For research use only. Not for therapeutic Use.
(2-Aminopyrimidin-5-yl)boronic acid(Cat No.:R072961)is a heteroaromatic boronic acid featuring a pyrimidine ring substituted with an amino group at the 2-position and a boronic acid moiety at the 5-position. It is a valuable intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions for constructing C–C bonds in pharmaceuticals and agrochemicals. This compound enables the functionalization of pyrimidine scaffolds, common in kinase inhibitors and other bioactive molecules. Typically a crystalline solid, it is moisture-sensitive and should be handled under dry conditions with standard protective equipment to ensure stability and safe use.
CAS Number | 936250-22-5 |
Molecular Formula | C4H6BN3O2 |
Purity | ≥95% |
IUPAC Name | (2-aminopyrimidin-5-yl)boronic acid |
InChI | InChI=1S/C4H6BN3O2/c6-4-7-1-3(2-8-4)5(9)10/h1-2,9-10H,(H2,6,7,8) |
InChIKey | CGHYQZASLKERLV-UHFFFAOYSA-N |
SMILES | B(C1=CN=C(N=C1)N)(O)O |
Chemistry Calculators | Dilution Calculator In vivo Formulation Calculator Molarity Calculator Molecular Weight Calculator Reconstitution Calculator |