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Catalog Number:
40367
CAS Number:
164014-95-3
1,4-Benzodioxane-6-boronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
3,4-(Ethylenedioxy)benzeneboronic acid
Documents
$178.97 /1G
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Product Information

1,4-Benzodioxane-6-boronic acid is a versatile compound that plays a crucial role in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to form stable complexes with diols, making it invaluable in the development of various pharmaceuticals and agrochemicals. Its unique structure allows for selective reactions, which can enhance the efficiency of synthetic pathways. Researchers often utilize this compound in cross-coupling reactions, particularly in the synthesis of complex organic molecules, including biologically active compounds.

In addition to its synthetic applications, 1,4-Benzodioxane-6-boronic acid is also explored for its potential in drug development, particularly in targeting specific biological pathways. Its compatibility with various functional groups makes it a preferred choice for chemists looking to optimize reaction conditions and improve yields. The compound's stability and reactivity profile position it as a key player in advancing research in both academic and industrial settings, providing significant advantages over similar compounds in terms of selectivity and efficiency.

Synonyms
3,4-(Ethylenedioxy)benzeneboronic acid
CAS Number
164014-95-3
Purity
97 - 105% (Assay by titration)
Molecular Formula
C8H9BO4
Molecular Weight
179.97
MDL Number
MFCD01009696
PubChem ID
2776178
Melting Point
118 °C (Lit.)
Appearance
White to almost white crystalline powder
Conditions
Store at RT
General Information
Synonyms
3,4-(Ethylenedioxy)benzeneboronic acid
CAS Number
164014-95-3
Purity
97 - 105% (Assay by titration)
Molecular Formula
C8H9BO4
Molecular Weight
179.97
MDL Number
MFCD01009696
PubChem ID
2776178
Melting Point
118 °C (Lit.)
Appearance
White to almost 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

1,4-Benzodioxane-6-boronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Drug Development: It plays a crucial role in medicinal chemistry, where it is used to create boron-containing compounds that can enhance the efficacy of drug candidates, particularly in cancer therapy.
  • Material Science: The compound is employed in the production of advanced materials, including polymers and nanomaterials, which can exhibit unique properties beneficial for electronics and coatings.
  • Bioconjugation: It is utilized in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, facilitating the development of targeted drug delivery systems.
  • Analytical Chemistry: This chemical is used in various analytical methods, including chromatography and spectroscopy, to improve the detection and quantification of specific analytes in complex mixtures.

Citations