Basic information Safety Supplier Related

2-(2-AMINOPHENYL)PROPAN-2-OL

Basic information Safety Supplier Related

2-(2-AMINOPHENYL)PROPAN-2-OL Basic information

Product Name:
2-(2-AMINOPHENYL)PROPAN-2-OL
Synonyms:
  • o-aminophenyldimethylcarbinol
  • Nsc76547
  • 2-Amino-alpha,alpha-dimethylbenzenemethanol
  • alhpa,alpha-Dimethyl-2-aminobenzyl alcohol
  • alpha,alpha-Dimethyl-o-aminobenzyl alcohol
  • o-Amino-alpha,alpha-dimethylbenzyl alcohol
  • 2-AMINO-ALPHA,ALPHA-DIMETHYLBENZYL ALCOHOL
  • 2-(2-AMINOPHENYL)PROPAN-2-OL
CAS:
15833-00-8
MF:
C9H13NO
MW:
151.21
Product Categories:
  • Benzhydrols, Benzyl & Special Alcohols
Mol File:
15833-00-8.mol
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2-(2-AMINOPHENYL)PROPAN-2-OL Chemical Properties

Boiling point:
289℃
Density 
1.084
Flash point:
129℃
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
pka
14.35±0.29(Predicted)
Appearance
Colorless to light yellow Viscous Liquid
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Safety Information

HazardClass 
IRRITANT
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2-(2-AMINOPHENYL)PROPAN-2-OL Usage And Synthesis

Synthesis

75-16-1

551-93-9

15833-00-8

GENERAL STEPS: 1-(2-aminophenyl)ethanone (1.50 g, 11.1 mmol) was dissolved in tetrahydrofuran (11 mL) under argon protection and cooled at 0 °C. Subsequently, methylmagnesium bromide (1.0 mol/L tetrahydrofuran solution, 11.1 mL, 11.1 mmol) was added slowly. After addition, the reaction mixture was gradually warmed to room temperature and stirred. Upon completion of the reaction, the reaction was carefully quenched with saturated aqueous ammonium chloride solution. The reaction mixture was extracted with ethyl acetate (3 x 20 mL), the organic phases were combined, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The crude product obtained was a brown oil, which was purified by fast column chromatography to give 2-(2-aminophenyl)propan-2-ol as a light-colored oil (1.20 g, 72% yield).LC-MS analysis showed a retention time of 0.24 min, and m/z 134 ([M-OH]-) was observed in ESI+ mode.1H NMR (400 MHz, chloroform-d) δ ( ppm): 7.15 (d, 1H), 7.06 (t, 1H), 6.72 (t, 1H), 6.65 (d, 1H), 3.65 (br s, 1H), 1.67 (s, 6H).

References

[1] Patent: WO2018/17490, 2018, A1. Location in patent: Paragraph 0163; 0164
[2] Bioorganic and Medicinal Chemistry Letters, 2007, vol. 17, # 1, p. 189 - 192
[3] Organic and Biomolecular Chemistry, 2015, vol. 13, # 47, p. 11486 - 11491

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