4-(2-Methoxyphenyl)butan-1-OL

Base Information

Chemical Name:4-(2-Methoxyphenyl)butan-1-OL
CAS No.:10493-38-6
Molecular Formula:C11H16O2
Molecular Weight:180.247
Hs Code.:
DSSTox Substance ID:DTXSID00600044
Wikidata:Q82496005
Mol file:10493-38-6.mol

Synonyms:10493-38-6;4-(2-METHOXYPHENYL)BUTAN-1-OL;Benzenebutanol, 2-methoxy-;2-methoxybenzenebutanol;2-Methoxy-benzenebutanol;hydroxybutylanisol;2-methoxybenzenbutanol;SCHEMBL7650103;DTXSID00600044;LICCCCCCEBHYTF-UHFFFAOYSA-N;AKOS006317686;CS-0440291;F80290

Suppliers and Price of 4-(2-Methoxyphenyl)butan-1-OL

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

Labseeker
BENZENEBUTANOL,2-METHOXY- 95
10g
$ 3208.00

American Custom Chemicals Corporation
2-METHOXY-BENZENEBUTANOL 95.00%
5MG
$ 497.62

Acrotein
2-Methoxy-benzenebutanol 97%
0.5g
$ 330.00

Acrotein
2-Methoxy-benzenebutanol 97%
0.25g
$ 220.00

Total 2 raw suppliers

Chemical Property of 4-(2-Methoxyphenyl)butan-1-OL

Chemical Property:

PSA：29.46000
LogP:2.01020
XLogP3:2.7
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

BENZENEBUTANOL,2-METHOXY- 95 ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC=CC=C1CCCCO

Technology Process of 4-(2-Methoxyphenyl)butan-1-OL

There total 7 articles about 4-(2-Methoxyphenyl)butan-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%

: 92587-67-2
4-(2-methoxyphenyl)but-3-yn-1-ol

: 10493-38-6
4-(2-methoxyphenyl)-1-butanol

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In methanol; at 20 ℃; for 16h; Inert atmosphere;
DOI:10.1016/j.bmcl.2011.08.029

Reference yield:

: 33209-76-6
Ethyl 4-(2-Methoxyphenyl)-butanoate

: 10493-38-6
4-(2-methoxyphenyl)-1-butanol

Guidance literature:: With lithium aluminium tetrahydride;

Reference yield:

: 529-28-2
4-iodoanisol

: 10493-38-6
4-(2-methoxyphenyl)-1-butanol

Guidance literature:: Multi-step reaction with 2 steps

1: copper(l) iodide; trans-bis(triphenylphosphine)palladium dichloride; triethylamine / 24 h / 0 °C / Inert atmosphere; Reflux

2: palladium 10% on activated carbon; hydrogen / methanol / 16 h / 20 °C / Inert atmosphere

With copper(l) iodide; trans-bis(triphenylphosphine)palladium dichloride; palladium 10% on activated carbon; hydrogen; triethylamine; In methanol; 1: Sonogashira coupling;
DOI:10.1016/j.bmcl.2011.08.029