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Catalog Number:
40261
CAS Number:
603122-80-1
2-Chloro-4-(methoxycarbonyl)phenylboronic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
2-Chloro-4-(methoxycarbonyl)benzeneboronic acid
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Product Information

2-Chloro-4-(methoxycarbonyl)phenylboronic 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 participate in Suzuki-Miyaura cross-coupling reactions, making it invaluable for the formation of carbon-carbon bonds. Its unique structure, featuring a chloro substituent and a methoxycarbonyl group, enhances its reactivity and selectivity, allowing researchers to create complex molecules with precision.

In pharmaceutical development, 2-Chloro-4-(methoxycarbonyl)phenylboronic acid is utilized in the synthesis of various biologically active compounds, including potential drug candidates. Its applications extend to the production of agrochemicals and materials science, where it aids in the development of novel polymers and functional materials. The compound's ability to facilitate efficient coupling reactions positions it as a preferred choice for chemists seeking reliable and effective building blocks in their synthetic pathways.

Synonyms
2-Chloro-4-(methoxycarbonyl)benzeneboronic acid
CAS Number
603122-80-1
Purity
≥ 98% (HPLC)
Molecular Formula
C8H8BClO4
Molecular Weight
214.41
MDL Number
MFCD08689530
PubChem ID
22171291
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
2-Chloro-4-(methoxycarbonyl)benzeneboronic acid
CAS Number
603122-80-1
Purity
≥ 98% (HPLC)
Molecular Formula
C8H8BClO4
Molecular Weight
214.41
MDL Number
MFCD08689530
PubChem ID
22171291
Appearance
White to off-white crystalline powder
Conditions
Store at RT
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-(methoxycarbonyl)phenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound is crucial in synthesizing various pharmaceuticals, particularly in creating targeted therapies for cancer treatment. Its boronic acid functionality allows for the formation of stable complexes with biomolecules.
  • Organic Synthesis: It serves as an important building block in organic synthesis, facilitating the creation of complex organic molecules through Suzuki coupling reactions, which are essential in developing new materials and drugs.
  • Material Science: The compound is used in the production of advanced materials, such as polymers and nanomaterials, enhancing properties like conductivity and strength, which are vital in electronics and construction.
  • Agricultural Chemistry: It finds applications in developing agrochemicals, contributing to the design of herbicides and pesticides that are more effective and environmentally friendly, thus supporting sustainable agriculture.
  • Bioconjugation: This chemical is utilized in bioconjugation processes, linking biomolecules for diagnostics and therapeutic applications, providing a means to improve the specificity and efficacy of treatments.

Citations