| Identification | More | [Name]
Tris(4-bromophenyl)amine | [CAS]
4316-58-9 | [Synonyms]
TRIS(4-BROMOPHENYL)AMINE
TRIS(4-BROMOPHENYL)AMIN
4,4',4"-Tribromotriphenylamine
TRI(4-BROMOPHENYL)AMINE
4,4',4''-Nitrilotris(1-bromobenzene)
N,N-Bis(4-bromophenyl)-4-bromoaniline | [EINECS(EC#)]
628-703-3 | [Molecular Formula]
C18H12Br3N | [MDL Number]
MFCD00009665 | [Molecular Weight]
482.01 | [MOL File]
4316-58-9.mol |
| Chemical Properties | Back Directory | [Appearance]
pale green powder | [Melting point ]
141-143 °C (lit.) | [Boiling point ]
514.9±45.0 °C(Predicted) | [density ]
1.790±0.06 g/cm3(Predicted) | [Fp ]
100°C | [storage temp. ]
Refrigerator | [solubility ]
Soluble in toluene. | [form ]
powder to crystal | [pka]
-4.91±0.50(Predicted) | [color ]
White to Almost white | [Stability:]
Stable. Incompatible with strong oxidizing agents. | [InChI]
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 | [InChIKey]
ZRXVCYGHAUGABY-UHFFFAOYSA-N | [SMILES]
C1(N(C2=CC=C(Br)C=C2)C2=CC=C(Br)C=C2)=CC=C(Br)C=C1 | [CAS DataBase Reference]
4316-58-9(CAS DataBase Reference) |
| Safety Data | Back Directory | [Symbol(GHS) ]
GHS07 | [Signal word ]
Warning | [Hazard statements ]
H315-H319-H335 | [Precautionary statements ]
P261-P264-P271-P280-P302+P352-P305+P351+P338 | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S37/39:Wear suitable gloves and eye/face protection . | [WGK Germany ]
3
| [HS Code ]
29214990 | [Storage Class]
11 - Combustible Solids | [Hazard Classifications]
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 |
| Hazard Information | Back Directory | [Chemical Properties]
pale green powder | [Uses]
Tris(4-bromophenyl)amine was used in the synthesis of porous luminescent covalent--organic polymers (COPs) | [Application]
Tri(4-bromophenyl)amine is a key raw material for the synthesis of a novel three-branched triphenylamine organoboron complex (TPAB). TPAB can be successfully synthesized through Suzuki coupling, condensation, and coordination reactions with 4-aminophenylboronic acid pinacol ester, 4-diethylaminosalicylaldehyde, and boron trifluoride etherate. |
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