4-(3-Fluorophenoxy)benzylamine

Base Information

Chemical Name:4-(3-Fluorophenoxy)benzylamine
CAS No.:864263-03-6
Molecular Formula:C13H12FNO
Molecular Weight:217.243
Hs Code.:2922299090
European Community (EC) Number:961-648-6
Mol file:864263-03-6.mol

Synonyms:864263-03-6;4-(3-fluorophenoxy)benzylamine;1-[4-(3-fluorophenoxy)phenyl]methanamine;[4-(3-fluorophenoxy)phenyl]methanamine;(4-(3-Fluorophenoxy)phenyl)methanamine;SCHEMBL506288;4-(3-fluorophenyloxy)benzylamine;LIOGVDBYTRYBOL-UHFFFAOYSA-N;BBL040101;MFCD04971077;STK349851;AKOS000218176;SB79026;DB-294672;CS-0240749;EN300-229892

Suppliers and Price of 4-(3-Fluorophenoxy)benzylamine

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

Crysdot
(4-(3-Fluorophenoxy)phenyl)methanamine 97%
10g
$ 947.00

Crysdot
(4-(3-Fluorophenoxy)phenyl)methanamine 97%
5g
$ 569.00

American Custom Chemicals Corporation
1-[4-(3-FLUOROPHENOXY)PHENYL]METHANAMINE 95.00%
5MG
$ 504.09

AK Scientific
4-(3-Fluorophenoxy)benzylamine
10g
$ 2331.00

AK Scientific
4-(3-Fluorophenoxy)benzylamine
500mg
$ 437.00

Acrotein
4-(3-Fluorophenoxy)benzylamine 97%
0.5g
$ 165.00

Total 3 raw suppliers

Chemical Property of 4-(3-Fluorophenoxy)benzylamine

Chemical Property:

PSA：35.25000
LogP:3.77700
XLogP3:2.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:217.090292168
Heavy Atom Count:16
Complexity:204

Purity/Quality:

99% ^*data from raw suppliers

(4-(3-Fluorophenoxy)phenyl)methanamine 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC(=C1)F)OC2=CC=C(C=C2)CN

Technology Process of 4-(3-Fluorophenoxy)benzylamine

There total 5 articles about 4-(3-Fluorophenoxy)benzylamine 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%

: 864263-03-6
4-((3''-fluoro)phenoxy)benzylamine

Guidance literature:

Reference yield: 65.0%

: 877149-18-3
4-((3'-fluoro)phenoxy)benzonitrile

: 864263-03-6
4-((3''-fluoro)phenoxy)benzylamine

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 - 20 ℃;
DOI:10.1021/jm100185c

Reference yield:

: 459-57-4
4-fluorobenzaldehyde

: 864263-03-6
4-((3''-fluoro)phenoxy)benzylamine

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium carbonate / acetone / Reflux

2.1: sodium hydrogencarbonate; hydroxylamine hydrochloride / ethanol / Reflux

2.2: Reflux

With hydroxylamine hydrochloride; sodium hydrogencarbonate; potassium carbonate; In ethanol; acetone;
DOI:10.1021/acs.jafc.8b06195