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230219

Sigma-Aldrich

Tris(4-bromophenyl)amine

98%

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About This Item

Linear Formula:
(BrC6H4)3N
CAS Number:
4316-58-9
Molecular Weight:
482.01
MDL number:
MFCD00009665
UNSPSC Code:
12352100
PubChem Substance ID:
24853785
NACRES:
NA.22

Assay

98%

mp

141-143 °C (lit.)

SMILES string

Brc1ccc(cc1)N(c2ccc(Br)cc2)c3ccc(Br)cc3

InChI

1S/C18H12Br3N/c19-13-1-7-16(8-2-13)22(17-9-3-14(20)4-10-17)18-11-5-15(21)6-12-18/h1-12H

InChI key

ZRXVCYGHAUGABY-UHFFFAOYSA-N

Application

Tris(4-bromophenyl)amine was used in the synthesis of porous luminescent covalent--organic polymers (COPs).

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

230219-50G:
230219-BULK:
230219-10G:
230219-VAR:

Certificates of Analysis (COA)

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Zhonghua Xiang et al.
Macromolecular rapid communications, 33(14), 1184-1190 (2012-04-18)
Three porous luminescent covalent--organic polymers (COPs) have been synthesized through self-polycondensation of the monomers of tris(4-bromophenyl)amine, 1,3,5-tris(4-bromophenyl)benzene, and 2,4,6-tris-(4-bromo-phenyl)-[1,3,5]triazine by using Ni-catalyzed Yamamoto reaction. All the COP materials possess not only high Brunauer-Emmett-Teller (BET) specific surface area of about 2000
S A Ponomarenko et al.
Faraday discussions, 174, 313-339 (2014-10-04)
This contribution describes recent progress in the design, synthesis and properties of solution-processible star-shaped oligomers and their application in organic photovoltaics. Even though alternative chemistry has been used to design such oligomers, the most successful approach is based on a

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