5-[ethyl(2-hydroxyethyl)amino]pentan-2-one

Base Information

Chemical Name:5-[ethyl(2-hydroxyethyl)amino]pentan-2-one
CAS No.:74509-79-8
Molecular Formula:C9H19 N O2
Molecular Weight:173.255
Hs Code.:2922509090
European Community (EC) Number:277-901-2
UNII:2H7VFB9CRN
DSSTox Substance ID:DTXSID00996015
Nikkaji Number:J349.415B
Wikidata:Q82987659
Mol file:74509-79-8.mol

Synonyms:5-[N-Ethyl-N-(2-hydroxyethyl)amino]-2-pentanone

Suppliers and Price of 5-[ethyl(2-hydroxyethyl)amino]pentan-2-one

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

AK Scientific
5-[Ethyl(2-hydroxyethyl)amino]pentan-2-one
5g
$ 1396.00

Total 29 raw suppliers

Chemical Property of 5-[ethyl(2-hydroxyethyl)amino]pentan-2-one

Chemical Property:

Vapor Pressure:0.000401mmHg at 25°C
Boiling Point:282.2°C at 760 mmHg
Flash Point:124.5°C
PSA：40.54000
Density:0.968g/cm³
LogP:0.66980
XLogP3:0
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:7
Exact Mass:173.141578849
Heavy Atom Count:12
Complexity:126

Purity/Quality:

99.9% ^*data from raw suppliers

5-[Ethyl(2-hydroxyethyl)amino]pentan-2-one ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCN(CCCC(=O)C)CCO
Uses 5-[ethyl(2-hydroxyethyl)amino]pentan-2-one can be used as organic synthesis intermediate and pharmaceutical intermediate, mainly used in laboratory research and development process and chemical production process.

Technology Process of 5-[ethyl(2-hydroxyethyl)amino]pentan-2-one

There total 4 articles about 5-[ethyl(2-hydroxyethyl)amino]pentan-2-one 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: 94.7%

: 5891-21-4
5-chloro-2-pentanone

: 110-73-6
2-(Ethylamino)ethanol

: 74509-79-8
5-(N-ethyl-N-2-hydroxyethylamine)-2-pentanone

Guidance literature:: With tetrabutylammomium bromide; potassium hydroxide; In chloroform; water; at 20 - 30 ℃; for 3h;

Reference yield: 86.0%

: 3695-29-2
5-iodo-2-pentanone

: 110-73-6
2-(Ethylamino)ethanol

: 74509-79-8
5-(N-ethyl-N-2-hydroxyethylamine)-2-pentanone

Guidance literature:: With potassium carbonate; In tetrahydrofuran; at 80 - 100 ℃; for 0.166667h; Flow reactor; Inert atmosphere;
DOI:10.3762/bjoc.14.45

Reference yield:

: 517-23-7,594837-91-9,98634-97-0,313643-49-1
3-acetyl-2-oxo-4,5-dihydrofuran

: 74509-79-8
5-(N-ethyl-N-2-hydroxyethylamine)-2-pentanone

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogen iodide / water / 0.08 h / 80 °C / 2250.23 Torr / Inert atmosphere; Flow reactor

2: potassium carbonate / tetrahydrofuran / 0.17 h / 80 - 100 °C / Flow reactor; Inert atmosphere

With hydrogen iodide; potassium carbonate; In tetrahydrofuran; water;
DOI:10.3762/bjoc.14.45