2,2'-Bi-1,3,2-benzodioxaborole


Chemical Name: 2,2'-Bi-1,3,2-benzodioxaborole
CAS Number: 13826-27-2
Product Number: AG0018F8(AGN-PC-0KV907)
Synonyms:
MDL No:
Molecular Formula: C12H8B2O4
Molecular Weight: 237.8115

Identification/Properties


Computed Properties
Molecular Weight:
237.812g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
238.061g/mol
Monoisotopic Mass:
238.061g/mol
Topological Polar Surface Area:
36.9A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
259
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



2,2'-Bi-1,3,2-benzodioxaborole, also known as $name$, is a versatile compound widely used in chemical synthesis due to its unique reactivity and structural properties. In organic chemistry, $name$ serves as a valuable building block for the construction of various organic molecules. Its boron-containing structure enables it to participate in diverse reactions, making it a valuable tool for creating new chemical entities.One of the key applications of 2,2'-Bi-1,3,2-benzodioxaborole in chemical synthesis is its role as a boron source in Suzuki-Miyaura cross-coupling reactions. This powerful synthetic method allows for the selective formation of carbon-carbon bonds, facilitating the synthesis of complex organic compounds. By incorporating $name$ into the reaction, chemists can introduce functional groups with precision, expanding the scope of accessible chemical structures.Moreover, 2,2'-Bi-1,3,2-benzodioxaborole is also utilized in the synthesis of pharmaceuticals and agrochemicals. Its compatibility with a wide range of functional groups makes it a valuable intermediate in the production of biologically active compounds. Through strategic manipulation of its chemical reactivity, researchers can access novel scaffolds and molecular architectures for drug discovery and development.In summary, 2,2'-Bi-1,3,2-benzodioxaborole plays a crucial role in modern synthetic chemistry as a versatile reagent for creating complex organic molecules. Its utility in Suzuki-Miyaura cross-coupling reactions and its significance in pharmaceutical synthesis highlight its importance in advancing the field of organic chemistry.