Basic information Safety Supplier Related

2,4,6-TRIS(4-BROMOPHENYL)-1,3,5-TRIAZINE

Basic information Safety Supplier Related

2,4,6-TRIS(4-BROMOPHENYL)-1,3,5-TRIAZINE Basic information

Product Name:
2,4,6-TRIS(4-BROMOPHENYL)-1,3,5-TRIAZINE
Synonyms:
  • 1,3,5-Triazine, 2,4,6-tris(4-bromophenyl)-
  • 2,4,6-TRIS(4-BROMOPHENYL)-1,3,5-TRIAZINE
  • 2,4,6-TRI-(4''-BROMOPHENYL)-1,3,5-TRIAZINE
  • 2,4,6-Tris(p-bromophenyl)triazine
  • 4,6-tris(4-bromophenyl)-1,3,5-Triazine
  • 2,4,6-Tris(4-Bromophenyl)-1,3,5-Triazine,>97%
  • 6-TRIS(4-BROMOPHENYL)-1
  • 2,4,6-TRIS(P-BROMOPHENYL)-S-TRIAZINE
CAS:
30363-03-2
MF:
C21H12Br3N3
MW:
546.05
Product Categories:
  • 1,3,5-triazine
Mol File:
30363-03-2.mol
More
Less

2,4,6-TRIS(4-BROMOPHENYL)-1,3,5-TRIAZINE Chemical Properties

Melting point:
>300 °C(Solv: chloroform (67-66-3))
Boiling point:
633.4±65.0 °C(Predicted)
Density 
1.741±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
Chloroform (Very Slightly, Heated)
form 
Solid
pka
-0.01±0.10(Predicted)
color 
White to Off-White
InChI
InChI=1S/C21H12Br3N3/c22-16-7-1-13(2-8-16)19-25-20(14-3-9-17(23)10-4-14)27-21(26-19)15-5-11-18(24)12-6-15/h1-12H
InChIKey
WZYVDGDZBNQVCF-UHFFFAOYSA-N
SMILES
N1=C(C2=CC=C(Br)C=C2)N=C(C2=CC=C(Br)C=C2)N=C1C1=CC=C(Br)C=C1
More
Less

Safety Information

HS Code 
2933.69.6050
More
Less

2,4,6-TRIS(4-BROMOPHENYL)-1,3,5-TRIAZINE Usage And Synthesis

Uses

2,?4,?6-?Tris-?(4-?bromophenyl)?[1,?3,?5]?triazine is a reagent used in the preparation of donor-acceptor dyads for enhancing the ability of charge carriers. Also a component in the discovery of dye-sensitized solar cells.

Synthesis

623-00-7

30363-03-2

(1) Synthesis of 2,4,6-tris(4-bromophenyl)-1,3,5-triazine: Trifluoromethanesulfonic acid (66.6 mmol, 9.99 g) was added to a dry two-necked flask under the protection of nitrogen and the flask was cooled down to 0 to 5°C in an ice bath. Subsequently, 4-bromobenzonitrile (19.6 mmol, 3.57 g) was slowly added and stirred continuously for 30 minutes at this temperature. After that, the reaction mixture was transferred to room temperature condition and continued stirring for 12 hours. After completion of the reaction, an appropriate amount of water was added to the mixture and neutralized with sodium hydroxide solution to neutral. Next, the organic layer was separated by extraction with a solvent mixture of chloroform and acetone (1:1, v/v). The organic layer was dried over anhydrous magnesium sulfate and the solvent was removed by distillation under reduced pressure to give the white solid product 2,4,6-tris(4-bromophenyl)-1,3,5-triazine (yield: 3.34 g, yield: 93.6%).

References

[1] Dalton Transactions, 2015, vol. 44, # 8, p. 3720 - 3723
[2] Chemistry of Materials, 2013, vol. 25, # 18, p. 3766 - 3771
[3] Patent: EP2808323, 2014, A1. Location in patent: Paragraph 0096-0097
[4] Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2009, vol. 48, # 12, p. 1766 - 1770
[5] Chemistry - A European Journal, 2018,

2,4,6-TRIS(4-BROMOPHENYL)-1,3,5-TRIAZINESupplier

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Email
market03@meryer.com
BeiJing Hwrk Chemicals Limted
Tel
0757-86329057 18934348241
Email
sales4.gd@hwrkchemical.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com
Wuhan Chemwish Technology Co., Ltd
Tel
86-027-67849912
Email
sales@chemwish.com
More
Less

2,4,6-TRIS(4-BROMOPHENYL)-1,3,5-TRIAZINE(30363-03-2)Related Product Information