cas 7511-14-0|| where to buy N,N-dimethyl-1H-indole-2-carboxamide

Product Name:N,N-dimethyl-1H-indole-2-carboxamide

IUPAC Name:N,N-dimethyl-1H-indole-2-carboxamide

: CAS：7511-14-0; Molecular Formula：C11H12N2O; Purity：95%+

: Catalog Number：CM240265; Molecular Weight：188.23

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Product Details

: CAS NO:7511-14-0; Molecular Formula:C11H12N2O; Melting Point:-; Smiles Code:O=C(C(N1)=CC2=C1C=CC=C2)N(C)C; Density:

: Catalog Number:CM240265; Molecular Weight:188.23; Boiling Point:; MDL No:; 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.

Column Infos

: Indoles

Product Other Information

Product Overview	N,N-dimethyl-1H-indole-2-carboxamide, also known as DMIC, is a chemical compound that has gained significant attention in scientific research due to its potential applications in various fields. DMIC is a derivative of indole, a heterocyclic organic compound that is widely used in the pharmaceutical industry.
Synthesis and Application	The synthesis of N,N-dimethyl-1H-indole-2-carboxamide involves a multi-step process that starts with the reaction between indole and N,N-dimethylformamide dimethyl acetal (DMF-DMA). This reaction produces an intermediate compound, which is then treated with acetic anhydride and triethylamine to form N,N-dimethyl-1H-indole-2-carboxamide. The final product is obtained through purification using column chromatography. This synthesis method has been optimized to yield high purity N,N-dimethyl-1H-indole-2-carboxamide with good yields. N,N-dimethyl-1H-indole-2-carboxamide has been extensively studied for its potential applications in various scientific fields. One of the most promising applications of N,N-dimethyl-1H-indole-2-carboxamide is in the field of organic electronics. N,N-dimethyl-1H-indole-2-carboxamide has been shown to exhibit excellent electron-transporting properties, making it a potential candidate for use in organic field-effect transistors (OFETs). N,N-dimethyl-1H-indole-2-carboxamide has also been studied for its potential use in organic solar cells, where it has been shown to improve the efficiency of the cells.
Future Directions	There are several future directions for research on N,N-dimethyl-1H-indole-2-carboxamide. One area of research is the development of new synthesis methods for N,N-dimethyl-1H-indole-2-carboxamide that are more efficient and environmentally friendly. Another area of research is the exploration of N,N-dimethyl-1H-indole-2-carboxamide's potential use in organic electronics, including OFETs and organic solar cells. Additionally, further research is needed to fully understand the mechanism of action of N,N-dimethyl-1H-indole-2-carboxamide and its potential applications in the treatment of various diseases.