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Catalog Number:
18106
CAS Number:
475275-69-5
Ácido 5-cloro-2-metoxi-piridina-4-borónico
Purity:
≥ 95 % (HPLC)
Synonym(s):
Ácido (5-cloro-2-metoxipiridin-4-il)borónico
Documents
$72.31 /250 mg
Tamaño
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Product Information

5-Chloro-2-methoxy-pyridine-4-boronic acid is a versatile boronic acid derivative that plays a crucial role in various chemical synthesis applications, particularly in the pharmaceutical and agrochemical industries. This compound is recognized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the synthesis of complex organic molecules. Its unique structure, featuring a chloro and methoxy group, enhances its reactivity and selectivity, allowing for the efficient formation of carbon-carbon bonds. Researchers and industry professionals can leverage this compound to develop novel pharmaceuticals, agrochemicals, and advanced materials, significantly streamlining their synthesis processes.

In addition to its synthetic utility, 5-Chloro-2-methoxy-pyridine-4-boronic acid exhibits favorable solubility characteristics, which facilitate its use in various reaction conditions. Its compatibility with a wide range of substrates makes it an attractive option for chemists looking to optimize their reaction conditions. This compound not only enhances the efficiency of chemical reactions but also contributes to the development of innovative solutions in drug discovery and material science.

Synonyms
Ácido (5-cloro-2-metoxipiridin-4-il)borónico
CAS Number
475275-69-5
Purity
≥ 95 % (HPLC)
Molecular Formula
C6H7BClNO3
Molecular Weight
187.39
MDL Number
MFCD06658398
PubChem ID
11030558
Appearance
Polvo blanquecino
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Ácido (5-cloro-2-metoxipiridin-4-il)borónico
CAS Number
475275-69-5
Purity
≥ 95 % (HPLC)
Molecular Formula
C6H7BClNO3
Molecular Weight
187.39
MDL Number
MFCD06658398
PubChem ID
11030558
Appearance
Polvo blanquecino
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

5-Chloro-2-methoxy-pyridine-4-boronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-cancer agents. Its boronic acid functionality allows for the formation of stable complexes with biomolecules, enhancing drug efficacy.
  • Organic Synthesis: It is employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, which are essential for creating complex organic molecules. This application is crucial in the production of agrochemicals and fine chemicals.
  • Material Science: The compound is used in the development of advanced materials, including polymers and coatings. Its unique properties contribute to the creation of materials with improved durability and chemical resistance.
  • Bioconjugation: In biochemistry, it is utilized for labeling biomolecules, aiding in the study of protein interactions and cellular processes. This application is vital for researchers in the fields of molecular biology and biochemistry.
  • Environmental Chemistry: It plays a role in the development of sensors for detecting environmental pollutants. Its ability to form selective complexes makes it useful in monitoring applications, contributing to environmental protection efforts.

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