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ChemicalBook--->CAS DataBase List--->136630-36-9

136630-36-9

136630-36-9 Structure

136630-36-9 Structure
IdentificationBack Directory
[Name]

4,4'-dibroMobiphenyl-2,2'-diaMine
[CAS]

136630-36-9
[Synonyms]

DBDABP
4,4'-Dibromo-[1,1'-bipheny
2,2′-Diamino-4,4′-dibromobiphenyl
4,4′-Dibromo-2,2′-biphenyldiamine
4,4'-dibroMobiphenyl-2,2'-diaMine
2,2'-DiaMino-4,4'-dibroModiphenyl
4,4'-Dibromo-2,2'-diaminobiphenyl
4.4'-Dibrom-2.2'-diamino-diphenyl
4,4'-Dibromo-2,2'-biphenyldiamine 97%
2-(2-amino-4-bromophenyl)-5-bromoaniline
4,4'-Dibromo-[1,1'-biphenyl]-2,2'-diamine
[1,1'-Biphenyl]-2,2'-diamine, 4,4'-dibromo-
[Molecular Formula]

C12H10Br2N2
[MDL Number]

MFCD14582981
[MOL File]

136630-36-9.mol
[Molecular Weight]

342.03
Chemical PropertiesBack Directory
[Melting point ]

192-194℃
[Boiling point ]

436.5±40.0 °C(Predicted)
[density ]

1.784±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[form ]

solid
[pka]

2.79±0.10(Predicted)
[Appearance]

White to light yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS05,GHS07,GHS09
[Signal word ]

Danger
[Hazard statements ]

H302-H315-H318-H335-H400
[Precautionary statements ]

P273-P280-P301+P312+P330-P302+P352-P305+P351+P338+P310
[Hazard Codes ]

Xn,N
[Risk Statements ]

22-37/38-41-50/53
[Safety Statements ]

26-39-60-61
[RIDADR ]

UN 3077 9 / PGIII
[WGK Germany ]

3
Spectrum DetailBack Directory
[Spectrum Detail]

4,4'-dibroMobiphenyl-2,2'-diaMine(136630-36-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

4,4'-dibroMo-2,2'-dinitrobiphenyl

91371-12-9

4,4'-dibroMobiphenyl-2,2'-diaMine

136630-36-9

General procedure for the synthesis of 4,4'-dibromo-2,2'-dinitrobiphenyl-2,2'-diamine from 4,4'-dibromo-2,2'-dinitrobiphenyl: (2) Under nitrogen protection, 4,4'-dibromo-2,2'-dinitrobiphenyl (4.02 g, 10 mmol) was dissolved in a mixture of 48 mL of ethanol and 30 mL of water and tin powder (5.94 g, 50 mmol). The reaction mixture was then heated to 80 °C and maintained at 70 °C for 1 hour. Upon completion of the reaction, the heating was stopped and the reaction flask was cooled in an ice water bath. A 2 mol/L aqueous sodium hydroxide solution was slowly added dropwise until the pH of the reaction system was basic. Then extraction was carried out with dichloromethane, and the organic phases were combined and dried with anhydrous sodium sulfate. The product was purified by silica gel column chromatography using petroleum ether and tetrahydrofuran (20:1, v/v) as eluents. After removal of the solvent under reduced pressure, a light gray solid product was obtained in 85% yield. The structure of the product was confirmed by 1H NMR and confirmed as 4,4'-dibromobiphenyl-2,2'-diamine.

[References]

[1] Journal of Materials Chemistry A, 2016, vol. 4, # 22, p. 8750 - 8754
[2] Journal of Organic Chemistry, 1991, vol. 56, # 21, p. 6248 - 6250
[3] Journal of the American Chemical Society, 2006, vol. 128, # 28, p. 9034 - 9035
[4] Journal of Materials Chemistry, 2011, vol. 21, # 32, p. 11800 - 11814
[5] Molecular Crystals and Liquid Crystals, 2006, vol. 459, # 1, p. 85/[365]-94/[374]
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