Basic information Safety Supplier Related

2-FLUORO-6-HYDROXYBENZALDEHYDE

Basic information Safety Supplier Related

2-FLUORO-6-HYDROXYBENZALDEHYDE Basic information

Product Name:
2-FLUORO-6-HYDROXYBENZALDEHYDE
Synonyms:
  • 2-FLUORO-6-HYDROXYBENZALDEHYDE
  • 6-FLUOROSALICYLALDEHYDE
  • 6-Fluorosalicylaldehyde,97%
  • 2-Fluoro-6-hydroxybenzaldehyde 98%
  • 6-Fluorosalicylaldehyde, 3-Fluoro-2-formylphenol
  • 2-Fluor-6-Hydroxybenzaldehyde
  • 6-Fluorosalicylaldehyde>
  • Benzaldehyde, 2-fluoro-6-hydroxy-
CAS:
38226-10-7
MF:
C7H5FO2
MW:
140.11
EINECS:
642-482-0
Product Categories:
  • Aromatic Aldehydes & Derivatives (substituted)
  • Aromatics
  • Inhibitors
Mol File:
38226-10-7.mol
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2-FLUORO-6-HYDROXYBENZALDEHYDE Chemical Properties

Melting point:
37-39°C
Boiling point:
201.3±20.0 °C(Predicted)
Density 
1.350±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
powder to lump
pka
7.18±0.10(Predicted)
color 
White to Yellow to Orange
Sensitive 
Air Sensitive
BRN 
1935289
InChI
InChI=1S/C7H5FO2/c8-6-2-1-3-7(10)5(6)4-9/h1-4,10H
InChIKey
FZIBGCDUHZBOLA-UHFFFAOYSA-N
SMILES
C(=O)C1=C(O)C=CC=C1F
CAS DataBase Reference
38226-10-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36-36/37/39-27
Hazard Note 
Irritant
HS Code 
2912490090

MSDS

  • Language:English Provider:ALFA
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2-FLUORO-6-HYDROXYBENZALDEHYDE Usage And Synthesis

Uses

2-FLUORO-6-HYDROXYBENZALDEHYDE is used in the preparation of aromatic compounds as human PAI-1 inhibitors.

Synthesis

199388-02-8

38226-10-7

Step 3: Synthesis of 2-fluoro-6-hydroxybenzaldehyde A solution of 2-fluoro-6-((tetrahydro-2H-pyran-2-yl)oxy)benzaldehyde (6.5 g, 29.0 mmol) and p-toluenesulfonic acid (TsOH, 2 g, 11.6 mmol) in dichloromethane (DCM, 30 mL) was stirred for 5 hours at room temperature. After completion of the reaction, the mixture was diluted with dichloromethane (100 mL). The organic layer was washed sequentially with saturated aqueous sodium bicarbonate and brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography (eluent: petroleum ether/ethyl acetate = 100:1 to 20:1 gradient elution) to afford 2-fluoro-6-hydroxybenzaldehyde (3.0 g, 74% yield) as a light yellow solid. 1H NMR (400 MHz, CDCl3): δ 11.49 (s, 1H), 10.29 (s, 1H), 7.46-7.52 (m, 1H), 6.79 (d, J = 8.8 Hz, 1H), 6.63-6.68 (m, 1H).

References

[1] Journal of the Chemical Society - Perkin Transactions 1, 1997, # 19, p. 2925 - 2929
[2] Patent: US2017/37038, 2017, A1. Location in patent: Paragraph 0096; 0378; 0382; 0383

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