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5-Methoxy-2-methylindole, 99+%, Thermo Scientific Chemicals

Catalog Number 11459277
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Quantity:
1 g
5 g
25 g
This item is not returnable. View return policy
1076-74-0
C10H11NO
161.20
MFCD00005620
VSWGLJOQFUMFOQ-UHFFFAOYSA-N
5-methoxy-2-methylindole, 2-methyl-5-methoxyindole, 1h-indole, 5-methoxy-2-methyl, indole, 5-methoxy-2-methyl, pubchem7236, acmc-1buiu, maybridge1_002343, 5-methoxy-2 methylindole, 2-methyl-5-methoxylindole, 2-methyl-5-methoxy indole
70642
5-methoxy-2-methyl-1H-indole
COC1=CC=C2NC(C)=CC2=C1
This item is not returnable. View return policy
1076-74-0
C10H11NO
161.20
MFCD00005620
VSWGLJOQFUMFOQ-UHFFFAOYSA-N
5-methoxy-2-methylindole, 2-methyl-5-methoxyindole, 1h-indole, 5-methoxy-2-methyl, indole, 5-methoxy-2-methyl, pubchem7236, acmc-1buiu, maybridge1_002343, 5-methoxy-2 methylindole, 2-methyl-5-methoxylindole, 2-methyl-5-methoxy indole
70642
5-methoxy-2-methyl-1H-indole
COC1=CC=C2NC(C)=CC2=C1

It is employed as a reactant in preparation of indolylquinoxalines by condensation reactions, reactant in preparation of alkylindoles via Ir-catalyzed reductive alkylation, reactant in arylation reactions using a palladium acetate catalyst, reactant in enantioselective Friedel-Crafts alkylation and reactant in stereoselective synthesis of cyclopentaindolones via stereoselective [3+2] cyclopentannulation. As an indole derivative shown to be an effective inhibitor of the chlorinating activity of myeloperoxidase (MPO). Used in the metabolic synthesis of arylacetic acid anti-inflammatory synthesis.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
It is employed as a reactant in preparation of indolylquinoxalines by condensation reactions, reactant in preparation of alkylindoles via Ir-catalyzed reductive alkylation, reactant in arylation reactions using a palladium acetate catalyst, reactant in enantioselective Friedel-Crafts alkylation and reactant in stereoselective synthesis of cyclopentaindolones via stereoselective [3+2] cyclopentannulation. As an indole derivative shown to be an effective inhibitor of the chlorinating activity of myeloperoxidase (MPO). Used in the metabolic synthesis of arylacetic acid anti-inflammatory synthesis.

Solubility
Soluble in methanol (very faint turbidity.)

Notes
Store away from oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.
TRUSTED_SUSTAINABILITY
Melting Point 85°C to 88°C
Quantity 5 g
Sensitivity Light sensitive
Solubility Information Soluble in methanol (very faint turbidity.)
Formula Weight 161.2
Percent Purity ≥99%
Chemical Name or Material 5-Methoxy-2-methylindole

RUO – Research Use Only

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