1-[4-(2-Fluorophenoxy)phenyl]methanamine

Base Information

Chemical Name:1-[4-(2-Fluorophenoxy)phenyl]methanamine
CAS No.:864263-02-5
Molecular Formula:C₁₃H₁₂FNO
Molecular Weight:217.243
Hs Code.:
DSSTox Substance ID:DTXSID101285256
Mol file:864263-02-5.mol

Synonyms:864263-02-5;1-[4-(2-fluorophenoxy)phenyl]methanamine;(4-(2-Fluorophenoxy)phenyl)methanamine;4-(2-fluorophenoxy)benzylamine;[4-(2-fluorophenoxy)phenyl]methanamine;SCHEMBL507282;4-(2-Fluorophenoxy)benzyl amine;4-(2-fluorophenyloxy)benzylamine;QYXCKJOXQGBFIV-UHFFFAOYSA-N;4-(2'-Fluorophenoxy)-benzylamine;DTXSID101285256;MFCD04971076;STK349850;4-(2-Fluorophenoxy)benzenemethanamine;AKOS000218028;SB78805;BS-53208;DB-179230;CS-0226778;E84724;EN300-229891

Suppliers and Price of 1-[4-(2-Fluorophenoxy)phenyl]methanamine

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

American Custom Chemicals Corporation
1-[4-(2-FLUOROPHENOXY)PHENYL]METHANAMINE 95.00%
5MG
$ 499.36

Acrotein
4-(2-Fluorophenoxy)benzylamine 97%
5g
$ 742.50

Acrotein
4-(2-Fluorophenoxy)benzylamine 97%
1g
$ 247.50

Acrotein
4-(2-Fluorophenoxy)benzylamine 97%
0.5g
$ 165.00

Total 6 raw suppliers

Chemical Property of 1-[4-(2-Fluorophenoxy)phenyl]methanamine

Chemical Property:

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

1-[4-(2-FLUOROPHENOXY)PHENYL]METHANAMINE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

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

Technology Process of 1-[4-(2-Fluorophenoxy)phenyl]methanamine

There total 4 articles about 1-[4-(2-Fluorophenoxy)phenyl]methanamine 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%

: 864263-02-5
4-(2-fluorophenoxy)-benzylamine

Guidance literature:

Reference yield:

: 459-57-4
4-fluorobenzaldehyde

: 864263-02-5
4-(2-fluorophenoxy)-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

Reference yield:

: 367-12-4
2-fluorophenol

: 864263-02-5
4-(2-fluorophenoxy)-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