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Catalog Number:
40143
CAS Number:
380427-38-3
4-(Isopropylthio)phenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
4-(Isopropylthio)benzeneboronic acid
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Product Information

4-(Isopropylthio)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. Its unique isopropylthio group enhances its reactivity and selectivity, enabling researchers to develop complex organic molecules with precision. This compound is particularly valuable in the synthesis of pharmaceuticals and agrochemicals, where it aids in the construction of carbon-carbon bonds, facilitating the development of new therapeutic agents and crop protection products.

In addition to its synthetic applications, 4-(Isopropylthio)phenylboronic acid has shown potential in the field of materials science, where it can be employed in the creation of functionalized polymers and advanced materials. Its ability to act as a building block in various chemical transformations opens up opportunities for innovation in drug discovery and material development. Researchers and industry professionals can leverage this compound's properties to enhance their projects, streamline synthesis processes, and explore new avenues in their respective fields.

Synonyms
4-(Isopropylthio)benzeneboronic acid
CAS Number
380427-38-3
Purity
97 - 105% (Assay by titration)
Molecular Formula
C9H13BO2S
Molecular Weight
196.07
MDL Number
MFCD03411947
PubChem ID
2773483
Melting Point
88 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
4-(Isopropylthio)benzeneboronic acid
CAS Number
380427-38-3
Purity
97 - 105% (Assay by titration)
Molecular Formula
C9H13BO2S
Molecular Weight
196.07
MDL Number
MFCD03411947
PubChem ID
2773483
Melting Point
88 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

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

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Chemical Sensors: It is employed in the creation of chemical sensors that detect specific biomolecules, enhancing diagnostic capabilities in medical research.
  • Drug Development: The compound plays a crucial role in the design of boron-containing drugs, which can improve the efficacy and selectivity of therapeutic agents.
  • Material Science: It is used in the development of advanced materials, including polymers and nanomaterials, which have applications in electronics and coatings.
  • Catalysis: This chemical is a key component in catalytic reactions, facilitating efficient transformations in various chemical processes, thus offering advantages over traditional catalysts.

Citations