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Catalog Number:
40240
CAS Number:
851335-09-6
Ácido 4-carboxi-2-clorofenilborónico
Purity:
98 - 105% (Ensayo por titulación)
Synonym(s):
Ácido 4-carboxi-2-clorobencenoborónico
Documents
$100.05 /1G
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Product Information

4-Carboxy-2-chlorophenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative features a carboxylic acid group and a chlorophenyl moiety, making it an essential building block for the development of pharmaceuticals and agrochemicals. Its unique ability to form reversible covalent bonds with diols allows for applications in drug delivery systems and the design of targeted therapies. Researchers have leveraged its properties in the synthesis of complex molecules, including those used in cancer treatment and other therapeutic areas.

Additionally, 4-Carboxy-2-chlorophenylboronic acid serves as a crucial reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the production of advanced materials and fine chemicals. Its compatibility with various substrates and functional groups enhances its utility in diverse chemical transformations. With its robust performance in both academic and industrial settings, this compound stands out as a key player in the advancement of modern chemistry.

Synonyms
Ácido 4-carboxi-2-clorobencenoborónico
CAS Number
851335-09-6
Purity
98 - 105% (Ensayo por titulación)
Molecular Formula
C7H6BClO4
Molecular Weight
200.38
MDL Number
MFCD07363763
PubChem ID
17750227
Melting Point
210 °C (Literatura)
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Tienda en RT
General Information
Synonyms
Ácido 4-carboxi-2-clorobencenoborónico
CAS Number
851335-09-6
Purity
98 - 105% (Ensayo por titulación)
Molecular Formula
C7H6BClO4
Molecular Weight
200.38
MDL Number
MFCD07363763
PubChem ID
17750227
Melting Point
210 °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-Carboxy-2-chlorophenylboronic acid is widely utilized in research focused on:

  • Drug Development: This compound serves as a key intermediate in synthesizing various pharmaceuticals, particularly in the development of cancer therapies that target specific cellular pathways.
  • Bioconjugation: It is employed in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing the effectiveness of drug delivery systems.
  • Organic Synthesis: The compound is a valuable reagent in organic synthesis, facilitating the formation of carbon-carbon bonds, which is crucial in creating complex organic molecules.
  • Sensor Technology: It is used in the development of chemical sensors for detecting specific analytes, benefiting industries such as environmental monitoring and food safety.
  • Material Science: This chemical plays a role in creating advanced materials, including polymers and nanomaterials, which are essential in electronics and renewable energy applications.

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