Phenol, 2-mercapto-4-(phenylmethoxy)-

Base Information

Chemical Name:Phenol, 2-mercapto-4-(phenylmethoxy)-
CAS No.:110645-14-2
Molecular Formula:C13H12O2S
Molecular Weight:232.303
Hs Code.:
DSSTox Substance ID:DTXSID70475302
Wikidata:Q82305674
Mol file:110645-14-2.mol

Synonyms:Phenol, 2-mercapto-4-(phenylmethoxy)-;110645-14-2;SCHEMBL2128691;DTXSID70475302;AKOS034007835;Z2049917267

Suppliers and Price of Phenol, 2-mercapto-4-(phenylmethoxy)-

Supply Marketing:

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

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Chemical Property of Phenol, 2-mercapto-4-(phenylmethoxy)-

Chemical Property:

XLogP3:3.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:232.05580079
Heavy Atom Count:16
Complexity:204

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)COC2=CC(=C(C=C2)O)S

Technology Process of Phenol, 2-mercapto-4-(phenylmethoxy)-

There total 4 articles about Phenol, 2-mercapto-4-(phenylmethoxy)- 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:

: 321974-15-6
5-benzyloxybenzo[d][1,3]oxathiol-2-one

: 110645-14-2
4-(benzyloxy)-2-mercaptophenol

Guidance literature:: 5-benzyloxybenzo[d][1,3]oxathiol-2-one; With sodium hydroxide; In tetrahydrofuran; ethanol; water; at 20 ℃; for 1.33333h;

With hydrogenchloride; In tetrahydrofuran; ethanol; water; at 0 ℃;

Reference yield:

: 7735-56-0
5-hydroxybenzo[d][1,3]oxathiol-2-one

: 110645-14-2
4-(benzyloxy)-2-mercaptophenol

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium iodide / acetone / 0.5 h / 0 °C

1.2: 36 h / 20 °C / Inert atmosphere

2.1: ethanol; potassium hydroxide / tetrahydrofuran / 6 h / Inert atmosphere

With ethanol; potassium iodide; potassium hydroxide; In tetrahydrofuran; acetone;
DOI:10.1016/j.ejmech.2014.04.081

Reference yield:

: 106-51-4
p-benzoquinone

: 110645-14-2
4-(benzyloxy)-2-mercaptophenol

Guidance literature:: Multi-step reaction with 3 steps

1.1: hydrogenchloride; acetic acid / 5 h / 20 °C / Reflux

2.1: potassium iodide / acetone / 0.5 h / 0 °C

2.2: 36 h / 20 °C / Inert atmosphere

3.1: ethanol; potassium hydroxide / tetrahydrofuran / 6 h / Inert atmosphere

With hydrogenchloride; ethanol; acetic acid; potassium iodide; potassium hydroxide; In tetrahydrofuran; acetone;
DOI:10.1016/j.ejmech.2014.04.081