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627526-50-5

4,4,5,5-Tetramethyl-2-(4-methylnaphthalen-1-yl)-1,3,2-dioxaborolane

Catalog#: AR00ELE8  |   CAS#: 627526-50-5  |   MDL#: MFCD20231463  |   MF: C17H21BO2  |   MW: 268.1584

Packsize Purity Price Availability Quantity
100mg 97% $10.00 Global Stock Buy Now Add To Cart
250mg 97% $15.00 Global Stock Buy Now Add To Cart
1g 97% $31.00 Global Stock Buy Now Add To Cart
5g 97% $133.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00ELE8
Chemical Name 4,4,5,5-Tetramethyl-2-(4-methylnaphthalen-1-yl)-1,3,2-dioxaborolane
CAS Number 627526-50-5
Molecular Formula C17H21BO2
Molecular Weight 268.1584
MDL Number MFCD20231463
SMILES Cc1ccc(c2c1cccc2)B1OC(C(O1)(C)C)(C)C

4,4,5,5-Tetramethyl-2-(4-methylnaphthalen-1-yl)-1,3,2-dioxaborolane, also known as $name$, is a versatile compound commonly utilized in chemical synthesis. Its primary application lies in the field of organic chemistry, where it serves as a key building block for the creation of various functional molecules.One of the key roles of $name$ in chemical synthesis is as a boron-containing reagent. Boron compounds are highly valuable in organic synthesis due to their ability to participate in a wide range of reactions, such as Suzuki-Miyaura cross-coupling, which is a fundamental tool in the construction of carbon-carbon bonds. By incorporating $name$ into a reaction mixture, chemists can efficiently introduce the boron functionality into target molecules, facilitating further transformations and the creation of complex molecular structures.Additionally, the unique structural features of $name$, including the bulky tetramethyl and methylnaphthalenyl groups, offer strategic advantages in controlling the reactivity and selectivity of chemical reactions. These steric influences can direct the course of a synthetic pathway, enabling chemists to access specific molecular architectures with high precision and efficiency.In summary, the application of 4,4,5,5-Tetramethyl-2-(4-methylnaphthalen-1-yl)-1,3,2-dioxaborolane in chemical synthesis encompasses its role as a versatile boron-containing reagent with unique steric properties, enabling the efficient construction of complex organic molecules for various scientific and industrial purposes.
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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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