Benzene, 1,2,3-tribromo-4-(2,3,4-tribromophenoxy)-

Base Information

Chemical Name:Benzene, 1,2,3-tribromo-4-(2,3,4-tribromophenoxy)-
CAS No.:182677-28-7
Molecular Formula:C₁₂H₄Br₆O
Molecular Weight:643.587
Hs Code.:
UNII:EW9QWZ8VGN
DSSTox Substance ID:DTXSID60550652
Nikkaji Number:J201.375D
Wikidata:Q27277393
Mol file:182677-28-7.mol

Synonyms:182677-28-7;2,2',3,3',4,4'-Hexabromodiphenyl ether;PBDE 128;Benzene, 1,2,3-tribromo-4-(2,3,4-tribromophenoxy)-;EW9QWZ8VGN;UNII-EW9QWZ8VGN;1,1'-Oxybis[2,3,4-tribromo-benzene];1,2,3-tribromo-4-(2,3,4-tribromophenoxy)benzene;SCHEMBL4190024;DTXSID60550652;WFLVELCLEGVBIH-UHFFFAOYSA-N;1,1'-Oxybis(2,3,4-tribromobenzene);NS00074005;Q27277393

Suppliers and Price of Benzene, 1,2,3-tribromo-4-(2,3,4-tribromophenoxy)-

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
1,1''-Oxybis[2,3,4-tribromo-benzene]
100mg
$ 1760.00

Medical Isotopes, Inc.
1,1??-Oxybis[2,3,4-tribromo-benzene]
10 mg
$ 700.00

Total 4 raw suppliers

Chemical Property of Benzene, 1,2,3-tribromo-4-(2,3,4-tribromophenoxy)-

Chemical Property:

Boiling Point:481.1±45.0 °C(Predicted)
PSA：9.23000
Density:2.502±0.06 g/cm3(Predicted)
LogP:8.05390
XLogP3:7.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:643.53009
Heavy Atom Count:19
Complexity:276

Purity/Quality:

99% ^*data from raw suppliers

1,1''-Oxybis[2,3,4-tribromo-benzene] ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=C(C(=C1OC2=C(C(=C(C=C2)Br)Br)Br)Br)Br)Br
Uses 1,1''-Oxybis[2,3,4-tribromo-benzene] is a polybrominated diphenyl ether (PBDE) used as a flame retardant.

Technology Process of Benzene, 1,2,3-tribromo-4-(2,3,4-tribromophenoxy)-

There total 3 articles about Benzene, 1,2,3-tribromo-4-(2,3,4-tribromophenoxy)- 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: 12.0%

: 6903-63-5
1-bromo-3-(3-bromophenoxy)benzene

: 182677-30-1
2,2',3,4,4'5'-hexabromodiphenyl ether

: 182677-28-7
2,2',3,3',4,4'-hexabromodiphenyl ether

: 68631-49-2
2,2',4,4',5,5'-hexabromobiphenyl ether

Guidance literature:: With bromine; iron; In tetrachloromethane; Heating;

Reference yield:

: 591-20-8
3-Bromophenol

: 182677-28-7
2,2',3,3',4,4'-hexabromodiphenyl ether

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) potassium hydroxide, 2.) copper bronze / 1.) 10 min, 2.) 170 deg C, 2 h

2: 12 percent / bromine, iron / CCl₄ / Heating

With potassium hydroxide; bromine; iron; copper; In tetrachloromethane;

Reference yield:

: 108-36-1
1,3-dibromobenzene

: 182677-28-7
2,2',3,3',4,4'-hexabromodiphenyl ether

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) potassium hydroxide, 2.) copper bronze / 1.) 10 min, 2.) 170 deg C, 2 h

2: 12 percent / bromine, iron / CCl₄ / Heating

With potassium hydroxide; bromine; iron; copper; In tetrachloromethane;