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Catalog Number:
19757
CAS Number:
1251537-48-0
1-Benzyl-piperidine-4-boronic acid
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Product Information

1-Benzyl-piperidine-4-boronic acid is a versatile compound that plays a significant role in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its utility in the development of various pharmaceuticals, particularly in the synthesis of biologically active compounds. Its unique structure allows for the formation of stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. This property is particularly valuable in the creation of complex molecules, including agrochemicals and fine chemicals, where precision and efficiency are paramount.

Researchers and industry professionals can leverage 1-Benzyl-piperidine-4-boronic acid in drug discovery and development processes, as it facilitates the construction of intricate molecular architectures. Its ability to enhance the solubility and bioavailability of compounds makes it a preferred choice in pharmaceutical formulations. With its growing importance in the synthesis of targeted therapies, this compound stands out for its effectiveness and adaptability in various applications, ensuring that it meets the evolving needs of the chemical and pharmaceutical industries.

CAS Number
1251537-48-0
Molecular Formula
C12H18BNO2
Molecular Weight
219.09
MDL Number
MFCD07371553
PubChem ID
46941045
Conditions
Store at 0-8°C
General Information
CAS Number
1251537-48-0
Molecular Formula
C12H18BNO2
Molecular Weight
219.09
MDL Number
MFCD07371553
PubChem ID
46941045
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

1-Benzyl-piperidine-4-boronic acid is widely utilized in research focused on:

  • Drug Development: This compound serves as a crucial intermediate in synthesizing various pharmaceuticals, particularly in developing drugs targeting neurological disorders.
  • Chemical Synthesis: It acts as a versatile building block in organic synthesis, allowing chemists to create complex molecules efficiently, which is essential in both academic and industrial settings.
  • Bioconjugation: The boronic acid group can form reversible covalent bonds with diols, making it useful for bioconjugation techniques in creating targeted drug delivery systems.
  • Material Science: It is employed in the development of advanced materials, including polymers and coatings, due to its ability to enhance material properties through boron chemistry.
  • Analytical Chemistry: This compound is used in various analytical methods, such as chromatography, to improve the detection and separation of biomolecules, aiding researchers in their studies.

Citations