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M14951 Aldrich

5-Methoxyindole-2-carboxylic acid

97%

Synonym: NSC 30927

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Properties

Related Categories Building Blocks, C10, Chemical Synthesis, Heterocyclic Building Blocks, Indoles More...
InChI Key   YEBJVSLNUMZXRJ-UHFFFAOYSA-N
assay   97%
mp   199-201 °C(lit.)

Description

Application

Reactant for preparation of:
• Anticancer agents
• A fluorescent small molecule probe for in vivo lipid imaging
• Indoleamine 2,3-dioxygenase (IDO) inhibitors
• Selective Dopamine D3 receptor ligands
• 5-HT4 receptor ligands
• Inhibitors of Mycobacterium tuberculosis pantothenate synthetase
• Hypoxia selective cytotoxins
• Potent antitumor bifunctional DNA alkylating agents

Packaging

5, 10 g in glass bottle

Price and Availability

Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3
RTECS 
NL6005000
Protocols & Articles

Articles

Indoles

Sigma-Aldrich is proud to offer a new series of ChemFiles—called Privileged Structures, to our Drug Discovery and Organic Synthesis customers. Each piece will highlight a specific motif, selected app...
Chemfiles Volume 4 Article 8
Keywords: Applications, Building blocks, Cardiovascular, Chemfiles, Company, Diabetes, Diseases, Drug discovery, Medicinal chemistry, Organic synthesis, Respiratory

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