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685103-98-4

4-Isoquinolineboronic acid pinacol ester

Catalog#: AR00FB6B  |   CAS#: 685103-98-4  |   MDL#: MFCD05663891  |   MF: C15H18BNO2  |   MW: 255.1199

Packsize Purity Price Availability Quantity
100mg 97% $10.00 Global Stock Buy Now Add To Cart
250mg 97% $14.00 Global Stock Buy Now Add To Cart
1g 97% $37.00 Global Stock Buy Now Add To Cart
5g 97% $126.00 Global Stock Buy Now Add To Cart
10g 97% $217.00 Global Stock Buy Now Add To Cart
25g 97% $433.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00FB6B
Chemical Name 4-Isoquinolineboronic acid pinacol ester
CAS Number 685103-98-4
Molecular Formula C15H18BNO2
Molecular Weight 255.1199
MDL Number MFCD05663891
SMILES CC1(C)OB(OC1(C)C)c1cncc2c1cccc2

4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)isoquinoline is a versatile compound that finds extensive use in chemical synthesis processes. This specific molecule serves as a valuable building block in organic synthesis due to its unique structure and reactivity. By possessing a boron-containing moiety, it provides a platform for diverse functionalization strategies.In chemical synthesis, 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)isoquinoline is commonly employed as a key intermediate for the construction of complex organic molecules. Its boron functionality enables selective cross-coupling reactions with various electrophiles, including aryl halides and pseudohalides. This allows for the formation of new carbon-carbon bonds in a controlled and efficient manner.Furthermore, the presence of the isoquinoline scaffold in this compound imparts additional reactivity and diversity to the synthesis process. The isoquinoline moiety can participate in a range of transformations, such as aromatic substitution reactions and cyclization reactions, leading to structurally intricate and biologically relevant compounds.Overall, the application of 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)isoquinoline in chemical synthesis offers a valuable tool for the construction of complex organic molecules with precise control over regioselectivity and functional group compatibility. This compound's versatile reactivity and structural features make it a valuable asset in the toolkit of synthetic chemists striving to access novel compounds for various applications.
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