AB03226
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
1g | 98% | in stock | $6.00 | $4.00 | - + | |
5g | 98% | in stock | $7.00 | $5.00 | - + | |
10g | 98% | in stock | $9.00 | $6.00 | - + | |
25g | 98% | in stock | $11.00 | $8.00 | - + | |
100g | 98% | in stock | $26.00 | $18.00 | - + | |
500g | 98% | in stock | $125.00 | $87.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AB03226 |
Chemical Name: | Bis(neopentyl glycolato)diboron |
CAS Number: | 201733-56-4 |
Molecular Formula: | C10H20B2O4 |
Molecular Weight: | 225.8854 |
MDL Number: | MFCD02093062 |
SMILES: | CC1(C)COB(OC1)B1OCC(CO1)(C)C |
Complexity: | 211 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 16 |
Hydrogen Bond Acceptor Count: | 4 |
Rotatable Bond Count: | 1 |
5,5,5',5'-Tetramethyl-2,2'-bi(1,3,2-dioxaborinane), commonly referred to as $name$, is a versatile compound frequently utilized in chemical synthesis processes. Due to its unique structure and reactivity, $name$ serves as a valuable building block in the formation of various organic molecules. In particular, it is commonly employed as a boron-containing reagent in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid derivative to facilitate the coupling of aryl or vinyl halides with organic electrophiles. This reaction, catalyzed by palladium, enables the efficient creation of biaryl or polyaryl structures, making $name$ a crucial tool in the construction of complex organic frameworks. Additionally, $name$ can be further functionalized to introduce specific substituents or motifs, expanding its synthetic utility in organic chemistry research and drug discovery applications.