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Catalog Number:
40161
CAS Number:
128312-11-8
3-(Methylthio)phenylboronic acid
Purity:
≥ 95% (Assay by titration)
Synonym(s):
3-(Methylthio)benzeneboronic acid
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Product Information

3-(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 in the synthesis of biologically active compounds highlights its significance in drug discovery and development, particularly in creating targeted therapies.

Moreover, 3-(Methylthio)phenylboronic acid serves as a valuable building block in the synthesis of functionalized polymers and materials, enhancing the performance characteristics of various products. Its ease of use and compatibility with a range of reaction conditions make it a preferred choice for chemists seeking reliable and efficient solutions. With its potential to streamline synthetic pathways and improve yields, this compound stands out as a key player in modern chemical research and industrial applications.

Synonyms
3-(Methylthio)benzeneboronic acid
CAS Number
128312-11-8
Purity
≥ 95% (Assay by titration)
Molecular Formula
C7H9BO2S
Molecular Weight
168.02
MDL Number
MFCD01319105
PubChem ID
2734383
Melting Point
162 °C (Lit.)
Appearance
White to light yellow crystalline powder
Conditions
Store at RT
General Information
Synonyms
3-(Methylthio)benzeneboronic acid
CAS Number
128312-11-8
Purity
≥ 95% (Assay by titration)
Molecular Formula
C7H9BO2S
Molecular Weight
168.02
MDL Number
MFCD01319105
PubChem ID
2734383
Melting Point
162 °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

3-(Methylthio)phenylboronic 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 is extensively used in Suzuki-Miyaura coupling reactions, which are crucial for forming carbon-carbon bonds in complex organic compounds, enhancing efficiency in drug development.
  • Bioconjugation: The ability to form stable bonds with biomolecules makes it valuable in bioconjugation processes, aiding in the development of targeted drug delivery systems.
  • Material Science: In the production of functional materials, it contributes to the development of sensors and electronic devices, leveraging its unique chemical properties.
  • Analytical Chemistry: It is used in the preparation of analytical standards and reagents, facilitating accurate measurements and analyses in various chemical assessments.

Citations