N-Benzyl-2-morpholinoethanamine

Base Information

Chemical Name:N-Benzyl-2-morpholinoethanamine
CAS No.:2038-05-3
Molecular Formula:C13H20N2O
Molecular Weight:220.315
Hs Code.:
DSSTox Substance ID:DTXSID40405954
Nikkaji Number:J1.165.317K
Wikidata:Q82210739

Synonyms:N-Benzyl-2-morpholinoethanamine;2038-05-3;N-benzyl-2-morpholin-4-ylethanamine;benzyl[2-(morpholin-4-yl)ethyl]amine;4-Morpholineethanamine, N-(phenylmethyl)-;N-benzyl-2-morpholinoethan-1-amine;N-benzyl-N-[2-(4-morpholinyl)ethyl]amine;SCHEMBL39631;DTXSID40405954;MSFAUJOUPQMLNF-UHFFFAOYSA-N;AKOS000238303;AS-64874;CS-0156267;D70722;EN300-192665;AN-465/10819004

Suppliers and Price of N-Benzyl-2-morpholinoethanamine

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

Total 6 raw suppliers

Chemical Property of N-Benzyl-2-morpholinoethanamine

Chemical Property:

XLogP3:1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:220.157563266
Heavy Atom Count:16
Complexity:175

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1COCCN1CCNCC2=CC=CC=C2

Technology Process of N-Benzyl-2-morpholinoethanamine

There total 5 articles about N-Benzyl-2-morpholinoethanamine 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: 100.0%

: 2-fluoro-N-(2-morpholin-4-yl-ethyl)-benzamide

: 2038-05-3
4-(N-benzyl-2-aminoethyl)morpholine

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; at 65 ℃; for 8h;
DOI:10.1016/S0040-4039(99)01397-0

Reference yield: 66.0%

: 2038-03-1
4-(2-AMINOETHYL)MORPHOLINE

: 100-46-9
benzylamine

: 2038-05-3
4-(N-benzyl-2-aminoethyl)morpholine

: 103-49-1
dibenzylamine

Guidance literature:: With 1-(3-amino-2,4-dihydroxyphenyl)-1-ethanone; In methanol; at 20 ℃; for 4h; chemoselective reaction; Inert atmosphere; Electrochemical reaction;
DOI:10.1021/ol802885b

Reference yield:

: 5807-02-3
4-morpholinoacetonitrile

: 2038-05-3
4-(N-benzyl-2-aminoethyl)morpholine

Guidance literature:: Multi-step reaction with 3 steps

1: Raney nickel; methanol. NH₃ / Hydrogenation

2: unter Entfernen des entstehenden H₂O

3: platinum; methanol / Hydrogenation

With methanol; ammonia; nickel; platinum;
DOI:10.1002/ardp.19582910303