logo
Home  > Chemistry  > Heterocyclic Building Blocks  > Other Aliphatic Heterocycles  > Bis(neopentyl glycolato)diboron

AB03226

201733-56-4 | Bis(neopentyl glycolato)diboron

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.

Description
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

 

Computed Properties
Complexity: 211  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 16  
Hydrogen Bond Acceptor Count: 4  
Rotatable Bond Count: 1  

 

 

Upstream Synthesis Route
  • 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.
FEATURED PRODUCTS