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1201657-84-2

3-Ureidophenylboronic acid pincol ester

Catalog#: AR0094X3  |   CAS#: 1201657-84-2  |   MDL#: MFCD18383950  |   MF: C13H19BN2O3  |   MW: 262.1126

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Catalog Number AR0094X3
Chemical Name 3-Ureidophenylboronic acid pincol ester
CAS Number 1201657-84-2
Molecular Formula C13H19BN2O3
Molecular Weight 262.1126
MDL Number MFCD18383950
SMILES NC(=O)Nc1cccc(c1)B1OC(C(O1)(C)C)(C)C 

N-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]urea is a versatile compound commonly used in chemical synthesis as a key reagent for the preparation of various organic molecules. Specifically, this compound serves as an important building block in the construction of complex structures through the formation of carbon-carbon or carbon-nitrogen bonds.In organic synthesis, N-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]urea is utilized as a source of both the urea functionality and the boronic ester functionality. The boronic ester moiety is crucial for facilitating cross-coupling reactions with various electrophiles such as aryl halides or triflates. This reactivity allows for the selective incorporation of the N-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]urea unit into more complex molecular frameworks.Furthermore, the presence of the tetramethyl dioxaborolane group enhances the stability and reactivity of the compound, making it a valuable tool for chemists working in the field of synthetic organic chemistry. By leveraging the unique properties of N-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]urea, researchers can efficiently access a diverse array of biologically active compounds, materials, and functionalized intermediates for drug discovery, material science, and other chemical applications.
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