2-HYDROXY-1,3,5-BENZENETRICARBALDEHYDE
2-HYDROXY-1,3,5-BENZENETRICARBALDEHYDE Basic information
- Product Name:
- 2-HYDROXY-1,3,5-BENZENETRICARBALDEHYDE
- Synonyms:
-
- 2-HYDROXY-1,3,5-BENZENETRICARBALDEHYDE
- 2-Hydroxybenzene-1,3,5-tricarbaldehyde
- 2-HYDROXYBENZENE-1,3,5-TRICARBOXALDEHYDE
- 1,3,5-Benzenetricarboxaldehyde,2-hydroxy-|||
- 1,3,5-Benzenetricarboxaldehyd
- 2-Hydroxy-1,3,5-benzenetricarboxaldehyde
- 2-hydroxy-1,3,5-triformylbenzene
- 2-hydroxy-1,3,5-benzenetrialdehyde
- CAS:
- 81502-74-1
- MF:
- C9H6O4
- MW:
- 178.14
- Mol File:
- 81502-74-1.mol
2-HYDROXY-1,3,5-BENZENETRICARBALDEHYDE Chemical Properties
- Melting point:
- 179 °C
- Boiling point:
- 282.9±40.0 °C(Predicted)
- Density
- 1.449±0.06 g/cm3(Predicted)
- storage temp.
- Inert atmosphere,Room Temperature
- form
- powder to crystal
- pka
- 4.20±0.23(Predicted)
- color
- White to Yellow
- λmax
- 335nm(EtOH)(lit.)
2-HYDROXY-1,3,5-BENZENETRICARBALDEHYDE Usage And Synthesis
Chemical Properties
2-Hydroxy- 1,3,5-benzenetricarbaldehyde has a very limited solubility in most organic solvents and in water. It dissolves well in DMSO and in hot DMF, and the latter can be used as a recrystallization solvent. While the trialdehyde 3 is colorless in its free acid form, its anion absorbs light in the visible region giving the compound a yellow coloration in solutions when dissociation can occur. The yellow sodium salt of 2-hydroxy- 1,3,5-benzenetricarbaldehyde is only slightly soluble in water.
Synthesis
2-Hydroxybenzene-1,3,5-tricarbaldehyde is synthesized from phenol or 4-hydroxybenzaldehyde[1].
References
[1] A. ANDERSON. A Convenient One-Step Synthesis of 2-Hydroxy-1,3,5-Benzenetricarbaldehyde[J]. Synthetic Communications, 2000. DOI:10.1080/00397910008086933.
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