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554453-76-8

(1,2-Dimethyl-1H-imidazol-5-yl)boronic acid

Catalog#: AR0037YY  |   CAS#: 554453-76-8  |   MDL#: MFCD10697444  |   MF: C5H9BN2O2  |   MW: 139.9482

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Catalog Number AR0037YY
Chemical Name (1,2-Dimethyl-1H-imidazol-5-yl)boronic acid
CAS Number 554453-76-8
Molecular Formula C5H9BN2O2
Molecular Weight 139.9482
MDL Number MFCD10697444
SMILES OB(c1cnc(n1C)C)O

(1,2-Dimethyl-1H-imidazol-5-yl)boronic acid, also known as $name$, is a versatile organic compound commonly utilized in chemical synthesis. This boronic acid derivative is particularly valued for its ability to act as a key building block in the creation of complex organic molecules.One significant application of $(1,2-Dimethyl-1H-imidazol-5-yl)boronic acid is in the field of cross-coupling reactions. By employing this compound as a boron source in traditional Suzuki-Miyaura coupling reactions, organic chemists can efficiently and selectively form carbon-carbon bonds between aryl or vinyl halides and various boronic acid derivatives. This enables the synthesis of structurally diverse compounds with high efficiency and precision.Moreover, $(1,2-Dimethyl-1H-imidazol-5-yl)boronic acid can also be utilized in the preparation of pharmaceutical intermediates, agrochemicals, and materials science applications. Its compatibility with a wide range of functional groups and its stability under various reaction conditions make it a valuable tool for synthetic chemists seeking to construct complex molecules in an efficient and controlled manner.Overall, the unique properties and versatile applications of $(1,2-Dimethyl-1H-imidazol-5-yl)boronic acid make it an indispensable reagent in modern organic synthesis, facilitating the development of novel compounds with diverse functionalities and potential industrial applications.
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GHS Pictogram
Signal Word Warning
UN# -
Hazard Statements H302-H315-H319-H335
Precautionary Statements P261-P305+P351+P338
Class -
Packing Group -

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