ChemicalBook--->CAS DataBase List--->24878-25-9

24878-25-9

24878-25-9 Structure

24878-25-9 Structure
IdentificationBack Directory
[Name]

2,2'-OXYDIANILINE
[CAS]

24878-25-9
[Synonyms]

2,2'-OXYDIANILINE
2,2’-Oxydlaniline
2-AMINOPHENYL ETHER
2,2'-OXYDIANILINE
Aniline, 2,2'-oxydi-
Olanzapine Impurity 33
2,2'-Oxybis(benzenamine)
Bis(2-aminophenyl) ether
2-(2-aminophenoxy)aniline
Benzenamine, 2,2'-oxybis-
2,2'-Diaminodiphenyl ether
2,2'-OXYDIANILINE in stock Factory
2,2′-Oxydianiline,2-Aminophenyl ether
[Molecular Formula]

C12H12N2O
[MDL Number]

MFCD00792533
[MOL File]

24878-25-9.mol
[Molecular Weight]

200.24
Chemical PropertiesBack Directory
[Melting point ]

61-64 °C(lit.)
[Boiling point ]

148.5-149.5 °C(Press: 0.3 Torr)
[density ]

1.216
[storage temp. ]

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

Powder
[pka]

4.15±0.10(Predicted)
[color ]

White to pale brown
[Water Solubility ]

Slightly soluble in water.
[InChI]

InChI=1S/C12H12N2O/c13-9-5-1-3-7-11(9)15-12-8-4-2-6-10(12)14/h1-8H,13-14H2
[InChIKey]

GOJFAKBEASOYNM-UHFFFAOYSA-N
[SMILES]

O(C1=CC=CC=C1N)C1=CC=CC=C1N
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-27-36/37/39-45
[WGK Germany ]

3
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Uses]

It is catalytic reagent and used in pharmaceutical industry.
[Synthesis]

2,2'-Oxybis(nitrobenzene)

2217-65-4

2,2'-OXYDIANILINE

24878-25-9

General procedure for the synthesis of 2,2'-diaminodiphenyl ether from 2,2'-oxo-bis(nitrobenzene): first, an aqueous suspension of iron powder and hydrochloric acid was refluxed under stirring for 25 minutes. Subsequently, the corresponding dinitro compound was added to this hot suspension and the reflux reaction was continued for 24 hours. Upon completion of the reaction, the mixture was cooled to room temperature and hydrolyzed with 20 mL of 2.5 M sodium hydroxide solution. Next, the reaction mixture was extracted with chloroform (20 mL each time, twice). The organic phases were combined, dried with anhydrous sodium sulfate and finally the solvent was evaporated to give the target product 2,2'-diaminodiphenyl ether as a solid.

[References]

[1] Tetrahedron, 1995, vol. 51, # 2, p. 579 - 590
[2] Polyhedron, 2015, vol. 90, p. 165 - 174
[3] Synthesis, 1996, # 8, p. 930 - 940
[4] Journal of Organic Chemistry, 1994, vol. 59, # 24, p. 7306 - 7315
[5] Zeitschrift fur Anorganische und Allgemeine Chemie, 2015, vol. 641, # 1, p. 128 - 135
Spectrum DetailBack Directory
[Spectrum Detail]

2,2'-OXYDIANILINE(24878-25-9)1HNMR
2,2'-OXYDIANILINE(24878-25-9)IR
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