2-Fluoro-4-hydroxybenzaldehyde
2-Fluoro-4-hydroxybenzaldehyde Basic information
- Product Name:
- 2-Fluoro-4-hydroxybenzaldehyde
- Synonyms:
-
- 2-FLUORO-4-HYDROXYBENZALDEHYDE
- 2-FLURO-4-HYDROXYBENZALDEHYDE
- 2-Fluoro-4-hydroxybenzaldehyde,98%
- 3-Fluoro-4-formylphenol
- Benzaldehyde, 2-fluoro-4-hydroxy-
- 2-Fluoro-6-nitroacetophenone
- CAS:
- 348-27-6
- MF:
- C7H5FO2
- MW:
- 140.11
- Product Categories:
-
- Aromatic Aldehydes & Derivatives (substituted)
- API intermediates
- Mol File:
- 348-27-6.mol
2-Fluoro-4-hydroxybenzaldehyde Chemical Properties
- Melting point:
- 168-170°C
- Boiling point:
- 254.2±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
- crystalline powder
- pka
- 6.78±0.18(Predicted)
- color
- Light tan
- InChI
- InChI=1S/C7H5FO2/c8-7-3-6(10)2-1-5(7)4-9/h1-4,10H
- InChIKey
- ONRPXRPUBXXCCM-UHFFFAOYSA-N
- SMILES
- C(=O)C1=CC=C(O)C=C1F
- CAS DataBase Reference
- 348-27-6(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi,Xn
- Risk Statements
- 22-37/38-41-52
- Safety Statements
- 26-39
- Hazard Note
- Irritant
- HS Code
- 2912490090
2-Fluoro-4-hydroxybenzaldehyde Usage And Synthesis
Uses
2-Fluoro-4-hydroxybenzaldehyde is a useful reagent for preparation of 3,4-ring fused 7-azaindoles and deazapurines as potent JAK2 inhibitors.
Uses
2-Fluoro-4-hydroxybenzaldehyde is mainly used as an intermediate for physiologically active compounds such as pharmaceuticals or pesticides and is a wide range of organic building blocks. Its structure contains fluorine, aldehyde groups, and phenolic hydroxyl groups, and these groups can add or replace other functional groups.
Synthesis
Preparation of 2-fluoro-4-hydroxybenzaldehyde involves: (1) mixing 3-fluorophenol (I), potassium carbonate, and 2-bromopropane in an organic solvent, and heating to react to obtain 1-fluoro-3-isopropoxybenzene (II); (2) dissolving compound (II) in an organic solvent and reacting with a brominating reagent to obtain 1-bromo-2-fluoro-4-isopropoxybenzene (III); (3) dissolving compound (III) in tetrahydrofuran, dripping isopropylmagnesium chloride/tetrahydrofuran solution at -10°C to 0°C, adding dimethylformamide to react after Grignard exchange to obtain 2-fluoro-4-isopropoxybenzaldehyde (IV); and (4) reacting compound (IV) with boron trichloride and deprotecting.
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2-Fluoro-4-hydroxybenzaldehyde(348-27-6)Related Product Information
- 4-Hydroxybenzaldehyde
- Benzaldehyde
- Salicylaldehyde
- 3-(Trifluoromethyl)benzaldehyde
- 2-(Trifluoromethyl)benzaldehyde
- 3-Hydroxybenzaldehyde
- 2-Fluoro-4-hydroxybenzoic acid
- 2-Fluoro-4-methylbenzoic acid
- 3-FLUORO-4-HYDROXYBENZALDEHYDE
- Fluorine
- 2-Fluoro-4-methoxyacetophenone
- 2,3,5,6-Tetrafluoro-4-hydroxy-benzoic acid
- 2'-Fluoro-4'-hydroxyacetophenone
- 6-FLUOROVERATRALDEHYDE
- 3-FLUORO-2-HYDROXYBENZALDEHYDE,3-Fluoro-2-Hydroxybenzaldehyde 3-Fluoro Salicylaldehyde,3-Fluoro-2-hydroxybenzaldehyde ,99%
- 2-FLUORO-5-HYDROXYBENZALDEHYDE
- 5-Fluorosalicylaldehyde
- 3,5-Difluoro-4-hydroxybenzaldehyde