| Identification | Back Directory | [Name]
3-Amino-2-methylphenol | [CAS]
53222-92-7 | [Synonyms]
3-AMINO-O-CRESOL
2-amino-o-cresol
3-Amino-o-cresol,95%
3-AMINO-2-METHYLPHENOL
3-Amino-o-cresol
2-Amino-6-hydroxytoluene
Phenol, 3-aMino-2-Methyl-
3-HYDROXY-2-METHYLANILINE
2-METHYL-3-HYDROXY ANILINE
3-AMino-o-cresol , 98.0%(T)
3-Amino-2-methylphenol,3-Amino-o-cresol
3-Amino-2-methylphenol
3-Hydroxy-2-methylaniline | [EINECS(EC#)]
258-438-5 | [Molecular Formula]
C7H9NO | [MDL Number]
MFCD00007787 | [MOL File]
53222-92-7.mol | [Molecular Weight]
123.15 |
| Chemical Properties | Back Directory | [Appearance]
brown to black crystalline powder | [Melting point ]
129-130 °C(lit.)
| [Boiling point ]
229.26°C (rough estimate) | [density ]
1.0877 (rough estimate) | [refractive index ]
1.5380 (estimate) | [storage temp. ]
Keep in dark place,Inert atmosphere,Room temperature | [solubility ]
soluble in Methanol | [form ]
Solid | [pka]
10.36±0.10(Predicted) | [color ]
White to Gray to Brown | [InChI]
InChI=1S/C7H9NO/c1-5-6(8)3-2-4-7(5)9/h2-4,9H,8H2,1H3 | [InChIKey]
FLROJJGKUKLCAE-UHFFFAOYSA-N | [SMILES]
C1(O)=CC=CC(N)=C1C |
| Hazard Information | Back Directory | [Chemical Properties]
brown to black crystalline powder | [Uses]
3-Amino-2-methylphenol is used in production of (Diimido)dicarboxylic Acid, Imide, Polyamic Acid, Polyamides, Polyesters, and Polyureas. | [Synthesis]
The general procedure for the synthesis of 2-methyl-3-aminophenol from 2-methyl-3-nitrophenol was as follows: 2-methyl-3-nitrophenol (2.0 g, 13.1 mmol) was dissolved in methanol (50 mL) at room temperature, and 10 wt% palladium carbon catalyst (100 mg) was added. The reaction mixture was stirred under hydrogen atmosphere for 24 hours. Upon completion of the reaction, the palladium carbon catalyst was filtered through diatomaceous earth to remove the palladium carbon catalyst. The filtrate was concentrated under reduced pressure to afford the dark solid product 2-methyl-3-aminophenol (1.62 g, 99% yield). The product was analyzed by 1H NMR (CD3OD, δ=3.31 ppm, 400 MHz) showing: 6.77-6.73 (t, 1H), 6.29-6.27 (d, 1H), 6.22-6.20 (d, 1H), 2.02 (s, 3H). 13C NMR (CD3OD, δ=49.00 ppm, 100 MHz) analysis showed: 156.7,147.5,127.2,110.9,108.8,106.7,9.2. High-resolution mass spectrometry (HRMS-ESI) analysis showed that the calculated value of [M+H]+ (C7H10NO) was 124.0757 and the measured value was 124.0759. | [References]
[1] Patent: US5952362, 1999, A
[2] Patent: EP887346, 1998, A2
[3] European Journal of Medicinal Chemistry, 2017, vol. 125, p. 87 - 100
[4] Patent: KR2017/31307, 2017, A. Location in patent: Paragraph 0182-0184
[5] Journal of Medicinal Chemistry, 2010, vol. 53, # 5, p. 1964 - 1978 |
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