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5-Methoxy-2-methylindole, 99+%

CAS: 1076-74-0 | C10H11NO | 161.20 g/mol

$73.78 - $868.53

Chemical Identifiers

CAS 1076-74-0
Molecular Formula C10H11NO
Molecular Weight (g/mol) 161.20
MDL Number MFCD00005620
InChI Key VSWGLJOQFUMFOQ-UHFFFAOYSA-N
Synonym 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
PubChem CID 70642
IUPAC Name 5-methoxy-2-methyl-1H-indole
SMILES COC1=CC=C2NC(C)=CC2=C1
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AAB2134803
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Thermo Scientific Chemicals
B2134803
1 g
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AAB2134806
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B2134806
5 g
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AAB2134814
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B2134814
25 g
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Description

Description

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.
Specifications

Chemical Identifiers

1076-74-0
161.20
VSWGLJOQFUMFOQ-UHFFFAOYSA-N
70642
COC1=CC=C2NC(C)=CC2=C1
C10H11NO
MFCD00005620
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
5-methoxy-2-methyl-1H-indole

Specifications

1076-74-0
C10H11NO
1 g
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
VSWGLJOQFUMFOQ-UHFFFAOYSA-N
5-methoxy-2-methyl-1H-indole
70642
≥99%
85°C to 88°C
MFCD00005620
Light sensitive
Soluble in methanol (very faint turbidity.)
COC1=CC=C2NC(C)=CC2=C1
161.20
161.2
5-Methoxy-2-methylindole
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Safety and Handling

Safety and Handling

P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c

H315-H319-H335

EINECSNumber : 214-066-5

TSCA : No

Recommended Storage : Keep cold

SDS
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RUO – Research Use Only