3,5-DIIODO-4-HYDROXYBENZALDEHYDE
3,5-DIIODO-4-HYDROXYBENZALDEHYDE Basic information
- Product Name:
- 3,5-DIIODO-4-HYDROXYBENZALDEHYDE
- Synonyms:
-
- AKOS B028744
- 3,5-DIIODO-4-HYDROXYBENZALDEHYDE
- 4-HYDROXY-3,5-DIIODO-BENZALDEHYDE
- 3,5-Diiodo-4-Hydroxybenzaldhyde
- 3,5-DIIODO-4-HYDROXYBENZALDEHYDE, 98+%
- Levothyroxine Sodium Impurity f
- 2,6-Diiodo-4-formylphenol
- NSC 72943
- CAS:
- 1948-40-9
- MF:
- C7H4I2O2
- MW:
- 373.91
- EINECS:
- 217-754-3
- Product Categories:
-
- Aromatic Aldehydes & Derivatives (substituted)
- Aromatics
- Miscellaneous Reagents
- Mol File:
- 1948-40-9.mol
3,5-DIIODO-4-HYDROXYBENZALDEHYDE Chemical Properties
- Melting point:
- 202-203°C
- Boiling point:
- 284.1±40.0 °C(Predicted)
- Density
- 2.602±0.06 g/cm3(Predicted)
- storage temp.
- -20°C Freezer, Under Inert Atmosphere
- solubility
- Chloroform (Slightly, Sonicated), DMSO (Slightly)
- form
- Solid
- pka
- 4.89±0.23(Predicted)
- color
- White to Pale Yellow
- Water Solubility
- Insoluble in water. Sparingly soluble in chloroform and methanol.
- Sensitive
- Air & Light Sensitive
- BRN
- 1283414
- InChI
- InChI=1S/C7H4I2O2/c8-5-1-4(3-10)2-6(9)7(5)11/h1-3,11H
- InChIKey
- WHLUEIMENHLCMY-UHFFFAOYSA-N
- SMILES
- C(=O)C1=CC(I)=C(O)C(I)=C1
- CAS DataBase Reference
- 1948-40-9(CAS DataBase Reference)
MSDS
- Language:English Provider:ALFA
3,5-DIIODO-4-HYDROXYBENZALDEHYDE Usage And Synthesis
Chemical Properties
Pale Beige Solid
Uses
3,5-Diiodo-4-hydroxybenzaldehyde (cas# 1948-40-9) is a compound useful in organic synthesis.
Synthesis
3,5-Diiodo-4-hydroxybenzaldehyde was prepared as follows: in a 100 mL round bottom flask, 4-hydroxybenzaldehyde (1.0 g, 8.19 mmol), sodium periodate (1.75 g, 8.19 mmol), and NaCl (957 mg, 16.38 mmol) were dissolved in acetic acid (30 mL). H2O (3 mL) was added at room temperature. The reaction mixture was stirred at room temperature for 10 min, then potassium iodide (2.72 g, 16.4 mmol) was added and the reaction mixture was stirred at room temperature for 96 hours. The reaction mixture was diluted with EtOAc (25 mL) and 1 M aqueous sodium thiosulfate. The solution (25 mL) was added and the resulting mixture was stirred for 15 minutes. The solution was poured into 250 mLErlenmeyer and washed with EtOAc (50 mL) and 1 M aqueous sodium thiosulfate. solution (50mL) and the resulting solution was stirred for another 15 minutes. The organic layer was separated and the aqueous phase was further extracted with EtOAc (3 x 50 mL). The combined organic layers were washed with brine (100 mL), dried over Na2SO4, filtered and concentrated to dryness to afford 4-hydroxy-3,5-diiodobenzaldehyde (2.91 g, 95% yield) as a light yellow solid.
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3,5-DIIODO-4-HYDROXYBENZALDEHYDE(1948-40-9)Related Product Information
- 3,5-DIIODO-4-HYDROXYBENZALDEHYDE
- BENZIODARONE
- 3,5-DIIODO-4-HYDROXYBENZOIC ACID
- Desethylamiodarone
- furidarone
- Amiodarone
- Acetiromate
- Amiodarone hydrochloride
- 3,5-DIIODO-2-HYDROXYBENZALDEHYDE,3 5-DIIODO-2-HYDROXYBENZALDEHYDE 95%
- 3,5-DIIODO-4-METHOXYBENZHYDRAZIDE
- 3-(3,5-DIIODO-4-HYDROXYBENZOYL)-INDOLE
- 3,5-DIIODO-4-HYDROXYBENZHYDRAZIDE
- 4-(4'-HYDROXY-3'-IODOPHENOXY)-3,5-DIIODO-BENZOIC ACID
- 3,5-DIIODO-4(4'-METHOXYPHENOXY)BENZOIC ACID
- 3,5-DIIODO-4(4'-METHOXYPHENOXY)BENZOIC ACID METHYL ESTER
- 3,5-DIIODO-4'-(4-HYDROXYPHENOXY)BENZOIC ACID
- METHYL 3,5-DIIODO-4-METHOXYBENZOATE
- 3,5,3',5'-TETRAIODOTHYROFORMIC ACID