ChemicalBook--->CAS DataBase List--->3096-69-3

3096-69-3

3096-69-3 Structure

3096-69-3 Structure
IdentificationBack Directory
[Name]

4-AMINO-2,3-XYLENOL
[CAS]

3096-69-3
[Synonyms]

4-AMINO-2,3-XYLENOL
4-AMINO-2,3-XYLENOL 97+%
2,3-DIMETHYL-4-AMINOPHENOL
4-amino-2,3-dimethylphenol
4-azanyl-2,3-dimethyl-phenol
4-hydroxy-2,3-dimethylaniline
4-Amino-2,3-dimethylphenol 4-Hydroxy-2,3-dimethylaniline
[EINECS(EC#)]

221-446-4
[Molecular Formula]

C8H11NO
[MDL Number]

MFCD00070554
[MOL File]

3096-69-3.mol
[Molecular Weight]

137.18
Chemical PropertiesBack Directory
[Melting point ]

174°C
[Boiling point ]

296.3±28.0 °C(Predicted)
[density ]

1.118±0.06 g/cm3(Predicted)
[storage temp. ]

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

soluble in Methanol
[form ]

powder to crystal
[pka]

10.70±0.23(Predicted)
[color ]

White to Gray to Brown
[CAS DataBase Reference]

3096-69-3
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
[Risk Statements ]

20/21/22-36/37/38
[Safety Statements ]

26-36/37/39
[HS Code ]

2922.29.8190
Spectrum DetailBack Directory
[Spectrum Detail]

4-AMINO-2,3-XYLENOL(3096-69-3)MS
4-AMINO-2,3-XYLENOL(3096-69-3)IR1
4-AMINO-2,3-XYLENOL(3096-69-3)IR2
Hazard InformationBack Directory
[Synthesis]

2,3-DIMETHYL-4-NITROPHENOL

19499-93-5

4-AMINO-2,3-XYLENOL

3096-69-3

General procedure for the synthesis of 4-amino-2,3-xylenol from 2,3-dimethyl-4-nitrophenol: A mixture of 2,3-dimethyl-4-nitrophenol (2 g, 1.2 mmol) with 10% Pd/C catalyst (1.83 g) in ethanol (80 mL) was placed under hydrogen atmosphere and reacted with stirring at room temperature for 5 hours. Upon completion of the reaction, the crude reaction mixture was filtered through diatomaceous earth and the filter cake was washed with dichloromethane (DCM). After evaporation to remove the solvent, 4-amino-2,3-xylenol (1.60 g, 97% yield) was obtained as a brown powder. The product was characterized by 1H-NMR (DMSO-d6): δ 1.94 (s, 3H, methyl proton), 2.01 (s, 3H, methyl proton), 4.06 (s, 2H, amino proton), 6.32 (d, 1H, aromatic proton H-6, J = 8.1 Hz), 6.40 (d, 1H, aromatic proton H-5, J = 8.1 Hz), 6.61 (s , 1H, aromatic proton H-2), 8.10 (broad s, 1H, hydroxyl proton).

[References]

[1] Patent: WO2006/43090, 2006, A1. Location in patent: Page/Page column 176
[2] Journal of Medicinal Chemistry, 2009, vol. 52, # 13, p. 3881 - 3891
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