4-(4-Fluorophenoxy)butan-1-amine

Base Information

Chemical Name:4-(4-Fluorophenoxy)butan-1-amine
CAS No.:873790-24-0
Molecular Formula:C₁₀H₁₄FNO
Molecular Weight:183.226
Hs Code.:
European Community (EC) Number:890-737-1

Synonyms:1-(4-aminobutoxy)-4-fluorobenzene;4-(4-fluorophenoxy)butan-1-amine;873790-24-0;HMS1745J22;AKOS000200976;EN300-31778

Suppliers and Price of 4-(4-Fluorophenoxy)butan-1-amine

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
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price

Total 1 raw suppliers

Chemical Property of 4-(4-Fluorophenoxy)butan-1-amine

Chemical Property:

XLogP3:1.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:183.105942232
Heavy Atom Count:13
Complexity:124

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC(=CC=C1OCCCCN)F

Technology Process of 4-(4-Fluorophenoxy)butan-1-amine

There total 2 articles about 4-(4-Fluorophenoxy)butan-1-amine 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:

: 948304-44-7
2-[4-(4-fluorophenoxy)butyl]isoindole-1,3-dione

: 873790-24-0
C₁₀H₁₄FNO

Guidance literature:: With hydrazine hydrate; In methanol; dichloromethane; at 20 ℃; for 24h;
DOI:10.1021/jm070270t

Reference yield:

: 371-41-5
4-Fluorophenol

: 873790-24-0
C₁₀H₁₄FNO

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / triphenylphosphine; diisopropyl azodicarboxylate / tetrahydrofuran / 20 °C

2: hydrazine hydrate / CH₂Cl₂; methanol / 24 h / 20 °C

With di-isopropyl azodicarboxylate; hydrazine hydrate; triphenylphosphine; In tetrahydrofuran; methanol; dichloromethane; 1: Mitsunobu coupling;
DOI:10.1021/jm070270t