产品名称
2,6-二甲酰-4-甲基苯酚, 97%
InChI key
ZBOUXALQDLLARY-UHFFFAOYSA-N
InChI
1S/C9H8O3/c1-6-2-7(4-10)9(12)8(3-6)5-11/h2-5,12H,1H3
SMILES string
Cc1cc(C=O)c(O)c(C=O)c1
assay
97%
form
solid
mp
128-130 °C (lit.)
functional group
aldehyde
Quality Level
Application
2-Hydroxy-5-methyl-1,3-benzenedicarboxaldehyde (2-hydroxy-5-methylisophthalaldehyde) is suitable reagent used in the synthesis of 2-(2′-vinyloxyethoxy)-5-methylisophthaldehyde and chiral calixsalen macrocycles.
2-Hydroxy-5-methyl-1,3-benzenedicarboxaldehyde may be used in the synthesis of the following:
2-Hydroxy-5-methyl-1,3-benzenedicarboxaldehyde may be used in the synthesis of the following:
- 3-[(2,4-Dichlorophenyl)iminomethyl]-2-hydroxy-5-methylbenzaldehyde, a Schiff base.
- 2-Hydroxy-3-methoxymethyl-5-methylbenzaldehyde.
- Acyclic Schiff-base ligands.
- Macrobicyclic ligands (MSB).
- 4-Methyl-2,6-divinylphenol.
- 2-Hydroxy-3-dimethoxymethyl-5-methylbenzaldehyde.
General description
2-Hydroxy-5-methyl-1,3-benzenedicarboxaldehyde (2-hydroxy-5-methylisophthalaldehyde) is a dialdehyde derivative. It has been synthesized by heating p-cresol with hexamethylenetetramine. The structure has been confirmed by 1H and 13C NMR. It is an important raw material for the synthesis of various binucleating schiff base ligand.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
3-[(2, 4-Dichlorophenyl) iminomethyl]-2-hydroxy-5-methylbenzaldehyde.
Kilic I, et al
Acta Crystallographica Section E, Structure Reports Online, 65(6), 1347-1347 (2009)
2-Hydroxy-3-methoxymethyl-5-methylbenzaldehyde.
Gunasekaran B, et al
Acta Crystallographica Section E, Structure Reports Online, 69(2), 317-317 (2013)
Steric effect in the free radical polymerization of vinyl ethers containing electron-deficient olefin groups.
Lee JY and Jin MK
Polymer Bull., 44(3), 2777-2284 (2000)
ESI MS, spectroscopic and semiempirical characterization of a macrobicyclic complex with Er (III) cation.
Przybylski P, et al.
Journal of Molecular Structure, 878(1), 95-103 (2008)
New efficient ruthenium metathesis catalyst containing chromenyl ligand.
Hryniewicka A, et al
Journal of Organometallic Chemistry, 695(9), 1265-1270 (2010)
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