3-(Pentyloxy)phenol

Base Information

Chemical Name:3-(Pentyloxy)phenol
CAS No.:18979-73-2
Molecular Formula:C11H16 O2
Molecular Weight:180.247
Hs Code.:2909500000
DSSTox Substance ID:DTXSID00576952
Nikkaji Number:J945.230C
Wikidata:Q82466836
Mol file:18979-73-2.mol

Synonyms:3-(Pentyloxy)phenol;18979-73-2;3-n-pentoxyphenol;3-pentoxyphenol;M-PENTOXYPHENOL;3-pentyloxyphenol;3-(n-Pentoxy)phenol;SCHEMBL3636219;DTXSID00576952;IOOCVIRRKFNHEL-UHFFFAOYSA-N

Suppliers and Price of 3-(Pentyloxy)phenol

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

Total 3 raw suppliers

Chemical Property of 3-(Pentyloxy)phenol

Chemical Property:

Refractive Index:1.4930 (estimate)
Boiling Point:273.08°C (rough estimate)
PSA：29.46000
Density:1.0044 (rough estimate)
LogP:2.96120
Water Solubility.:383.9mg/L(30 oC)
XLogP3:3.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:180.115029749
Heavy Atom Count:13
Complexity:125

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCCOC1=CC=CC(=C1)O

Technology Process of 3-(Pentyloxy)phenol

There total 7 articles about 3-(Pentyloxy)phenol 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: 92.0%

: 110-53-2
1-Bromopentane

: 108-46-3
recorcinol

: 18979-73-2
3-(n-pentoxy)phenol

Guidance literature:

Reference yield:

: 108-46-3
recorcinol

: 18979-73-2
3-(n-pentoxy)phenol

Guidance literature:: DOI:10.1021/ja01360a025

Reference yield:

: 161006-18-4
3-((tert-butyldimethylsilyl)oxy)phenol

: 18979-73-2
3-(n-pentoxy)phenol

Guidance literature:: Multi-step reaction with 2 steps

1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 12 h / 0 °C / Inert atmosphere

2: tetrabutyl ammonium fluoride / tetrahydrofuran / 20 °C / Inert atmosphere

With di-isopropyl azodicarboxylate; tetrabutyl ammonium fluoride; triphenylphosphine; In tetrahydrofuran; 1: |Mitsunobu Displacement;
DOI:10.1021/acs.jmedchem.1c01078