CAS 4335-12-0
:5,7-dimethoxy-6-(3-methylbut-2-en-1-yl)-2H-chromen-2-one
Description:
5,7-Dimethoxy-6-(3-methylbut-2-en-1-yl)-2H-chromen-2-one, with the CAS number 4335-12-0, is a chemical compound belonging to the class of flavonoids, specifically a type of chromone. This compound features a chromone backbone, characterized by a benzopyran structure, which is substituted at the 5 and 7 positions with methoxy groups, enhancing its solubility and potential biological activity. The presence of the 3-methylbut-2-en-1-yl group at the 6 position introduces additional hydrophobic characteristics, which may influence its interaction with biological systems. Flavonoids are known for their antioxidant properties, and this compound may exhibit similar activities, potentially contributing to various health benefits. Its structural features suggest potential applications in pharmaceuticals, particularly in the development of natural products with therapeutic properties. However, specific biological activities, toxicity, and pharmacokinetics would require further investigation to fully understand its potential uses and effects.
Formula:C16H18O4
InChI:InChI=1/C16H18O4/c1-10(2)5-6-11-13(18-3)9-14-12(16(11)19-4)7-8-15(17)20-14/h5,7-9H,6H2,1-4H3
InChI key:InChIKey=KRQHZFHWEAJPNO-UHFFFAOYSA-N
SMILES:O(C)C1=C2C(=CC(OC)=C1CC=C(C)C)OC(=O)C=C2
Synonyms:- 2H-1-Benzopyran-2-one, 5,7-dimethoxy-6-(3-methyl-2-buten-1-yl)-
- 2H-1-Benzopyran-2-one, 5,7-dimethoxy-6-(3-methyl-2-butenyl)-
- 5,7-Dimethoxy-6-(3-methyl-2-buten-1-yl)-2H-1-benzopyran-2-one
- Coumarin, 5,7-dimethoxy-6-(3-methyl-2-butenyl)-
- Toddaculin
- Toddaculine
- 6-(3-Methyl-2-butenyl)-5,7-dimethoxy-2H-1-benzopyran-2-one
- 5,7-dimethoxy-6-(3'-methyl-2'-butenyl)coumarin
- 5,7-Dimethoxy-6-(3-methyl-2-butenyl)-2H-1-benzopyran-2-one
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Found 6 products.
6-(3-Methyl-2-butenyl)-5,7-dimethoxy-2H-1-benzopyran-2-one
CAS:Formula:C16H18O4Purity:95%Molecular weight:274.3117Toddaculin
CAS:<p>Toddaculine may be beneficial for the prevention and treatment of osteoporosis, it can not only inhibit the differentiation of osteoclasts via activation of the</p>Formula:C16H18O4Purity:99.91%Color and Shape:SolidMolecular weight:274.31Toddaculin
CAS:<p>Toddaculin is a synthetic peptide derivative, which is produced through a complex process of peptide synthesis techniques involving solid-phase peptide synthesis (SPPS) and advanced chromatography for purification. Its mode of action involves specific binding to neuronal receptors, modulating synaptic activity and influencing neurotransmitter release. This allows for precise studies of synaptic mechanisms and neural network behavior.<br><br>In the realm of neuroscience research, Toddaculin is applied to investigate synaptic plasticity, neuroregulation, and signal transduction pathways. Its precise interactions with neuronal receptors make it a valuable tool for studying the pharmacodynamics of neurological processes and potential therapeutic targets for neurodegenerative diseases. Toddaculin's unique properties facilitate the exploration of cellular responses and neural pathway modulations under controlled experimental conditions.</p>Formula:C16H18O4Purity:Min. 95%Molecular weight:274.31 g/mol






