CAS 4316-58-9

Tris(4-bromophenyl)amine

Description:

Tris(4-bromophenyl)amine, with the CAS number 4316-58-9, is an organic compound characterized by its structure, which consists of a central nitrogen atom bonded to three 4-bromophenyl groups. This compound is typically a solid at room temperature and exhibits a crystalline form. It is known for its stability and can be used in various applications, including as a building block in organic synthesis and in the development of organic electronic materials. The presence of bromine atoms enhances its electronic properties, making it useful in the field of materials science, particularly in the design of semiconductors and light-emitting devices. Additionally, Tris(4-bromophenyl)amine may exhibit interesting photophysical properties, which can be leveraged in optoelectronic applications. Its solubility is generally moderate in organic solvents, and it may show varying degrees of reactivity depending on the conditions. Safety precautions should be taken when handling this compound, as with many brominated organic substances, due to potential toxicity and environmental concerns.

Formula: C₁₈H₁₂Br₃N

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

InChI key: InChIKey=ZRXVCYGHAUGABY-UHFFFAOYSA-N

SMILES: N(C1=CC=C(Br)C=C1)(C2=CC=C(Br)C=C2)C3=CC=C(Br)C=C3

Synonyms:

• 4,4',4"-Tribromotriphenylamine
• 4,4′,4′′-Tribromotriphenylamine
• 4-Bromo-N,N-bis(4-bromophenyl)benzenamine
• 4-bromo-N,N-bis(4-bromophenyl)aniline
• Benzenamine, 4-bromo-N,N-bis(4-bromophenyl)-
• N,N-Bis(4-bromophenyl)-4-bromoaniline
• N,N-Diphenyl-4,4′,4′′-tribromoaniline
• NSC 86666
• Tri(4-bromophenyl) amine
• Tri(p-bromophenyl)amine
• Triphenylamine, 4,4′,4′′-tribromo-
• Tris(p-bromophenyl)amine

Tris(4-bromophenyl)amine

CAS: 4316-58-9

Formula: C₁₈H₁₂Br₃N

Purity: >98.0%(GC)

Color and Shape: White to Almost white powder to crystal

Molecular weight: 482.01

Ref: 3B-T1361

Tris(4-bromophenyl)amine, 98%

CAS: 4316-58-9

Tris(4-bromophenyl)amine was used in the synthesis of porous luminescent covalent--organic polymers (COPs) This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa

Formula: C₁₈H₁₂Br₃N

Purity: 98%

Color and Shape: White to pale green, Powder

Molecular weight: 482.01

Ref: 02-H60860

Tris(4-bromophenyl)amine

CAS: 4316-58-9

Formula: C₁₈H₁₂Br₃N

Purity: 97%

Color and Shape: Solid

Molecular weight: 482.0066

Ref: IN-DA003V7I

Tris(4-bromophenyl)amine

CAS: 4316-58-9

Tris(4-bromophenyl)amine

Formula: C₁₈H₁₂Br₃N

Purity: 98%

Color and Shape: off-white solid

Molecular weight: 482.00658g/mol

Ref: 54-OR70090

Tris(4-bromophenyl)amine (purified by sublimation)

CAS: 4316-58-9

Formula: C₁₈H₁₂Br₃N

Purity: >99.0%(GC)

Color and Shape: White to Almost white powder to crystal

Molecular weight: 482.01

Ref: 3B-T3777

Tris(4-bromophenyl)amine

CAS: 4316-58-9

Purity: 97%

Color and Shape: Solid

Molecular weight: 482.01300048828125

Ref: 10-F790979

Tris(4-bromophenyl)amine

CAS: 4316-58-9

Tris(4-bromophenyl)amine is a chemical compound that is used as an intermediate in the synthesis of other compounds. It has been studied for its electrochemical properties, which include its stability and ability to react with ethyl diazoacetate. The reaction mechanism of tris(4-bromophenyl)amine has been studied using electrochemical techniques, including kinetic and spectroscopic studies. Tris(4-bromophenyl)amine reacts with acid to produce nitrite ions and bromine water, which can then react with ethyl diazoacetate to produce aryl diazonium salts such as 3-nitrophenol. This process can be repeated multiple times to form aryl diazonium salts such as 6-nitrophenol or 5-nitrophenol. The electron reduction potential of tris(4-bromophenyl)amine is low enough that it can be easily oxid

Formula: C₁₈H₁₂Br₃N

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 482.01 g/mol

Ref: 3D-FT62286