3-(2-Aminophenoxy)propan-1-ol

Base Information

Chemical Name:3-(2-Aminophenoxy)propan-1-ol
CAS No.:920268-18-4
Molecular Formula:C9H13NO2
Molecular Weight:167.208
Hs Code.:
DSSTox Substance ID:DTXSID60607372
Wikidata:Q82506378

Synonyms:3-(2-aminophenoxy)propan-1-ol;920268-18-4;SCHEMBL13884056;DTXSID60607372;EN300-1295026

Suppliers and Price of 3-(2-Aminophenoxy)propan-1-ol

Supply Marketing:

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

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Chemical Property of 3-(2-Aminophenoxy)propan-1-ol

Chemical Property:

XLogP3:0.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:167.094628657
Heavy Atom Count:12
Complexity:119

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C(=C1)N)OCCCO

Technology Process of 3-(2-Aminophenoxy)propan-1-ol

There total 2 articles about 3-(2-Aminophenoxy)propan-1-ol 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%

: 38340-87-3
3-(2-nitrophenoxy)propan-1-ol

: 920268-18-4
3-(2-aminophenoxy)propan-1-ol

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethanol; ethyl acetate; at 20 ℃; for 48h; under 760 Torr;
DOI:10.1021/ja065264l

Reference yield:

: 1493-27-2,127723-77-7
ortho-nitrofluorobenzene

: 920268-18-4
3-(2-aminophenoxy)propan-1-ol

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydride / tetrahydrofuran

2: 10% Pd/C; hydrogen / ethanol

With 10% Pd/C; hydrogen; sodium hydride; In tetrahydrofuran; ethanol;
DOI:10.1016/j.bmcl.2012.09.035