2-[4-(3,4-Dichlorobenzyloxy)phenylethanol

Base Information

Chemical Name:2-[4-(3,4-Dichlorobenzyloxy)phenylethanol
CAS No.:188928-11-2
Molecular Formula:C15H14Cl2O2
Molecular Weight:297.181
Hs Code.:
DSSTox Substance ID:DTXSID70400659
Wikidata:Q82203667
Mol file:188928-11-2.mol

Synonyms:2-[4-(3,4-Dichlorobenzyloxy)phenylethanol;188928-11-2;2-[4-[(3,4-dichlorophenyl)methoxy]phenyl]ethanol;2-{4-[(3,4-Dichlorobenzyl)oxy]phenyl}ethanol;Benzeneethanol, 4-[(3,4-dichlorophenyl)methoxy]-;2-(4-((3,4-dichlorobenzyl)oxy)phenyl)ethanol;DTXSID70400659;AKOS030240448;FT-0666553

Suppliers and Price of 2-[4-(3,4-Dichlorobenzyloxy)phenylethanol

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

TRC
2-[4-(3,4-Dichlorobenzyloxy)phenylethanol
50mg
$ 105.00

Medical Isotopes, Inc.
2-[4-(3,4-Dichlorobenzyloxy)-phenylethanol
0.5 g
$ 1760.00

Biosynth Carbosynth
2-[4-(3,4-Dichlorobenzyloxy)phenylethanol
250 mg
$ 462.50

Biosynth Carbosynth
2-[4-(3,4-Dichlorobenzyloxy)phenylethanol
100 mg
$ 255.00

Biosynth Carbosynth
2-[4-(3,4-Dichlorobenzyloxy)phenylethanol
50 mg
$ 140.00

Biosynth Carbosynth
2-[4-(3,4-Dichlorobenzyloxy)phenylethanol
1 g
$ 1528.80

Biosynth Carbosynth
2-[4-(3,4-Dichlorobenzyloxy)phenylethanol
500 mg
$ 840.00

American Custom Chemicals Corporation
2-[4-(3,4-DICHLOROBENZYLOXY)-PHENYL]ETHANOL 95.00%
5MG
$ 500.36

Total 4 raw suppliers

Chemical Property of 2-[4-(3,4-Dichlorobenzyloxy)phenylethanol

Chemical Property:

PSA：29.46000
LogP:4.10720
Solubility.:Acetone, Chloroform, Dichloromethane, Ethyl Acetate, Methanol
XLogP3:4.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:296.0370851
Heavy Atom Count:19
Complexity:255

Purity/Quality:

97% ^*data from raw suppliers

2-[4-(3,4-Dichlorobenzyloxy)phenylethanol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1CCO)OCC2=CC(=C(C=C2)Cl)Cl
Uses 2-[4-(3,4-Dichlorobenzyloxy)phenylethanol can be used for preparation of S-[(benzyloxyphenyl)alkyl]isothiourea derivatives as inhibitors of Na+-Ca2+ exchanger.

Technology Process of 2-[4-(3,4-Dichlorobenzyloxy)phenylethanol

There total 1 articles about 2-[4-(3,4-Dichlorobenzyloxy)phenylethanol 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: 83.0%

: 501-94-0
p-hydroxyphenethyl alcohol

: 102-47-6
3,4-Dichlorophenylmethyl chloride

: 188928-11-2
2-(4-(3,4-dichlorobenzyloxy)phenyl)ethanol

Guidance literature:: With potassium carbonate; In acetone; for 24h; Reflux;
DOI:10.1016/j.ejmech.2011.05.018

Reference yield: 64.0%

: 188928-11-2
2-(4-(3,4-dichlorobenzyloxy)phenyl)ethanol

: 1334930-93-6
2-(4-(3,4-dichlorobenzyloxy)phenyl)acetaldehyde

Guidance literature:: With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; sodium bromite trihydrate; sodium hydrogencarbonate; In dichloromethane; water; at 0 - 20 ℃; for 0.5h; pH=8.6;
DOI:10.1016/j.ejmech.2011.05.018

Reference yield:

: 188928-11-2
2-(4-(3,4-dichlorobenzyloxy)phenyl)ethanol

: 1334931-22-4
ethyl 2-(4-chlorobenzamido)-5-(4-(3,4-dichlorobenzyloxy)phenyl)thiophene-3-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: sodium bromite trihydrate; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; sodium hydrogencarbonate / dichloromethane; water / 0.5 h / 0 - 20 °C / pH 8.6

2: sulfur; triethylamine / ethanol / 60 °C

3: triethylamine / dichloromethane / 20 °C

With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; sodium bromite trihydrate; sodium hydrogencarbonate; sulfur; triethylamine; In ethanol; dichloromethane; water;
DOI:10.1016/j.ejmech.2011.05.018