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2-AMINO-3-FLUOROPHENOL

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2-AMINO-3-FLUOROPHENOL Basic information

Product Name:
2-AMINO-3-FLUOROPHENOL
Synonyms:
  • 6-Fluoro-2-hydroxyaniline
  • 2-AMINO-3-FLUOROPHENOL
  • Phenol, 2-aMino-3-fluoro-
  • 2-Fluoro-6-hydroxyaniline
  • 2-AMINO-3-FLUOROPHENOL ISO 9001:2015 REACH
CAS:
53981-23-0
MF:
C6H6FNO
MW:
127.12
Product Categories:
  • Fluorine series
Mol File:
53981-23-0.mol
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2-AMINO-3-FLUOROPHENOL Chemical Properties

Melting point:
126-127°
Boiling point:
221.9±25.0 °C(Predicted)
Density 
1.347±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
form 
solid
pka
8.76±0.10(Predicted)
color 
Light yellow to brown
InChI
InChI=1S/C6H6FNO/c7-4-2-1-3-5(9)6(4)8/h1-3,9H,8H2
InChIKey
QOZLOYKAFDTQNU-UHFFFAOYSA-N
SMILES
C1(O)=CC=CC(F)=C1N
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
22-37/38-41
Safety Statements 
26-39
RIDADR 
2512
HazardClass 
IRRITANT
PackingGroup 
HS Code 
2908990000
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2-AMINO-3-FLUOROPHENOL Usage And Synthesis

Uses

2-Amino-3-fluorophenol is a reagent that is used in the preparation of benzimidazole- and benzoxazole-pyrimidone selective PI3Kβ inhibitors for the treatment of phosphatase and TENsin homologue (PTEN) deficient cancers.

Synthesis

385-01-3

53981-23-0

Step 1. General procedure for the synthesis of 2-amino-3-fluorophenol from 3-fluoro-2-nitrophenol: Stannous chloride dihydrate (0.724 g, 3.18 mmol) was added to a solution of tetrahydrofuran (THF, 5.0 mL) of 3-fluoro-2-nitrophenol (0.100 g, 0.636 mmol, SynQuest), followed by water ( 5.0 mL). The reaction mixture was heated to 80 °C and maintained for 40 min. After the reaction was completed, it was cooled to room temperature and the reaction mixture was diluted with ethyl acetate and saturated sodium bicarbonate solution. The insoluble material was removed by filtration and the organic and aqueous layers were separated. The aqueous layer was extracted three times with ethyl acetate. The combined organic extracts were washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated to give the crude product 2-amino-3-fluorophenol (65 mg, 80% yield), which could be used in the subsequent reaction without further purification.LCMS (M + H)+: 128.0.

References

[1] ChemMedChem, 2017, vol. 12, # 17, p. 1436 - 1448
[2] Journal of Labelled Compounds and Radiopharmaceuticals, 2006, vol. 49, # 7, p. 623 - 634
[3] Patent: US5886044, 1999, A
[4] Patent: US5780483, 1998, A
[5] Patent: US6262113, 2001, B1

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