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Sku CI21948_5_G
Chem Impex
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Product Information

Product Name
4-Methoxyindole
Brand Name
Chem Impex
Product Number
21948
CAS
4837-90-5
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
138363
IUPAC Name
4-methoxy-1H-indole
InChI Key
LUNOXNMCFPFPMO-UHFFFAOYSA-N
SMILES
COC1=CC=CC2=C1C=CN2

Application

4-Methoxyindole is widely utilized in research focused on:

Pharmaceutical Development: This compound serves as a building block in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting neurological disorders due to its potential neuroprotective properties.

Biological Research: It is used in studies investigating the effects of indole derivatives on cellular processes, helping researchers understand mechanisms of action in cancer and other diseases.

Natural Product Synthesis: 4-Methoxyindole is employed in the synthesis of natural products, enhancing the production of compounds with medicinal properties found in plants.

Material Science: This compound is explored in the development of organic electronic materials, contributing to advancements in flexible electronics and sensors.

Flavor and Fragrance Industry: It finds applications in the formulation of flavors and fragrances, adding unique aromatic qualities to products while being a safer alternative to some synthetic compounds.

References

Structure, mechanism and crystallographic fragment screening of the SARS-CoV-2 NSP13 helicase

Publication Name: Nature Communications
Publication Date: 2021-08-11
DOI: 10.1038/s41467-021-25166-6

Synthesis from 1H-Indoles and 2-Bromo-2′-iodo-1,1′-biphenyl

Publication Name: Science of Synthesis
Publication Date: 2021

Exploration of Iron- and α-Ketoglutarate-Dependent Dioxygenases as Practical Biocatalysts in Natural Product Synthesis

Publication Name: Synlett : accounts and rapid communications in synthetic organic chemistry
Publication Date: 2020-10-26
DOI: 10.1055/s-0040-1707320

Natural control of plant pathogens through glucosinolates: an effective strategy against fungi and oomycetes

Publication Name: Phytochemistry Reviews
Publication Date: 2020-06-16
DOI: 10.1007/s11101-020-09699-0

Reactions of Substituted Indoles with 2,3-Dichloro-1,4-naphthoquinone and Electrochemical Properties of Some 2,3-Substituted 1,4-Naphthoquinones

Publication Name: Russian Journal of Organic Chemistry
Publication Date: 2019-04
DOI: 10.1134/s1070428019040213