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Catalog Number:
40235
CAS Number:
881302-73-4
3,5-Dicarboxyphenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
3,5-Dicarboxybenzeneboronic acid
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Product Information

3,5-Dicarboxyphenylboronic acid is a versatile compound recognized for its unique boronic acid functionality, making it invaluable in various chemical applications. This compound serves as a crucial building block in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its ability to form reversible covalent bonds with diols enhances its utility in the synthesis of complex molecules, including glycosylated compounds, which are essential in medicinal chemistry and biochemistry. Additionally, 3,5-Dicarboxyphenylboronic acid is employed in the preparation of polymeric materials and as a reagent in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is widely used in the formation of carbon-carbon bonds.

Researchers and industry professionals appreciate this compound for its high reactivity and selectivity, which can lead to more efficient synthetic pathways and reduced by-products compared to similar boronic acids. Its applications extend to sensor technology, where it can be utilized in the detection of sugars and other biomolecules, showcasing its potential in both analytical and diagnostic fields. With its diverse applications and significant advantages in synthetic chemistry, 3,5-Dicarboxyphenylboronic acid is an essential compound for advancing research and development in various industries.

Synonyms
3,5-Dicarboxybenzeneboronic acid
CAS Number
881302-73-4
Purity
97 - 105% (Assay by titration)
Molecular Formula
C8H7BO6
Molecular Weight
209.95
MDL Number
MFCD06203347
PubChem ID
44118570
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
3,5-Dicarboxybenzeneboronic acid
CAS Number
881302-73-4
Purity
97 - 105% (Assay by titration)
Molecular Formula
C8H7BO6
Molecular Weight
209.95
MDL Number
MFCD06203347
PubChem ID
44118570
Appearance
White to off-white 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

3,5-Dicarboxyphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Drug Development: Its ability to form stable complexes with biomolecules makes it valuable in drug design, especially in targeting specific proteins or enzymes in disease pathways.
  • Materials Science: It is used in the creation of advanced materials, including polymers and nanomaterials, which have applications in electronics and coatings.
  • Analytical Chemistry: The compound acts as a reagent in various analytical techniques, aiding in the detection and quantification of certain biomolecules, enhancing the accuracy of research results.
  • Bioconjugation: Its boronic acid functionality allows for selective binding to diols, making it useful in bioconjugation processes for developing targeted drug delivery systems.

Citations