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Catalog Number:
18105
CAS Number:
943153-22-8
Ácido 5-cloro-2-metoxipiridin-3-il)borónico
Purity:
≥ 99 % (HPLC)
Synonym(s):
Ácido 5-cloro-2-metoxi-piridina-3-borónico
Documents
$74.81 /100 mg
Tamaño
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Product Information

(5-Chloro-2-methoxypyridin-3-yl)boronic acid is a versatile boronic acid derivative known for its significant role in organic synthesis and medicinal chemistry. This compound is particularly valuable in the development of pharmaceuticals, where it serves as a key intermediate in the synthesis of various biologically active molecules. Its unique structure allows for the formation of stable complexes with diols, making it an essential reagent in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is widely utilized in the creation of complex organic frameworks.

In addition to its applications in drug discovery, (5-Chloro-2-methoxypyridin-3-yl)boronic acid is also employed in the development of agrochemicals and materials science. Its ability to facilitate the formation of carbon-carbon bonds enhances its utility in creating novel compounds with desirable properties. Researchers and industry professionals will appreciate its effectiveness in enhancing reaction yields and selectivity, making it a preferred choice in various synthetic pathways.

Synonyms
Ácido 5-cloro-2-metoxi-piridina-3-borónico
CAS Number
943153-22-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C6H7BClNO3
Molecular Weight
187.39
MDL Number
MFCD04114579
PubChem ID
44754881
Melting Point
148-152 ?C.
Appearance
Sólido blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Ácido 5-cloro-2-metoxi-piridina-3-borónico
CAS Number
943153-22-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C6H7BClNO3
Molecular Weight
187.39
MDL Number
MFCD04114579
PubChem ID
44754881
Melting Point
148-152 ?C.
Appearance
Sólido blanco
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-methoxypyridin-3-yl)boronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an important building block in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting cancer and other diseases.
  • Organic Synthesis: It is frequently used in cross-coupling reactions, which are essential in creating complex organic molecules, making it valuable for researchers in organic chemistry.
  • Material Science: The compound is applied in the development of new materials, such as polymers and coatings, enhancing properties like durability and resistance to environmental factors.
  • Agricultural Chemistry: It plays a role in the formulation of agrochemicals, contributing to the development of effective herbicides and pesticides that are safer for the environment.
  • Analytical Chemistry: Utilized in various analytical techniques, it helps in the detection and quantification of specific compounds, aiding researchers in environmental and food safety studies.

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