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1883598-68-2

tert-butyl 5-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate

Catalog#: AR01FOBB  |   CAS#: 1883598-68-2  |   MDL#: MFCD14155741  |   MF: C20H28BNO4  |   MW: 357.2516

Packsize Purity Price Availability Quantity
100mg 98% $135.00 Global Stock Buy Now Add To Cart
250mg 98% $173.00 Global Stock Buy Now Add To Cart
1g 98% $358.00 Global Stock Buy Now Add To Cart
5g 98% $1,071.00 Global Stock Buy Now Add To Cart
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Catalog Number AR01FOBB
Chemical Name tert-butyl 5-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate
CAS Number 1883598-68-2
Molecular Formula C20H28BNO4
Molecular Weight 357.2516
MDL Number MFCD14155741
SMILES Cc1ccc2c(c1)c(cn2C(=O)OC(C)(C)C)B1OC(C(O1)(C)C)(C)C

Through its unique structure, tert-butyl 5-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate serves as a versatile building block in chemical synthesis. This compound plays a crucial role as a key intermediate in the production of various pharmaceuticals, agrochemicals, and advanced materials. Its functionality allows for the introduction of the indole moiety, which is significant in medicinal chemistry due to its diverse biological activities.In synthetic processes, tert-butyl 5-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate can undergo various transformations such as cross-coupling reactions, palladium-catalyzed coupling, and Suzuki-Miyaura reactions. These reactions enable the incorporation of different functional groups or structural modifications, making it a valuable tool for creating complex molecules with tailored properties.Furthermore, this compound's stability and compatibility with a wide range of reaction conditions make it an ideal choice for the synthesis of novel compounds with enhanced biological or physical characteristics. Its application extends to the development of new drug candidates, agricultural chemicals, and materials with specific electronic or optical properties, highlighting its importance in the realm of chemical synthesis.
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