1-Phenoxy-3-phenylmercaptobenzene

Base Information

Chemical Name:1-Phenoxy-3-phenylmercaptobenzene
CAS No.:7372-99-8
Molecular Formula:C18H14OS
Molecular Weight:278.3682
Hs Code.:
DSSTox Substance ID:DTXSID3064647
Nikkaji Number:J1.583.046H
Wikidata:Q81991735

Synonyms:Phenyl m-(phenylthio)phenyl ether;1-Phenoxy-3-phenylmercaptobenzene;7372-99-8;Benzene, 1-phenoxy-3-(phenylthio)-;C18H14OS;DTXSID3064647;SCHEMBL16890630;1-Phenoxy-3-(phenylthio)benzene;C18-H14-O-S

Suppliers and Price of 1-Phenoxy-3-phenylmercaptobenzene

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 1 raw suppliers

Chemical Property of 1-Phenoxy-3-phenylmercaptobenzene

Chemical Property:

Vapor Pressure:8.18E-07mmHg at 25°C
Boiling Point:418.1°Cat760mmHg
Flash Point:206.6°C
Density:1.2g/cm³
XLogP3:5.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:278.07653624
Heavy Atom Count:20
Complexity:269

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)OC2=CC(=CC=C2)SC3=CC=CC=C3

Technology Process of 1-Phenoxy-3-phenylmercaptobenzene

There total 3 articles about 1-Phenoxy-3-phenylmercaptobenzene 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:

: 6876-00-2
3-bromodiphenyl ether

: 108-98-5
thiophenol

: 7372-99-8
(3-phenoxyphenyl)(phenyl)sulfane

Guidance literature:: With copper(l) iodide; potassium carbonate; In 1-methyl-pyrrolidin-2-one; at 170 ℃; for 6h; Inert atmosphere;

Reference yield:

: 1073-06-9
3-fluorobromobenzene

: 7372-99-8
(3-phenoxyphenyl)(phenyl)sulfane

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / 1-methyl-pyrrolidin-2-one / 12 h / 200 °C / Inert atmosphere

2: copper(l) iodide; potassium carbonate / 1-methyl-pyrrolidin-2-one / 6 h / 170 °C / Inert atmosphere

With copper(l) iodide; potassium carbonate; In 1-methyl-pyrrolidin-2-one;

Reference yield:

: 108-95-2,27073-41-2
phenol

: 7372-99-8
(3-phenoxyphenyl)(phenyl)sulfane

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / 1-methyl-pyrrolidin-2-one / 12 h / 200 °C / Inert atmosphere

2: copper(l) iodide; potassium carbonate / 1-methyl-pyrrolidin-2-one / 6 h / 170 °C / Inert atmosphere

With copper(l) iodide; potassium carbonate; In 1-methyl-pyrrolidin-2-one;