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Catalog Number:
26180
CAS Number:
175883-61-1
Ácido 3,5-dicloro-4-metoxifenilborónico
Purity:
≥ 95 % (HPLC)
Documents
$60.39 /100 mg
Tamaño
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Product Information

3,5-Dichloro-4-methoxyphenylboronic acid is a versatile boronic acid derivative that plays a crucial role in organic synthesis and medicinal chemistry. This compound is recognized for its ability to form stable complexes with various substrates, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Its unique structure, featuring both chlorine and methoxy groups, enhances its reactivity and selectivity, allowing researchers to create complex organic molecules with precision. This compound is particularly valuable in the development of pharmaceuticals, agrochemicals, and advanced materials, where it can facilitate the formation of carbon-carbon bonds in a variety of synthetic pathways.

In addition to its synthetic applications, 3,5-Dichloro-4-methoxyphenylboronic acid is also utilized in the preparation of fluorescent probes and sensors, contributing to advancements in analytical chemistry. Its compatibility with various functional groups and ease of handling make it a preferred choice for researchers looking to streamline their synthesis processes. With its broad range of applications and significant advantages over similar compounds, this boronic acid derivative is an indispensable tool for professionals in the fields of chemistry and materials science.

CAS Number
175883-61-1
Purity
≥ 95 % (HPLC)
Molecular Formula
C7H7BCl2O3
Molecular Weight
220.85
MDL Number
MFCD04039018
PubChem ID
4197352
Appearance
Sólido blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
175883-61-1
Purity
≥ 95 % (HPLC)
Molecular Formula
C7H7BCl2O3
Molecular Weight
220.85
MDL Number
MFCD04039018
PubChem ID
4197352
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

3,5-Dichloro-4-methoxyphenylboronic acid is widely utilized in research focused on:

  • Drug Development: This compound serves as a key intermediate in synthesizing various pharmaceuticals, particularly in developing anti-cancer agents that target specific cellular pathways.
  • Organic Synthesis: It is employed in Suzuki coupling reactions, allowing chemists to create complex organic molecules efficiently, which is crucial in materials science and agrochemicals.
  • Bioconjugation: The compound is useful in attaching biomolecules to surfaces or other molecules, enhancing the effectiveness of diagnostic tools and drug delivery systems in the biomedical field.
  • Environmental Chemistry: It can be used in the detection and analysis of environmental pollutants, providing valuable insights into contamination levels and helping in regulatory compliance.
  • Material Science: This boronic acid derivative is explored in developing new materials with unique properties, such as sensors and catalysts, which can lead to advancements in technology and manufacturing.

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