which were shown to undergo reactions with electron rich aromatic heterocycles, including furan, to give mono-aminoalkylation products in good yields. Whereas chlorotrimethylsilane has been shown to generate iminium ions from aminol ethers, no evidence was adduced for the involvement of iminium ions using aminals. 2,5-Disubstitution of N-methylpyrrole was the major result in reactions of N-methylpyrrole with aminals in the presence of chlorotrimethylsilane where no build up of hydrogen chloride occurs and where chlorotrimethylsilane can function catalytically. Experimental results, including the use of bis(trimethylsilyl)acetamide as a proton scavenger, and some relative rate data, are presented that allow possible mechanisms to be evaluated.

A Convenient Synthesis of N,N-Disubstituted Aminomethyltri-n-butylstannanes, Precursors of the Corresponding Lithium Reagents

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