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Catalog Number:
40232
CAS Number:
874219-45-1
4-Chloro-3-(methoxycarbonyl)phenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
4-Chloro-3-(methoxycarbonyl)benzeneboronic acid
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$49.67 /200MG
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Product Information

4-Chloro-3-(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 an essential building block for the formation of biaryl compounds, which are significant in pharmaceuticals and agrochemicals. Its unique structure allows for the introduction of various functional groups, enhancing the diversity of synthesized compounds. Researchers and industry professionals can leverage this compound in the development of new drugs, particularly in the synthesis of anti-cancer agents and other therapeutic molecules.

Additionally, 4-Chloro-3-(methoxycarbonyl)phenylboronic acid exhibits excellent solubility in organic solvents, facilitating its use in various reaction conditions. Its stability and reactivity make it a preferred choice for chemists looking to streamline their synthesis processes. With its broad applicability in both academic research and industrial applications, this compound stands out as a valuable asset for those engaged in the fields of organic chemistry and pharmaceuticals.

Synonyms
4-Chloro-3-(methoxycarbonyl)benzeneboronic acid
CAS Number
874219-45-1
Purity
97 - 105% (Assay by titration)
Molecular Formula
C8H8BClO4
Molecular Weight
214.41
MDL Number
MFCD06801690
PubChem ID
23005334
Melting Point
138 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
4-Chloro-3-(methoxycarbonyl)benzeneboronic acid
CAS Number
874219-45-1
Purity
97 - 105% (Assay by titration)
Molecular Formula
C8H8BClO4
Molecular Weight
214.41
MDL Number
MFCD06801690
PubChem ID
23005334
Melting Point
138 °C (Lit.)
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

4-Chloro-3-(methoxycarbonyl)phenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound is instrumental in the synthesis of various pharmaceuticals, particularly in the development of targeted cancer therapies due to its ability to form stable complexes with biologically relevant molecules.
  • Organic Synthesis: It serves as a key intermediate in organic synthesis, allowing chemists to create complex molecules efficiently. Its unique structure enables the formation of diverse chemical bonds, enhancing synthetic pathways.
  • Material Science: In the field of material science, it is used to modify polymer properties, improving their mechanical strength and thermal stability, which is essential for developing advanced materials.
  • Bioconjugation: The compound is valuable in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, facilitating the development of biosensors and diagnostic tools.
  • Environmental Chemistry: It plays a role in environmental applications, such as the detection and removal of pollutants, by forming complexes with harmful substances, thus aiding in environmental remediation efforts.

Citations