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- Indole - Wikipedia
In the 1930s, interest in indole intensified when it became known that the indole substituent is present in many important alkaloids, known as indole alkaloids (e g , tryptophan and auxins), and it remains an active area of research today
- Indole | C8H7N | CID 798 - PubChem
Indole | C8H7N | CID 798 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety hazards toxicity information, supplier lists, and more
- Indole | Aromatic, Biosynthesis, Metabolism | Britannica
Indole, first isolated in 1866, has the molecular formula C 8 H 7 N, and it is commonly synthesized from phenylhydrazine and pyruvic acid, although several other procedures have been discovered
- Indole: Chemical Properties, Synthesis, Applications, and Analysis
Learn about indole, its chemical properties, synthesis methods, biological role, applications in industry, and key analysis techniques used in research and industry
- What Are Indoles, and Why Are They Important for Health?
Key Takeaways Indoles have antioxidant, anti-inflammatory, and detoxification-supporting effects Including indole-rich foods in the diet, such as cruciferous vegetables, leafy greens, fruits, and legumes, can help optimize intake of this compound
- Indoles - Chemistry Online
Indole is a weak acid (with a value of pKa = 16 97), with an acidity comparable to pyrrole, and to aliphatic alcohols It can be converted to the N -sodium derivative, in liquid ammonia, or with sodium hydride (NaH) in an organic solvent
- Indole - an overview | ScienceDirect Topics
Presence of an indole nucleus in amino acid tryptophan makes it prominent in phytoconstituents such as perfumes, neurotransmitters, auxins (plant hormones), indole alkaloids, and so on The interesting molecular architecture of indoles makes them suitable candidates for drug development
- Synthesis, Reactions and Medicinal Uses of Indole
Fischer – indole synthesis - Indoles can be made by adding two or three substitutes to this molecule An arylhydrazine is heated with an aldehyde or ketone, then the resulting arylhydrazone is rearranged with acid to give an indole with a loss of ammonia
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