7179-86-4

Basic information

• Product Name: N-ethyltetrahydrofurfurylamine
• Synonyms: N-ethyltetrahydrofurfurylamine;N-Ethyltetrahydro-2-furanmethanamine;N-(tetrahydrofuran-2-ylmethyl)ethanamine(SALTDATA: FREE);N-(tetrahydrofuran-2-ylmethyl)ethanamine;N-(tetrahydro-2-furanylmethyl)ethanamine
• CAS NO: 7179-86-4
• Molecular Formula: C₇H₁₅NO
• Molecular Weight: 129.2001
• EINECS: 230-543-0
• Mol File: 7179-86-4.mol

Chemical Properties

• Boiling Point: 177.4°C at 760 mmHg
• Flash Point: 64.1°C
• Appearance: /
• Density: 0.905g/cm³
• Vapor Pressure: 1.04mmHg at 25°C
• Refractive Index: 1.44
• PKA: 9.74±0.10(Predicted)
• CAS DataBase Reference: N-ethyltetrahydrofurfurylamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-ethyltetrahydrofurfurylamine(7179-86-4)
• EPA Substance Registry System: N-ethyltetrahydrofurfurylamine(7179-86-4)

Safety Data

• Hazardous Substances Data: 7179-86-4(Hazardous Substances Data)

Usage

Uses

Used in Polymer and Resin Production:
N-ethyltetrahydrofurfurylamine is used as a solvent and stabilizer in the production of polymers and resins, contributing to the formation of high-quality materials with enhanced stability and performance.
Used in Pharmaceutical Manufacturing:
In the pharmaceutical industry, N-ethyltetrahydrofurfurylamine is utilized as a solvent and stabilizer for the production of various medications, ensuring the quality and efficacy of the final products.
Used in Agricultural Product Manufacturing:
N-ethyltetrahydrofurfurylamine is employed in the manufacturing of agricultural products, serving as a solvent and stabilizer to improve the performance and shelf life of these products.
Used in Industrial and Commercial Applications:
Due to its versatile properties as a solvent and stabilizer, N-ethyltetrahydrofurfurylamine is widely used in a range of industrial and commercial applications, providing solutions for various processes and products.

InChI:InChI=1/C7H15NO/c1-2-8-6-7-4-3-5-9-7/h7-8H,2-6H2,1H3

Upstream product

• 3003-84-7 Tetrahydrofurfuryl chloride 
• 75-04-7 ethylamine 
• 98-01-1 furfural 
• 97-99-4 Tetrahydrofurfuryl alcohol 
• 75-05-8 acetonitrile 

Downstream Products

• 856698-74-3 N²-(2-bromo-4-isopropyl-phenyl)-N⁴-ethyl-6-methyl-3-nitro-N⁴-(tetrahydro-furan-2-ylmethyl)-pyridine-2,4-diamine 
• 856684-32-7 ((2-bromo-4-isopropyl-phenyl)-{4-[ethyl-(tetrahydro-furan-2-ylmethyl)-amino]-6-methyl-3-nitro-pyridin-2-yl}-amino)-acetic acid ethyl ester 
• 1226889-02-6 tert-butyl 4-(ethyl((tetrahydrofuran-2-yl)methyl)amino)-2-(4-(2-methyl-1H-imidazol-1-yl)phenylamino)-7,8-dihydropyrido[4,3-d]pyrimidine-6(5H)-carboxylate 
• 1226889-20-8 tert-butyl 4-(ethyl((tetrahydrofuran-2-yl)methyl)amino)-2-(4-(oxazol-5-yl)phenylamino)-7,8-dihydropyrido[4,3-d]pyrimidine-6(5H)-carboxylate 

Relevant articles and documents

COUMARAN GROUP CONTAINING AMINE COMPOUNDS AND THEIR ACID ADDITION SALTS AND QUATERNARY AMMONIUM SALTS AND THE USE THEREOF AS ANTI ARRHYTHMIC AGENTS AND AS PSYCHOTROPIC AGENTS

Amine represented by the following formula (1), or their acid addition salts or their quaternary ammonium salts. STR1 The amines of formula (1) or their pharmaceutically acceptable acid addition salts or quaternary ammonium salts are useful for the treatment and prevention of heart diseases of animals, particularly arrhythima, myocardial infarction, angina pectoris and heart failure and psychoneurological diseases.

Catalytic Hydroamination of Furfuryl and Tetrahydrofurfuryl Alcohols with Nitriles

Reaction of furfuryl and tetrahydrofurfuryl alcohols with nitriles over copper oxide catalysts under a hydrogen pressure of 15 atm at a temperature of 230 deg C gives N-alkylfurfuryl- (yield 46-50percent) and N-alkyltetrahydrofurfurylamines (49-53percent), and N-alkylpiperidines (28-41percent).A reaction mechanism is proposed.