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Catalog Number:
39971
CAS Number:
269410-07-3
1,2-Benzenediboronic acid bis(pinacol) ester
Purity:
≥ 98% (GC)
Synonym(s):
1,2-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene, 1,2-Phenylenebis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane)
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Product Information

1,2-Benzenediboronic acid bis(pinacol) ester is a versatile compound widely utilized in organic synthesis and materials science. This compound serves as a crucial building block in the development of various organic materials, particularly in the synthesis of polymers and advanced materials. Its unique structure allows for effective cross-coupling reactions, making it an essential reagent in the formation of carbon-carbon bonds. Researchers and industry professionals leverage its properties to create complex molecular architectures, which are pivotal in fields such as drug discovery and the development of organic electronic devices.

Additionally, 1,2-Benzenediboronic acid bis(pinacol) ester exhibits excellent stability and solubility in organic solvents, enhancing its applicability in various chemical reactions. Its ability to participate in Suzuki-Miyaura coupling reactions further underscores its significance in the synthesis of biaryl compounds, which are important in pharmaceuticals and agrochemicals. With its robust performance and reliability, this compound stands out as a preferred choice for researchers aiming to innovate in synthetic chemistry and material development.

Synonyms
1,2-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene, 1,2-Phenylenebis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane)
CAS Number
269410-07-3
Purity
≥ 98% (GC)
Molecular Formula
C18H28B2O4
Molecular Weight
330.04
MDL Number
MFCD28969469
PubChem ID
21923918
Melting Point
116 ?C (Lit.)
Appearance
White to orange crystalline powder
Conditions
Store at RT
General Information
Synonyms
1,2-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene, 1,2-Phenylenebis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane)
CAS Number
269410-07-3
Purity
≥ 98% (GC)
Molecular Formula
C18H28B2O4
Molecular Weight
330.04
MDL Number
MFCD28969469
PubChem ID
21923918
Melting Point
116 ?C (Lit.)
Appearance
White to orange 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

1,2-Benzenediboronic acid bis(pinacol) ester is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key intermediate in the synthesis of complex organic molecules, enabling researchers to create new pharmaceuticals and agrochemicals efficiently.
  • Cross-Coupling Reactions: It is commonly used in Suzuki-Miyaura coupling reactions, which are essential for forming carbon-carbon bonds in the development of various organic compounds, particularly in the field of medicinal chemistry.
  • Material Science: The compound is applied in the production of advanced materials, such as polymers and nanomaterials, which have applications in electronics and coatings, enhancing their performance and durability.
  • Bioconjugation: Its unique boronic acid functionality allows for selective binding to diols, making it useful in bioconjugation techniques for labeling biomolecules, which is crucial in drug delivery and diagnostic applications.
  • Fluorescent Probes: This chemical can be utilized in the development of fluorescent probes for biological imaging, providing researchers with tools to visualize cellular processes in real-time.

Citations