487-68-3
Chemical Structure
Mesitaldehyde
Synonym(s): 2,4,6-Trimethylbenzaldehyde
- CAS No.: 487-68-3
- Formula:C10H12O
- Molecular Weight:148.21
IUPAC Name: 2,4,6-trimethylbenzaldehyde
InChIKey: HIKRJHFHGKZKRI-UHFFFAOYSA-N
SMILES: O=CC1=C(C)C=C(C)C=C1C
Biological Activity: Mesitaldehyde (2,4,6-Trimethylbenzaldehyde) is an ortho-alkyl benzaldehyde and a substrate for photocyclization. When excited by light in the solid state, mesitaldehyde undergoes γ-hydrogen abstraction, which generates a triplet-excited 1,4-diradical or enol intermediate and forms benzocyclobutenol. Mesitaldehyde produces benzocyclobutenol as the sole product with high selectivity via photolysis of its solid-state inclusion complex; in contrast, its photolysis in solution yields a mixture of cyclobutenol and trimesic acid[1].
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Mesitaldehyde | 98.13% | Mesitaldehyde (2,4,6-Trimethylbenzaldehyde) is an ortho-alkyl benzaldehyde and a substrate for photocyclization. When excited by light in the solid state, mesitaldehyde undergoes γ-hydrogen abstraction, which generates a triplet-excited 1,4-diradical or enol intermediate and forms benzocyclobutenol. Mesitaldehyde produces benzocyclobutenol as the sole product with high selectivity via photolysis of its solid-state inclusion complex; in contrast, its photolysis in solution yields a mixture of cyclobutenol and trimesic acid. | ||||||||||||||||||||
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Mesitaldehyde (Standard) | ≥98% | Mesitaldehyde is an endogenous metabolite. | ||||||||||||||||||||
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