3,5-Dimethyl-4-hydroxybenzaldehyde
3,5-Dimethyl-4-hydroxybenzaldehyde structure
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Common Name | 3,5-Dimethyl-4-hydroxybenzaldehyde | ||
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| CAS Number | 2233-18-3 | Molecular Weight | 150.17 | |
| Density | 1.1±0.1 g/cm3 | Boiling Point | 263.9±35.0 °C at 760 mmHg | |
| Molecular Formula | C9H10O2 | Melting Point | 112-114 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 109.7±18.5 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Phase transfer catalyzed polymerization of 4-hydroxy-3, 5-dimethylbenzyl alcohol and copolymerization of 4-bromo-2, 6-dimethylphenol with 4-hydroxy-3, 5-dimethylbenzyl alcohol. Wang JH and Percec V.
Polym. Bull. 25(1) , 25-32, (1991)
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Structure-mechanism relationships in hemoproteins. Oxygenations catalyzed by chloroperoxidase and horseradish peroxidase.
J. Biol. Chem. 262(24) , 11641-6, (1987) Chloroperoxidase and H2O2 oxidize styrene to styrene oxide and phenylacetaldehyde but not benzaldehyde. The epoxide oxygen is shown by studies with H2(18)O2 to derive quantitatively from the peroxide. The epoxidation of trans-[1-2H]styrene by chloroperoxidase... |
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A facile synthesis of 4-alkoxymethylphenols by a copper (II)-acetoxime catalyst/O2 system. Shimizu M, et al.
Tetrahedron Lett. 32(18) , 2053-2056, (1991)
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How allosteric effectors can bind to the same protein residue and produce opposite shifts in the allosteric equilibrium.
Biochemistry 34(46) , 15006-20, (1995) Monoaldehyde allosteric effectors of hemoglobin were designed, using molecular modeling software (GRID), to form a Schiff base adduct with the Val 1 alpha N-terminal nitrogens and interact via a salt bridge with Arg 141 alpha of the opposite subunit. The desi... |