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Catalog Number:
40170
CAS Number:
168618-42-6
2-(Methylthio)phenylboronic acid
Purity:
95 - 105% (Assay by titration)
Synonym(s):
2-(Methylthio)benzeneboronic acid
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Product Information

2-(Methylthio)phenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the formation of biaryl compounds. Its unique methylthio group enhances its reactivity and selectivity, allowing researchers to create complex molecular architectures with precision. This compound is also explored for its potential applications in the development of pharmaceuticals, agrochemicals, and advanced materials, where its ability to form stable complexes with various substrates can lead to innovative solutions in drug design and delivery.

In addition to its synthetic utility, 2-(Methylthio)phenylboronic acid exhibits promising properties that make it suitable for various applications in the fields of catalysis and materials science. Its compatibility with different reaction conditions and substrates allows for a broad range of applications, from the synthesis of functionalized polymers to the development of novel catalysts. Researchers and industry professionals can leverage this compound's unique features to enhance their projects, streamline processes, and achieve superior results in their respective fields.

Synonyms
2-(Methylthio)benzeneboronic acid
CAS Number
168618-42-6
Purity
95 - 105% (Assay by titration)
Molecular Formula
C7H9BO2S
Molecular Weight
168.02
MDL Number
MFCD01318165
PubChem ID
2773543
Melting Point
83 °C (Lit.)
Appearance
White to light yellow crystalline powder
Conditions
Store at RT
General Information
Synonyms
2-(Methylthio)benzeneboronic acid
CAS Number
168618-42-6
Purity
95 - 105% (Assay by titration)
Molecular Formula
C7H9BO2S
Molecular Weight
168.02
MDL Number
MFCD01318165
PubChem ID
2773543
Melting Point
83 °C (Lit.)
Appearance
White to light yellow 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-(Methylthio)phenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key intermediate in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals, allowing for the creation of complex structures with high specificity.
  • Cross-Coupling Reactions: It is extensively used in Suzuki-Miyaura coupling reactions, which are essential for forming carbon-carbon bonds. This application is crucial in the production of biaryl compounds that are important in materials science and medicinal chemistry.
  • Fluorescent Probes: The compound can be employed in the development of fluorescent probes for biological imaging, enhancing the ability to visualize cellular processes in real-time, which is vital for researchers in cell biology.
  • Sensor Development: Its unique properties make it suitable for creating sensors that detect specific biomolecules, providing a valuable tool in environmental monitoring and medical diagnostics.
  • Drug Development: The compound is used in the design of boron-containing drugs, which can exhibit improved pharmacological properties, offering advantages over traditional drug compounds in terms of efficacy and selectivity.

Citations