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121-27-7

121-27-7 Structure

121-27-7 Structure
IdentificationMore
[Name]

2-AMINO-4,4'-DICHLORODIPHENYL ETHER
[CAS]

121-27-7
[Synonyms]

2-AMINO-4,4'-DICHLORODIPHENYL ETHER
5-CHLORO-2-(4-CHLOROPHENOXY)ANILINE
AURORA KA-6780
5-chloro-2-(4-chlorophenoxy)-benzenamin
5-chloro-2-(4-chlorophenoxy)-Benzenamine
Benzenamine,5-chloro-2-(4-chlorophenoxy)-
5-Chloro-2-(4-Clorophenoxy)Aniline
C.I.Azoic Diazo Component 33
Diazo Fast Red FR
Fast Red FR Base
Fast Red Salt FRN.
C.I.37075(base)
C.I.Azoic Diazo Component 33(base)
[EINECS(EC#)]

204-460-5
[Molecular Formula]

C12H9Cl2NO
[MDL Number]

MFCD00027391
[Molecular Weight]

254.11
[MOL File]

121-27-7.mol
Chemical PropertiesBack Directory
[Melting point ]

61.0 to 65.0 °C
[Boiling point ]

234°C/27mmHg(lit.)
[density ]

1.364±0.06 g/cm3(Predicted)
[storage temp. ]

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

powder to crystal
[pka]

2.99±0.10(Predicted)
[color ]

White to Yellow to Orange
[CAS DataBase Reference]

121-27-7(CAS DataBase Reference)
[EPA Substance Registry System]

4,4'-Dichloro-2-aminodiphenyl ether (121-27-7)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

2922290090
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Nitrogen-->Formic acid-->4-Chloro-1-(4-chlorophenoxy)-2-nitrobenzene-->4-Chlorophenol-->2,5-Dichloronitrobenzene-->1,4-Dichlorobenzene-->Acetic acid-->Ferric chloride-->Hydrazine hydrate
[Preparation Products]

244TRICHLORODIPHENYLETHER
Hazard InformationBack Directory
[Chemical Properties]

Brown solid
[Synthesis]

4-Chloro-1-(4-chlorophenoxy)-2-nitrobenzene

135-12-6

2-AMINO-4,4'-DICHLORODIPHENYL ETHER

121-27-7

4,4'-Dichloro-2-nitro-diphenyl ether (12.0 g, 42.2 mmol) was used as a raw material, which was mixed with FeCl3 (702 mg, 4.33 mmol) and activated charcoal (3.70 g) in MeOH (360 mL) and stirred at 50 °C. Hydrazine monohydrate (7.00 mL, 144 mmol) was added slowly over 10 minutes, followed by heating the reaction mixture to reflux and stirring for 1 hour. After completion of the reaction, the mixture was cooled, filtered through diatomaceous earth and the filter cake was washed with MeOH. The filtrate was concentrated under reduced pressure to give an oily residue. This residue was dissolved with EtOAc, and the organic layer was washed sequentially with saturated aqueous NaHCO3 and brine, and then dried with Na2SO4. After filtration to remove the insoluble matter, the filtrate was concentrated under reduced pressure to give 5-chloro-2-(4-chlorophenoxy)-aniline (8) (10.6 g, 99% yield) as a colorless solid with a melting point of 59-61 °C. The product was characterized by 1H NMR (400 MHz, CDCl3), 13C NMR (100 MHz, CDCl3) and LC-MS (ESI) to confirm its structure.

[References]

[1] Bioorganic and Medicinal Chemistry, 2015, vol. 23, # 15, p. 4952 - 4969
[2] Patent: CN107353185, 2017, A. Location in patent: Paragraph 0031; 0034; 0036
[3] Journal of the Chemical Society, 1929, p. 521
[4] Journal of the Chemical Society, 1931, p. 529,533
[5] Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 9, p. 323
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