1218791-47-9

Basic information

• Product Name: N-Propyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidin-2-amine
• Synonyms: 2-Propylaminopyrimidine-5-boronic acid, pinacol ester;N-Propyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidin-2-amine
• CAS NO: 1218791-47-9
• Molecular Formula: C13H22BN3O2
• Molecular Weight: 263.14368
• Mol File: 1218791-47-9.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 396.1±34.0 °C(Predicted)
• Appearance: /
• Density: 1.06±0.1 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 3.80±0.10(Predicted)
• CAS DataBase Reference: N-Propyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidin-2-amine(CAS DataBase Reference)
• NIST Chemistry Reference: N-Propyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidin-2-amine(1218791-47-9)
• EPA Substance Registry System: N-Propyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidin-2-amine(1218791-47-9)

Safety Data

• Hazardous Substances Data: 1218791-47-9(Hazardous Substances Data)

Usage

General Description

N-Propyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidin-2-amine is a chemical compound that contains a pyrimidine ring structure with a propyl group and a boronate ester functional group attached. It is often used as a building block in the synthesis of various organic compounds and pharmaceuticals. The boronate ester moiety is known for its ability to form reversible covalent bonds with certain biomolecules, making this compound potentially useful in the development of targeted drug delivery systems. Additionally, the presence of a propyl group in its molecular structure can influence its solubility and reactivity in certain chemical reactions. Overall, N-Propyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidin-2-amine has potential applications in medicinal chemistry and bioconjugation chemistry due to its unique chemical properties.