2-Ethoxyethylamine

Base Information

• Chemical Name: 2-Ethoxyethylamine
• CAS No.: 110-76-9
• Molecular Formula: C4H11NO
• Molecular Weight: 89.1374
• Hs Code.: 2922199090
• European Community (EC) Number: 203-801-5
• DSSTox Substance ID: DTXSID8059392
• Nikkaji Number: J149.675A
• Wikidata: Q63392162
• Mol file: 110-76-9.mol

Synonyms:2-ethoxyethylamine

Chemical Property of 2-Ethoxyethylamine

Chemical Property:

• Vapor Pressure: 25.5mmHg at 25°C
• Refractive Index: 1.4080 to 1.4110
• Boiling Point: 108.8 °C at 760 mmHg
• PKA: pK1:6.26(+1) (25°C)
• Flash Point: 17.7 °C
• PSA: 35.25000
• Density: 0.852 g/cm³
• LogP: 0.68190
• Water Solubility.: Completely miscible in water
• XLogP3: -0.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 89.084063974
• Heavy Atom Count: 6
• Complexity: 23.5

Purity/Quality:

98% ^*data from raw suppliers

2-Ethoxyethylamine ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xn
• Hazard Codes: Xn
• Statements: 10-34-41-37/38-22
• Safety Statements: 26-36/37/39-39

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCOCCN

Technology Process of 2-Ethoxyethylamine

There total 14 articles about 2-Ethoxyethylamine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 18.0%

→ 4-[(2-ethoxy-ethylamino)-methyl]-N-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-benzamide + 2-ethoxy-1-ethanamine (110-76-9)

Guidance literature:

Reference yield:

1-nitro-2-ethoxyethane (31890-52-5) → 2-ethoxy-1-ethanamine (110-76-9)

Guidance literature:

With ethanol; platinum; at 20 ℃; under 73550.8 Torr; Hydrogenation;

Reference yield:

2-ethoxy-ethanol (110-80-5) → 2-ethoxy-1-ethanamine (110-76-9)

Guidance literature:

With copper chromite; ammonia; at 200 ℃;

upstream raw materials:

2-ethoxy-ethanol

2-ethoxyacetonitrile

1-nitro-2-ethoxyethane

sodium ethanolate

Downstream raw materials:

bis-(2-ethoxyethyl)amine

N-(2-ethoxy-ethyl)-2-hydroxy-benzamidine

6-Chloro-2-(2-ethoxy-ethylamino)-N-(2-methoxy-ethyl)-3-sulfamoyl-benzamide

6-Chloro-N-(2-diethylamino-ethyl)-2-(2-ethoxy-ethylamino)-3-sulfamoyl-benzamide

Refernces

• 1、 -. "HIV INTEGRASE INHIBITORS". . . Retrieved 2015/09/22.
• 2、 -. "2-aminobenzoxazole derivatives and combinatorial libraries thereof". . . Retrieved 2008/06/13.