(3-Aminophenyl)(4-fluorophenyl)methanone

Base Information

Chemical Name:(3-Aminophenyl)(4-fluorophenyl)methanone
CAS No.:62261-29-4
Molecular Formula:C13H10FNO
Molecular Weight:215.227
Hs Code.:
DSSTox Substance ID:DTXSID10442437
Wikidata:Q82259710

Synonyms:62261-29-4;(3-aminophenyl)(4-fluorophenyl)methanone;Methanone, (3-aminophenyl)(4-fluorophenyl)-;SBB046043;SCHEMBL10455398;DTXSID10442437;YELJAOYXDLKMGA-UHFFFAOYSA-N;3-[(4-Fluorophenyl)carbonyl]aniline;STK695719;AKOS000275275;CCG-324118;NCGC00332102-01;AB01325964-02

Suppliers and Price of (3-Aminophenyl)(4-fluorophenyl)methanone

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of (3-Aminophenyl)(4-fluorophenyl)methanone

Chemical Property:

PSA：43.09000
LogP:3.22010
XLogP3:2.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:215.074642105
Heavy Atom Count:16
Complexity:248

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC(=C1)N)C(=O)C2=CC=C(C=C2)F

Technology Process of (3-Aminophenyl)(4-fluorophenyl)methanone

There total 5 articles about (3-Aminophenyl)(4-fluorophenyl)methanone 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: 96.0%

: 16574-53-1
(4-fluorophenyl)(3-nitrophenyl)methanone

: 62261-29-4
(3-aminophenyl)(4-fluorophenyl)methanone

Guidance literature:: With iron; ammonium chloride; In Isopropyl acetate; at 80 ℃; for 3h;

Reference yield: 70.0%

: 3-aminophenyl zinc iodide

: 403-43-0
4-fluorobenzoyl chloride

: 62261-29-4
(3-aminophenyl)(4-fluorophenyl)methanone

Guidance literature:: With copper(l) iodide; lithium chloride; In tetrahydrofuran; at 0 ℃; for 3h; Inert atmosphere;
DOI:10.1016/j.tetlet.2015.01.053

Reference yield:

: 462-06-6
fluorobenzene

: 62261-29-4
(3-aminophenyl)(4-fluorophenyl)methanone

Guidance literature:: Multi-step reaction with 2 steps

1: AlCl₃ / 1,2-dichloro-ethane / 4 h / Ambient temperature

2: Fe, glacial AcOH / 80 °C

With aluminium trichloride; iron; acetic acid; In 1,2-dichloro-ethane;
DOI:10.1021/jo970571i