cas 1049676-92-7|| where to buy 2-tert-Butyl-6-methyl-1h-indole

Product Name:2-tert-Butyl-6-methyl-1h-indole

IUPAC Name:2-tert-butyl-6-methyl-1H-indole

: CAS：1049676-92-7; Molecular Formula：C13H17N; Purity：95%+

: Catalog Number：CM736551; Molecular Weight：187.29

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Product Details

: CAS NO:1049676-92-7; Molecular Formula:C13H17N; Melting Point:-; Smiles Code:CC1=CC2=C(C=C(N2)C(C)(C)C)C=C1; Density:

: Catalog Number:CM736551; Molecular Weight:187.29; Boiling Point:; MDL No:MFCD11052309; Storage:

Category Infos

: Indoles; Indole is a compound of pyrrole and benzene in parallel, also known as benzopyrrole. There are two combinations of pyrrole and benzene, called indole and isoindole, respectively. Many derivatives of indole have physiological and pharmacological activities, and can synthesize vasodilators, antihistamines, antipyretic analgesics, etc. in medicine, so indole is also a very important heterocyclic compound.; indole company; As a indole company,we sincerely welcome the new and old friends from home and abroad to synergize with our company and share the benefits and opportunities.

Product Other Information

Product Overview	2-tert-Butyl-6-methyl-1H-indole (2-TBM-I) is a heterocyclic aromatic compound that is used in a variety of scientific applications.
Synthesis Method	2-tert-butyl-6-Methyl-1H-indole can be synthesized by several methods, including the reaction of 2-bromo-6-methyl-1H-indole with tert-butyl alcohol in the presence of sodium hydride, or the reaction of 2-bromo-6-methyl-1H-indole with tert-butyl chloride in the presence of a base such as sodium hydride or potassium tert-butoxide. Other methods of synthesis include the reaction of 2-bromo-6-methyl-1H-indole with tert-butylmagnesium chloride, or the reaction of 2-bromo-6-methyl-1H-indole with tert-butyl bromide in the presence of a base.
Chemical Properties	It is low cost, its ease of synthesis, and its stability. It is also non-toxic and non-irritating, and it is soluble in a variety of solvents. However, its use in laboratory experiments is limited by its low solubility in water, and its low bioavailability.
Synthesis and Application	2-tert-butyl-6-Methyl-1H-indole is used in a variety of scientific research applications, including the synthesis of biologically active compounds, the study of enzyme-catalyzed reactions, and the study of the effects of drugs on the body. It is also used in the synthesis of drug metabolites, and in the study of drug-receptor interactions. It has been used in the study of the effects of drugs on the central nervous system, and in the study of the mechanisms of drug action.
Future Directions	Future research on 2-tert-butyl-6-Methyl-1H-indole could focus on its mechanism of action, its biochemical and physiological effects, and its potential therapeutic applications. It could also be studied in more detail to determine its efficacy and safety in humans. Additionally, further research could be conducted to determine the optimal synthesis method for 2-tert-butyl-6-Methyl-1H-indole, and to identify potential new uses for the compound.