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Catalog Number:
40093
CAS Number:
1025456-44-3
[2,2'-Binaphthalen]-6-ylboronic acid
Purity:
95 - 105% (Assay by titration)
Documents
$356.03 /1G
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Product Information

[2,2'-Binaphthalen]-6-ylboronic acid is a versatile compound widely recognized for its applications in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the formation of biaryl compounds. Researchers and industry professionals utilize this compound to create complex organic molecules, which are crucial in the development of pharmaceuticals, agrochemicals, and advanced materials. Its unique structure allows for selective functionalization, providing an edge in the synthesis of compounds with specific properties.

In addition to its synthetic utility, [2,2'-Binaphthalen]-6-ylboronic acid exhibits potential in the field of sensor technology and catalysis. Its boron atom can form reversible covalent bonds with various substrates, enhancing its applicability in sensor design for detecting biomolecules. This compound stands out due to its high stability and reactivity, making it a preferred choice for researchers looking to streamline their synthetic processes while achieving high yields. Overall, [2,2'-Binaphthalen]-6-ylboronic acid is a valuable asset for professionals seeking innovative solutions in chemical synthesis and material science.

CAS Number
1025456-44-3
Purity
95 - 105% (Assay by titration)
Molecular Formula
C20H15BO2
Molecular Weight
298.15
MDL Number
MFCD30478552
PubChem ID
59524096
Appearance
White to light yellow crystalline powder
Conditions
Store at RT
General Information
CAS Number
1025456-44-3
Purity
95 - 105% (Assay by titration)
Molecular Formula
C20H15BO2
Molecular Weight
298.15
MDL Number
MFCD30478552
PubChem ID
59524096
Appearance
White to light yellow crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

[2,2'-Binaphthalen]-6-ylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a crucial building block in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Catalysis: It is employed as a ligand in various catalytic processes, enhancing reaction efficiency and selectivity in organic reactions, which is vital for the production of fine chemicals.
  • Material Science: The compound is used in the fabrication of advanced materials, including polymers and nanomaterials, which are essential in electronics and coatings.
  • Bioconjugation: Its boronic acid functionality allows for selective binding to diols, making it useful in bioconjugation techniques for drug delivery systems and biomolecule labeling.
  • Research in Medicinal Chemistry: It plays a significant role in the design of targeted therapies, particularly in cancer research, by facilitating the development of boron-containing compounds that can enhance the efficacy of treatment.

Citations