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Methyl 3-indolecarboxylate

CAS# 942-24-5

Methyl 3-indolecarboxylate

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Methyl 3-indolecarboxylate: 5mg $6 In Stock
Methyl 3-indolecarboxylate: 10mg Please Inquire In Stock
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Quality Control of Methyl 3-indolecarboxylate

Number of papers citing our products

Chemical structure

Methyl 3-indolecarboxylate

3D structure

Chemical Properties of Methyl 3-indolecarboxylate

Cas No. 942-24-5 SDF Download SDF
PubChem ID 589098 Appearance Powder
Formula C10H9NO2 M.Wt 175.2
Type of Compound Alkaloids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name methyl 1H-indole-3-carboxylate
SMILES COC(=O)C1=CNC2=CC=CC=C21
Standard InChIKey QXAUTQFAWKKNLM-UHFFFAOYSA-N
Standard InChI InChI=1S/C10H9NO2/c1-13-10(12)8-6-11-9-5-3-2-4-7(8)9/h2-6,11H,1H3
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Source of Methyl 3-indolecarboxylate

The roots of Heracleum candicans

Biological Activity of Methyl 3-indolecarboxylate

DescriptionMethyl 3-indolecarboxylate is a natural product fom Heracleum candicans.

Protocol of Methyl 3-indolecarboxylate

Structure Identification
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.

Methyl 3-indolecarboxylate Dilution Calculator

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Methyl 3-indolecarboxylate Molarity Calculator

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Preparing Stock Solutions of Methyl 3-indolecarboxylate

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 5.7078 mL 28.5388 mL 57.0776 mL 114.1553 mL 142.6941 mL
5 mM 1.1416 mL 5.7078 mL 11.4155 mL 22.8311 mL 28.5388 mL
10 mM 0.5708 mL 2.8539 mL 5.7078 mL 11.4155 mL 14.2694 mL
50 mM 0.1142 mL 0.5708 mL 1.1416 mL 2.2831 mL 2.8539 mL
100 mM 0.0571 mL 0.2854 mL 0.5708 mL 1.1416 mL 1.4269 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on Methyl 3-indolecarboxylate

Regioselective dibromination of methyl indole-3-carboxylate and application in the synthesis of 5,6-dibromoindoles.[Pubmed:21643565]

Org Biomol Chem. 2011 Jul 21;9(14):5021-3.

Treatment of methyl indole-3-carboxylate 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. 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.

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