1,3-Bis(4-phenoxyphenoxy)benzene

Base Information

Chemical Name:1,3-Bis(4-phenoxyphenoxy)benzene
CAS No.:1638-12-6
Molecular Formula:C30H22 O4
Molecular Weight:446.502
Hs Code.:
European Community (EC) Number:216-669-9
DSSTox Substance ID:DTXSID4061838
Nikkaji Number:J195.270F
Wikidata:Q81989699
Mol file:1638-12-6.mol

Synonyms:1,3-Bis(4-phenoxyphenoxy)benzene;1638-12-6;Benzene, 1,3-bis(4-phenoxyphenoxy)-;EINECS 216-669-9;SCHEMBL3888963;DTXSID4061838

Suppliers and Price of 1,3-Bis(4-phenoxyphenoxy)benzene

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 7 raw suppliers

Chemical Property of 1,3-Bis(4-phenoxyphenoxy)benzene

Chemical Property:

Vapor Pressure:5.74E-12mmHg at 25°C
Melting Point:88-89 °C
Boiling Point:559.3°Cat760mmHg
Flash Point:129.7°C
Density:1.2g/cm³
XLogP3:8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:8
Exact Mass:446.15180918
Heavy Atom Count:34
Complexity:506

Purity/Quality:: 99% ^*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=C(C=C2)OC3=CC(=CC=C3)OC4=CC=C(C=C4)OC5=CC=CC=C5

Technology Process of 1,3-Bis(4-phenoxyphenoxy)benzene

There total 5 articles about 1,3-Bis(4-phenoxyphenoxy)benzene 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:

: 150-19-6
O-methylresorcine

: 1638-12-6
1,3-bis(4-phenoxyphenoxy)benzene

Guidance literature:: Multi-step reaction with 3 steps

1: (i) aq. KOH, (ii) /BRN= 1308972/, Cu, (heating)

2: aq. HBr, AcOH

3: (i) aq. KOH, (ii) /BRN= 1308972/, Cu, (heating)

With hydrogen bromide; acetic acid;
DOI:10.1021/jo01079a029

Reference yield:

: 101-55-3
4-Bromodiphenyl ether

: 1638-12-6
1,3-bis(4-phenoxyphenoxy)benzene

Guidance literature:: Multi-step reaction with 3 steps

1: (i) aq. KOH, (ii) /BRN= 1308972/, Cu, (heating)

2: aq. HBr, AcOH

3: (i) aq. KOH, (ii) /BRN= 1308972/, Cu, (heating)

With hydrogen bromide; acetic acid;
DOI:10.1021/jo01079a029

Reference yield:

: 108368-36-1
1-(m-Methoxy-phenoxy)-4-phenoxy-benzol

: 1638-12-6
1,3-bis(4-phenoxyphenoxy)benzene

Guidance literature:: Multi-step reaction with 2 steps

1: aq. HBr, AcOH

2: (i) aq. KOH, (ii) /BRN= 1308972/, Cu, (heating)

With hydrogen bromide; acetic acid;
DOI:10.1021/jo01079a029