ChemicalBook--->CAS DataBase List--->58047-42-0

58047-42-0

58047-42-0 Structure

58047-42-0 Structure
IdentificationBack Directory
[Name]

4-Bromo-4',4''-dimethyltriphenylamine
[CAS]

58047-42-0
[Synonyms]

BDMTPA
4-broMo -4',4''- twoMe
4-Bromo-N,N-di-p-tolylaniline
Di-p-tolyl-p-bromophenylamine
4-Bromo-N,N-dip-tolylbenzenamine
(4-Bromo-phenyl)-di-p-tolyl-amine
4-Bromo-N,N-dip-tolylbenzenamine ,97%
4-BROMO-4'',4''-DIMETHYLTRIPHENYLAMINE
4-broMo -4',4''- twoMethyl threeaniline
4-Bromo-4',4''-dimethyltriphenylamine >
4-Bromo-N,N-bis(4-methylphenyl)benzenamine
Benzenamine,4-bromo-N,N-bis(4-methylphenyl)-
4-BROMO-4'',4''-DIMETHYLTRIPHENYLAMINE,95.0+%(GC)
N-(4-bromophenyl)-4-methyl-N-(4-methylphenyl)aniline
[Molecular Formula]

C20H18BrN
[MDL Number]

MFCD03093258
[MOL File]

58047-42-0.mol
[Molecular Weight]

352.27
Chemical PropertiesBack Directory
[Melting point ]

102 °C
[Boiling point ]

459.9±45.0 °C(Predicted)
[density ]

1.307±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

powder to crystal
[pka]

-2.82±0.50(Predicted)
[color ]

White to Orange to Green
[InChI]

1S/C20H18BrN/c1-15-3-9-18(10-4-15)22(19-11-5-16(2)6-12-19)20-13-7-17(21)8-14-20/h3-14H,1-2H3
[InChIKey]

YMNJJMJHTXGFOR-UHFFFAOYSA-N
[SMILES]

Cc1ccc(cc1)N(c2ccc(C)cc2)c3ccc(Br)cc3
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22-36/37/38
[Safety Statements ]

26
[WGK Germany ]

3
[HS Code ]

29214200
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Chemical Properties]

off-white powder
[Synthesis]

4,4'-Dimethyltriphenylamine

20440-95-3

4-Bromo-4',4''-dimethyltriphenylamine

58047-42-0

General procedure for the synthesis of 4-bromo-4',4''-dimethyltriphenylamine from 4,4'-dimethyltriphenylamine: 4,4'-dimethyltriphenylamine (10 g, 36.6 mmol) was dissolved in dichloromethane (200 mL) at room temperature, followed by the addition of N-bromosuccinimide (NBS) (6.764 g, 38 mmol). The reaction mixture was stirred for about 3 hours. Upon completion of the reaction, the solid insoluble material was removed by filtration and the filtrate was purified by passing through a silica gel column and subjected to fast column chromatography using a gradient elution (hexane to hexane/dichloromethane = 4:1). The fraction containing the target product was collected and concentrated under reduced pressure to remove the solvent to afford the white solid product 4-bromo-4',4''-dimethyltriphenylamine (compound 25) (12.86 g, 99.7% yield).

[References]

[1] Patent: US9172051, 2015, B2. Location in patent: Page/Page column 97; 98; 101; 102
[2] Patent: JP5966736, 2016, B2. Location in patent: Paragraph 0075; 0079
[3] Patent: WO2013/8951, 2013, A1. Location in patent: Page/Page column 31
Spectrum DetailBack Directory
[Spectrum Detail]

4-Bromo-4',4''-dimethyltriphenylamine(58047-42-0)1HNMR
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