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Catalog Number:
28741
CAS Number:
145349-62-8
2-Chloro-4-methylphenylboronic acid
Purity:
≥ 98%
Documents
$18.53 /1G
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Product Information

2-Chloro-4-methylphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Researchers and industry professionals leverage its unique properties to create complex organic molecules, including pharmaceuticals and agrochemicals. Its application extends to the development of advanced materials and sensors, where its boron functionality plays a critical role in enhancing performance and stability.

The compound's distinctive chloromethyl group enhances its reactivity, allowing for efficient functionalization in various chemical transformations. This makes 2-Chloro-4-methylphenylboronic acid a preferred choice for those looking to streamline their synthetic pathways while achieving high yields. With its broad applicability and significant advantages over similar compounds, it stands out as a valuable tool for chemists aiming to innovate in their respective fields.

CAS Number
145349-62-8
Purity
≥ 98%
Molecular Formula
C7H8BClO2
Molecular Weight
170.4
MDL Number
MFCD03411936
PubChem ID
2773334
Appearance
White to off-white powder
Conditions
Store at 0-8°C
General Information
CAS Number
145349-62-8
Purity
≥ 98%
Molecular Formula
C7H8BClO2
Molecular Weight
170.4
MDL Number
MFCD03411936
PubChem ID
2773334
Appearance
White to off-white powder
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-Chloro-4-methylphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Cross-Coupling Reactions: It plays a crucial role in Suzuki-Miyaura coupling reactions, allowing for the formation of carbon-carbon bonds, which is essential in creating complex organic structures.
  • Material Science: The compound is used in the development of advanced materials, including polymers and nanomaterials, due to its ability to modify surface properties and enhance material performance.
  • Bioconjugation: It is utilized in bioconjugation techniques to attach biomolecules to surfaces or other molecules, facilitating applications in drug delivery and diagnostic assays.
  • Chemical Sensors: This chemical is employed in the fabrication of chemical sensors, which can detect specific analytes, making it valuable in environmental monitoring and safety applications.

Citations