Methyl 3-indolecarboxylate
Methyl 3-indolecarboxylate is a natural product fom Heracleum candicans.
Inquire / Order:
manager@chemfaces.com
Technical Inquiries:
service@chemfaces.com
Tel:
+86-27-84237783
Fax:
+86-27-84254680
Address:
1 Building, No. 83, CheCheng Rd., Wuhan Economic and Technological Development Zone, Wuhan, Hubei 430056, PRC
Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to
24 months(2-8C).
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.
Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com
The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
Antimicrob Agents Chemother.2024, e0031424.
Exp Parasitol.2018, 194:67-78
Environ Toxicol.2020, doi: 10.1002
Pharmaceuticals (Basel).2024, 17(4):462.
Metab Eng.2022, 75:143-152.
Nutrients.2023, 15(4):954.
Horticulturae2021, 7(1),5.
Br J Pharmacol.2020, 10.1111
Food Chem.2018, 252:207-214
American Association for Anatomy2020, doi: 10.1002.
Related and Featured Products
Org Biomol Chem. 2011 Jul 21;9(14):5021-3.
Regioselective dibromination of methyl indole-3-carboxylate and application in the synthesis of 5,6-dibromoindoles.[Pubmed:
21643565]
METHODS AND RESULTS:
Treatment of methyl indole-3-carboxylate(Methyl 3-indolecarboxylate) with bromine in acetic acid gives methyl 5,6-dibromoindole-3-carboxylate regioselectively, from which the parent 5,6-dibromoindole can be accessed via a one-pot, microwave-mediated ester hydrolysis and decarboxylation.
CONCLUSIONS:
Application of these building blocks in syntheses of natural and non-natural 5,6-dibromoindole derivatives, including meridianin F and 5,6-dibromo-2'-demethylaplysinopsin, is reported.
