It serves as a boronic ester building block in Suzuki–Miyaura cross-coupling reactions to form complex biaryl compounds. It often serves in medicinal chemistry for developing drug candidates (e.g., kinase inhibitors and other heterocyclic drugs). N-2-pyridinyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide is mainly used as a pharmaceutical and organic synthesis intermediate.
N-2-pyridinyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
| API Name | Acalabrutinib |
|---|---|
| CAS No | 1383385-64-5 |
| Molecular Formula | C18H21BN2O3 |
| Molecular Weight | 324.2 g/mol |
| Synonyms | N-pyridin-2-yl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide |
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Frequently Asked Questions
It serves as a boronic ester building block in Suzuki–Miyaura cross-coupling reactions to form complex biaryl compounds. It often serves in medicinal chemistry for developing drug candidates (e.g., kinase inhibitors and other heterocyclic drugs). N-2-pyridinyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide is mainly used as a pharmaceutical and organic synthesis intermediate.
The CAS number of N-2-pyridinyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide is 1383385-64-5.
The molecular formula of N-2-pyridinyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide is C18H21BN2O3.
The listed molecular weight of N-2-pyridinyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide is 324.2 g/mol.
N-2-pyridinyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide is listed as being used in connection with the following API: Acalabrutinib.
The listed synonym or IUPAC name for N-2-pyridinyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide is N-pyridin-2-yl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide.