beta-Amino-4-(pentyloxy)benzeneethanol

Base Information

Chemical Name:beta-Amino-4-(pentyloxy)benzeneethanol
CAS No.:157142-49-9
Molecular Formula:C₁₃H₂₁NO₂
Molecular Weight:223.315
Hs Code.:
DSSTox Substance ID:DTXSID801295141

Synonyms:DTXSID801295141;AKOS005638893;157142-49-9;2-amino-2-[4-(pentyloxy)phenyl]-1-ethanol

Suppliers and Price of beta-Amino-4-(pentyloxy)benzeneethanol

Supply Marketing:

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

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Chemical Property of beta-Amino-4-(pentyloxy)benzeneethanol

Chemical Property:

XLogP3:1.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:7
Exact Mass:223.157228913
Heavy Atom Count:16
Complexity:167

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCCOC1=CC=C(C=C1)C(CO)N

Technology Process of beta-Amino-4-(pentyloxy)benzeneethanol

There total 3 articles about beta-Amino-4-(pentyloxy)benzeneethanol 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: 75.0%

: 1359764-19-4
C₁₅H₂₁NO₄

: 157142-49-9
2-amino-2-(4-(pentyloxy)phenyl)ethanol

Guidance literature:: C₁₅H₂₁NO₄; With sodium tetrahydroborate; iodine; In tetrahydrofuran; Reflux;

With sodium hydroxide; at 100 ℃;
DOI:10.1021/jf204778v

Reference yield:

: 2050-04-6
(pentyloxy)benzene

: 157142-49-9
2-amino-2-(4-(pentyloxy)phenyl)ethanol

Guidance literature:: Multi-step reaction with 3 steps

1.1: aluminum (III) chloride / dichloromethane / 20 °C / Inert atmosphere

1.2: 5 - 20 °C / Inert atmosphere

2.1: hydroxylamine hydrochloride / ethanol / Reflux

3.1: sodium tetrahydroborate; iodine / tetrahydrofuran / Reflux

3.2: 100 °C

With aluminum (III) chloride; sodium tetrahydroborate; hydroxylamine hydrochloride; iodine; In tetrahydrofuran; ethanol; dichloromethane; 1.1: Friedel Crafts acylation / 1.2: Friedel Crafts acylation;
DOI:10.1021/jf204778v

Reference yield:

: 1256482-10-6
ethyl 2-oxo-2-(4-(pentyloxy)phenyl)acetate

: 157142-49-9
2-amino-2-(4-(pentyloxy)phenyl)ethanol

Guidance literature:: Multi-step reaction with 2 steps

1.1: hydroxylamine hydrochloride / ethanol / Reflux

2.1: sodium tetrahydroborate; iodine / tetrahydrofuran / Reflux

2.2: 100 °C

With sodium tetrahydroborate; hydroxylamine hydrochloride; iodine; In tetrahydrofuran; ethanol;
DOI:10.1021/jf204778v