ChemicalBook--->CAS DataBase List--->17802-36-7

17802-36-7

17802-36-7 Structure

17802-36-7 Structure
IdentificationMore
[Name]

3,4-Dimethyldiphenylamine
[CAS]

17802-36-7
[Synonyms]

3,4-Dimethyldiphenylamine
3,4-dimethyl-n-phenyl-benzenamine
Benzenamine,3,4-dimethyl-N-phenyl-
3,4imethyltriphenylamine
[EINECS(EC#)]

679-857-3
[Molecular Formula]

C14H15N
[MDL Number]

MFCD03093248
[Molecular Weight]

197.28
[MOL File]

17802-36-7.mol
Chemical PropertiesBack Directory
[Melting point ]

57°C
[Boiling point ]

333.3±11.0 °C(Predicted)
[density ]

1.049±0.06 g/cm3(Predicted)
[storage temp. ]

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

powder to crystal
[pka]

1.42±0.50(Predicted)
[color ]

White to Light yellow
[InChI]

InChI=1S/C14H15N/c1-11-8-9-14(10-12(11)2)15-13-6-4-3-5-7-13/h3-10,15H,1-2H3
[InChIKey]

ACWJKFBBRPYPLL-UHFFFAOYSA-N
[SMILES]

C1(NC2=CC=CC=C2)=CC=C(C)C(C)=C1
[CAS DataBase Reference]

17802-36-7(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
[HS Code ]

2921490090
Hazard InformationBack Directory
[Chemical Properties]

White crystalline
[Uses]

3,4-Dimethyldiphenylamine is mainly used in the synthesis of organic optoelectronic materials.
[Synthesis]

3,4-Dimethyldiphenylamine can be synthesised electrochemically. The synthesis procedure is as follows: To a 25 mL electrolytic cell, add 0.2 mmol of 3,4-dimethyldiphenylhydrazine, 0.2 mmol of hydrochloric acid, 0.4 mmol of lithium acetate, and 6 mL of N,N-dimethylacetamide. Under ambient conditions at room temperature, with continuous stirring using a magnetic stir bar, insert tin foil as both the anode and cathode into the cell and allow the reaction to proceed for 6 hours at a constant current of 12 mA, monitoring progress via TLC; Upon completion of the reaction, the reaction mixture was quenched with water, extracted with ethyl acetate, back-extracted with saturated saline solution, dried over anhydrous sodium sulphate, and subjected to reduced-pressure distillation at 45 °C. The residue was purified by rapid silica gel column chromatography (ethyl acetate: petroleum ether = 10:1) to obtain the product 3,4-dimethyldiphenylamine, with a yield of 93%.
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