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Catalog Number:
40160
CAS Number:
98546-51-1
Acide 4-(méthylthio)phénylboronique
Purity:
95 - 105 % (dosage par titrage)
Synonym(s):
Acide 4-(méthylthio)benzèneboronique
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Product Information

4-(Methylthio)phenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized 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 develop pharmaceuticals, agrochemicals, and advanced materials. Its application extends to the synthesis of biologically active compounds, where it plays a crucial role in the formation of carbon-carbon bonds, enhancing the efficiency of synthetic pathways.

In addition to its synthetic utility, 4-(Methylthio)phenylboronic acid is also valuable in the development of sensors and diagnostic tools due to its reactivity with specific biomolecules. Its ability to selectively bind to certain targets allows for the creation of sensitive detection methods, which are vital in various research fields, including biochemistry and environmental science. With its broad range of applications and benefits, this compound stands out as a key player in modern chemical research and development.

Synonyms
Acide 4-(méthylthio)benzèneboronique
CAS Number
98546-51-1
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C 7 H 9 B O 2 S
Molecular Weight
168.02
MDL Number
MFCD00093410
PubChem ID
2733959
Melting Point
213 °C (lit.)
Appearance
Poudre cristalline blanche à orange
Conditions
Magasin chez RT
General Information
Synonyms
Acide 4-(méthylthio)benzèneboronique
CAS Number
98546-51-1
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C 7 H 9 B O 2 S
Molecular Weight
168.02
MDL Number
MFCD00093410
PubChem ID
2733959
Melting Point
213 °C (lit.)
Appearance
Poudre cristalline blanche à orange
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

4-(Methylthio)phenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key reagent in Suzuki-Miyaura cross-coupling reactions, allowing chemists to create complex organic molecules efficiently. Its ability to form stable complexes with various substrates enhances reaction yields.
  • Pharmaceutical Development: It plays a crucial role in the synthesis of biologically active compounds, particularly in the development of new drugs. Researchers can modify its structure to improve the efficacy and selectivity of potential pharmaceuticals.
  • Material Science: The compound is used in the creation of advanced materials, such as polymers and nanomaterials, which can be tailored for specific applications like sensors or drug delivery systems, offering enhanced performance over traditional materials.
  • Bioconjugation: It is employed in bioconjugation techniques to attach biomolecules to surfaces or other molecules, facilitating the development of targeted therapies and diagnostic tools in the biomedical field.
  • Environmental Chemistry: The compound is utilized in the detection and removal of pollutants, particularly in water treatment processes, showcasing its versatility and effectiveness in addressing environmental challenges.

Citations