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Sku CI21873_1_G
Chem Impex
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Product Information

Product Name
6-Methoxyindole
Brand Name
Chem Impex
Product Number
21873
CAS
3189-13-7
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
76659
IUPAC Name
6-methoxy-1H-indole
InChI Key
QJRWYBIKLXNYLF-UHFFFAOYSA-N
SMILES
COC1=CC2=C(C=C1)C=CN2

Application

6-Methoxyindole is widely utilized in research focused on:

Pharmaceutical Development: This compound serves as a building block in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders due to its ability to interact with serotonin receptors.

Biochemical Research: It is used in studies investigating the role of indole derivatives in cellular signaling pathways, helping researchers understand complex biological processes.

Natural Product Synthesis: 6-Methoxyindole is valuable in the synthesis of natural products, allowing chemists to create compounds with potential therapeutic effects found in nature.

Fluorescent Probes: This chemical can be modified to develop fluorescent probes for imaging applications in biological research, enhancing visualization techniques in cell biology.

Material Science: It finds applications in the development of organic light-emitting diodes (OLEDs), contributing to advancements in display technologies with improved efficiency and color quality.

References

Multimodal action of KRP203 on phosphoinositide kinases in vitro and in cells

Publication Name: Biochemical and Biophysical Research Communications
Publication Date: 2023-10-30
DOI: 10.1016/j.bbrc.2023.08.050

Identification of 7-hydroxyindole as an alternative substrate of MauG by in silico and in vitro analysis

Publication Name: Applied Biological Chemistry
Publication Date: 2023-05-03
DOI: 10.1186/s13765-023-00781-7

A quantitative high-throughput screen identifies compounds that lower expression of the SCA2-and ALS-associated gene ATXN2

Publication Name: The Journal of biological chemistry
Publication Date: 2022-08
DOI: 10.1016/j.jbc.2022.102228

UV-induced –OCH3 rotamerization in a matrix-isolated methoxy-substituted ortho-hydroxyaryl Schiff base

Publication Name: Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology
Publication Date: 2022-01-25
DOI: 10.1007/s43630-021-00166-z

Enzymgesteuerte Indigoproduktion

Publication Name: BIOspektrum
Publication Date: 2018-06-25
DOI: 10.1007/s12268-018-0938-1