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Catalog Number:
40148
CAS Number:
845551-44-2
Ácido 4-benciloxi-3-clorofenilborónico
Purity:
≥ 98 % (HPLC)
Synonym(s):
Ácido 4-benciloxi-3-clorobencenoborónico
Documents
$62.59 /1G
Tamaño
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Product Information

4-Benzyloxy-3-chlorophenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its unique structure, featuring a chlorophenyl group and a benzyloxy moiety, enhances its reactivity and selectivity, allowing for the development of targeted compounds with improved efficacy.

Researchers and industry professionals can leverage 4-Benzyloxy-3-chlorophenylboronic acid in the development of novel therapeutic agents, particularly in the field of cancer research, where boronic acids have shown promise in inhibiting proteasome activity. Additionally, its application in the synthesis of biologically active compounds underscores its relevance in drug discovery and development. With its favorable properties and practical applications, this compound stands out as a valuable asset for those engaged in advanced chemical research and development.

Synonyms
Ácido 4-benciloxi-3-clorobencenoborónico
CAS Number
845551-44-2
Purity
≥ 98 % (HPLC)
Molecular Formula
C13H12BClO3
Molecular Weight
262.5
MDL Number
MFCD04115642
PubChem ID
3763657
Melting Point
193 °C (Literatura)
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Tienda en RT
General Information
Synonyms
Ácido 4-benciloxi-3-clorobencenoborónico
CAS Number
845551-44-2
Purity
≥ 98 % (HPLC)
Molecular Formula
C13H12BClO3
Molecular Weight
262.5
MDL Number
MFCD04115642
PubChem ID
3763657
Melting Point
193 °C (Literatura)
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Tienda en RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-Benzyloxy-3-chlorophenylboronic acid is widely utilized in research focused on:

  • Synthetic Chemistry: This compound serves as a versatile building block in organic synthesis, particularly in the formation of complex molecules through Suzuki-Miyaura coupling reactions.
  • Pharmaceutical Development: It plays a crucial role in the development of new pharmaceuticals, especially in creating compounds that target specific biological pathways, enhancing drug efficacy.
  • Material Science: The compound is used in the design of advanced materials, including polymers and nanomaterials, which can exhibit unique electrical and optical properties.
  • Bioconjugation: It is employed in bioconjugation techniques to attach biomolecules to surfaces or other molecules, facilitating the development of biosensors and targeted drug delivery systems.
  • Research in Catalysis: This chemical is significant in catalysis research, where it aids in the development of more efficient catalytic systems that can lower energy requirements and improve reaction rates.

Citas