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Catalog Number:
40070
CAS Number:
4737-50-2
Ácido pentilborónico
Purity:
97 - 105% (Ensayo por titulación)
Synonym(s):
Ácido 1-pentanoborónico
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Product Information

Pentylboronic acid is a versatile organoboron compound recognized for its utility in organic synthesis and medicinal chemistry. This compound features a pentyl group attached to a boronic acid functional group, making it an essential reagent for the formation of carbon-carbon bonds through Suzuki-Miyaura cross-coupling reactions. Its ability to act as a boron source allows for the development of complex molecules, which is particularly valuable in the pharmaceutical industry for drug discovery and development. Additionally, pentylboronic acid can be utilized in the preparation of various polymers and materials, enhancing their properties and functionalities.

Researchers and industry professionals appreciate pentylboronic acid for its unique reactivity and compatibility with a wide range of substrates. Its application extends to the synthesis of biologically active compounds, where it serves as a building block for creating novel therapeutic agents. The compound's stability and ease of handling further contribute to its appeal, making it a preferred choice in laboratories focused on innovative chemical research and development.

Synonyms
Ácido 1-pentanoborónico
CAS Number
4737-50-2
Purity
97 - 105% (Ensayo por titulación)
Molecular Formula
C5H13BO2
Molecular Weight
115.97
MDL Number
MFCD01074651
PubChem ID
352103
Melting Point
94 °C (Literatura)
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Conservar a ≤ -10 °C
General Information
Synonyms
Ácido 1-pentanoborónico
CAS Number
4737-50-2
Purity
97 - 105% (Ensayo por titulación)
Molecular Formula
C5H13BO2
Molecular Weight
115.97
MDL Number
MFCD01074651
PubChem ID
352103
Melting Point
94 °C (Literatura)
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Conservar a ≤ -10 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Pentylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: It serves as a crucial building block in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Cross-Coupling Reactions: This compound is essential in Suzuki-Miyaura coupling reactions, allowing chemists to create carbon-carbon bonds efficiently, which is vital in creating diverse organic compounds.
  • Bioconjugation: It is used in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, enhancing drug delivery systems and diagnostic tools.
  • Material Science: Pentylboronic acid plays a role in the development of new materials, such as polymers and nanomaterials, which have applications in electronics and coatings.
  • Sensor Development: Its unique properties make it suitable for the creation of sensors that detect specific biomolecules, contributing to advancements in medical diagnostics and environmental monitoring.

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