Molecular structure of 3,4,5-Trimethoxybenzaldehyde, CAS Number: 86-81-7
3,4,5-Trimethoxybenzaldehyde (CAS 86-81-7)
CAS Number:
86-81-7
Purity:
≥99%
Molecular Weight:
196.20
Molecular Formula:
C10H12O4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
QUICK LINKS
Ordering Information
Description
Technical Information
Safety Information
SDS & Certificate of Analysis
3,4,5-Trimethoxybenzaldehyde, a naturally occurring aromatic aldehyde found in various plants and fungi, possesses diverse applications in scientific research. It has been utilized to study enzyme reactions due to its inhibitory effects on specific enzymes. Notably, it acts as an inhibitor for cytochrome P450 enzymes, in metabolizing drugs and other compounds. By binding to these enzymes, it disrupts their proper functioning, leading to metabolic inhibition. Moreover, 3,4,5-Trimethoxybenzaldehyde demonstrates antioxidant properties by scavenging free radicals, thereby safeguarding cells from potential damage.
3,4,5-Trimethoxybenzaldehyde (CAS 86-81-7) References
- Gold-catalyzed post-Ugi alkyne hydroarylation for the synthesis of 2-quinolones. | Du, X., et al. 2018. Beilstein J Org Chem. 14: 2572-2579. PMID: 30410618
- Efficient method for propargylation of aldehydes promoted by allenylboron compounds under microwave irradiation. | Freitas, JJR., et al. 2020. Beilstein J Org Chem. 16: 168-174. PMID: 32117473
- Novel pyrrolizines bearing 3,4,5-trimethoxyphenyl moiety: design, synthesis, molecular docking, and biological evaluation as potential multi-target cytotoxic agents. | Shawky, AM., et al. 2021. J Enzyme Inhib Med Chem. 36: 1313-1333. PMID: 34154478
- Attempts to Access a Series of Pyrazoles Lead to New Hydrazones with Antifungal Potential against Candida species including Azole-Resistant Strains. | Negru, G., et al. 2021. Molecules. 26: PMID: 34641405
- Recent strategies and tactics for the enantioselective total syntheses of cyclolignan natural products. | Reynolds, RG., et al. 2022. Nat Prod Rep. 39: 670-702. PMID: 34664594
- Validated Quantitative 1H NMR Method for Simultaneous Quantification of Indole Alkaloids in Uncaria rhynchophylla. | Yin, T., et al. 2021. ACS Omega. 6: 31810-31817. PMID: 34870003
- Near-infrared light photocatalysis enabled by a ruthenium complex-integrated metal-organic framework via two-photon absorption. | Tang, JH., et al. 2022. iScience. 25: 104064. PMID: 35355522
- On the Nature of Guest Complexation in Water: Triggered Wetting-Water-Mediated Binding. | Suating, P., et al. 2022. J Phys Chem B. 126: 3150-3160. PMID: 35438501
- An Organic Chemist's Guide to Mediated Laccase Oxidation. | Obleser, K., et al. 2022. Chembiochem. 23: e202200411. PMID: 36148536
- Nickel-Catalyzed Enantioselective Coupling of Aldehydes and Electron-Deficient 1,3-Dienes Following an Inverse Regiochemical Course. | Davies, TQ., et al. 2022. J Am Chem Soc. 144: 18817-18822. PMID: 36194199
- Continuous-Flow Divergent Lithiation of 2,3-Dihalopyridines: Deprotolithiation versus Halogen Dance. | Brégent, T., et al. 2022. Chemistry. 28: e202202286. PMID: 36200571
- Chemically Recyclable Dithioacetal Polymers via Reversible Entropy-Driven Ring-Opening Polymerization. | Kariyawasam, LS., et al. 2023. Angew Chem Int Ed Engl. 62: e202303039. PMID: 36988027
- Headspace with Gas Chromatography-Mass Spectrometry for the Use of Volatile Organic Compound Profile in Botanical Origin Authentication of Honey. | Castell, A., et al. 2023. Molecules. 28: PMID: 37298771
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
3,4,5-Trimethoxybenzaldehyde, 25 g | sc-238666 | 25 g | $20.00 |