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Catalog Number:
40114
CAS Number:
121219-12-3
Acide 4-amylphénylboronique
Purity:
95 - 105 % (dosage par titrage)
Synonym(s):
Acide 4-amylbenzèneboronique, Acide 4-pentylphénylboronique, Acide 4-pentylbenzèneboronique
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Product Information

4-Amylphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative features a pentyl group that enhances its solubility and reactivity, making it an excellent candidate for various applications. It is particularly valuable in the development of pharmaceuticals, where it serves as a key building block in the synthesis of biologically active compounds. Researchers often leverage its ability to form reversible covalent bonds with diols, which is crucial in the design of sensors and drug delivery systems.

In addition to its role in drug development, 4-Amylphenylboronic acid is also employed in materials science, particularly in the creation of polymers and nanomaterials. Its unique properties facilitate the formation of complex structures that can be tailored for specific applications, such as in catalysis and environmental remediation. The compound's stability and reactivity make it a preferred choice for professionals seeking reliable and effective solutions in their research and industrial processes.

Synonyms
Acide 4-amylbenzèneboronique, Acide 4-pentylphénylboronique, Acide 4-pentylbenzèneboronique
CAS Number
121219-12-3
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C 11 H 17 BO 2
Molecular Weight
192.07
MDL Number
MFCD00995151
PubChem ID
4589191
Melting Point
84 °C (lit.)
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Magasin chez RT
General Information
Synonyms
Acide 4-amylbenzèneboronique, Acide 4-pentylphénylboronique, Acide 4-pentylbenzèneboronique
CAS Number
121219-12-3
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C 11 H 17 BO 2
Molecular Weight
192.07
MDL Number
MFCD00995151
PubChem ID
4589191
Melting Point
84 °C (lit.)
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

4-Amylphenylboronic acid is widely utilized in research focused on:

  • Drug Development: This compound is used in the synthesis of boronic acid derivatives, which play a crucial role in developing pharmaceuticals, particularly in targeting cancer cells.
  • Organic Synthesis: It serves as a key reagent in Suzuki coupling reactions, allowing chemists to create complex organic molecules efficiently, which is essential in materials science and agrochemicals.
  • Bioconjugation: The ability to form stable bonds with biomolecules makes it valuable for creating bioconjugates, enhancing drug delivery systems and diagnostic tools in the biomedical field.
  • Sensor Technology: Its properties are exploited in developing sensors for detecting glucose levels, providing a practical application in diabetes management and monitoring.
  • Polymer Chemistry: It is used in the modification of polymers, improving their properties for applications in coatings, adhesives, and other materials, thus enhancing performance and durability.

Citations