5-METHOXY-2-METHYLINDOLE

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Company Name: Capot Chemical Co.,Ltd.
Tel: 571-85586718 +8613336195806
Email: sales@capotchem.com
Products Intro: Product Name:5-Methoxy-2-methylindole
CAS:1076-74-0
Purity:0.98 Package:100KG;10KG;5KG;1KG
Company Name: Hangzhou FandaChem Co.,Ltd.
Tel: 008657128800458; +8615858145714
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Products Intro: Product Name:5-METHOXY-2-METHYLINDOLE
CAS:1076-74-0
Company Name: Fluoropharm Co., Ltd.
Tel: +8613336034509
Email: sales@fluoropharm.com
Products Intro: Product Name:5-Methoxy-2-methylindole
CAS:1076-74-0
Purity:0.98 Package:25KG;5KG;1KG Remarks:Mature product
Company Name: career henan chemical co
Tel: +86-0371-86658258
Email: sales@coreychem.com
Products Intro: Product Name:5-METHOXY-2-METHYLINDOLE
CAS:1076-74-0
Purity:98% Package:1kg;1USD
Company Name: Zhejiang ZETian Fine Chemicals Co. LTD
Tel: 18957127338
Email: stella@zetchem.com
Products Intro: Product Name:5-METHOXY-2-METHYLINDOLE
CAS:1076-74-0
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5-METHOXY-2-METHYLINDOLE manufacturers

5-METHOXY-2-METHYLINDOLE Basic information
Product Name:5-METHOXY-2-METHYLINDOLE
Synonyms:5-Methoxy-2-methylindole, 99+%;5-METHOXY-2-METHYLINDOLE;AKOS JY2082626;5-Methoxy-2-methyindole;Indole, 5-methoxy-2-methyl-;5-Methoxy-2-Methylindole, 99+% 25GR;5-Methoxy-2-Methylindole, 99+% 5GR;2-Methyl-5-Methoxyindole
CAS:1076-74-0
MF:C10H11NO
MW:161.2
EINECS:214-066-5
Product Categories:Building Blocks;C10;Chemical Synthesis;Heterocyclic Building Blocks;Aromatics;Heterocycles;Inhibitors;Intermediates & Fine Chemicals;Pharmaceuticals;Indoles;Simple Indoles;Building Blocks;Heterocyclic Building Blocks;Indole;Indoles and derivatives
Mol File:1076-74-0.mol
5-METHOXY-2-METHYLINDOLE Structure
5-METHOXY-2-METHYLINDOLE Chemical Properties
Melting point 86-88 °C (lit.)
Boiling point 145 °C / 1.5mmHg
density 1.0840 (rough estimate)
refractive index 1.5200 (estimate)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Soluble in methanol (very faint turbidity.)
pka17.28±0.30(Predicted)
form Crystalline Powder or Crystals
color White to light beige
InChIKeyVSWGLJOQFUMFOQ-UHFFFAOYSA-N
CAS DataBase Reference1076-74-0(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 37/39-26
WGK Germany 3
HazardClass IRRITANT
HS Code 29339900
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
5-METHOXY-2-METHYLINDOLE Usage And Synthesis
Description5-methoxy-2-methylindole is a useful organic raw material. It can be used as the reactant in the preparation of indolylquinoxalines by condensation reactions, in preparation of alkylindoles via Ir-catalyzed reductive alkylation, in arylation reactions in the presence of a palladium acetate catalyst, in enantioselective Friedel-Crafts alkylation, as well as in stereo selective synthesis of cyclopentaindolones via stereoselective [3+2] cyclopentannulation. It is also employed in inhibiting the chlorinating activity of myeloperoxidase (MPO) and in the metabolic synthesis of acrylacetic acid anti-inflammatory synthesis.
Chemical Propertieswhite to light beige crystalline powder or
UsesIt 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.
Usesreactant in preparation of indolylquinoxalines by condensation reactions1reactant in preparation of alkylindoles via Ir-catalyzed reductive alkylation2reactant in arylation reactions using a palladium acetate catalyst3reactant in enantioselective Friedel-Crafts alkylation4reactant in stereoselective synthesis of cyclopentaindolones via stereoselective [3+2] cyclopentannulation5
UsesAn indole derivative shown to be an effective inhibitor of the chlorinating activity of myeloperoxidase (MPO). Used in the metabolic synthesis of arylacetic acid antiinflammatory synthesis.
DefinitionChEBI: 5-Methoxy-2-methyl-1H-indole is a member of indoles.
Referenceshttps://www.alfa.com/en/catalog/B21348/
http://www.sigmaaldrich.com/catalog/product/aldrich/m15451?lang=en&region=US
https://pubchem.ncbi.nlm.nih.gov/compound/5-Methoxy-2-methylindole#section=2D-Structure
Tag:5-METHOXY-2-METHYLINDOLE(1076-74-0) Related Product Information
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