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Catalog Number:
26366
CAS Number:
1189746-27-7
Éster de pinacol del ácido 2-metillindazol-5-borónico
Purity:
≥ 96 % (HPLC)
Synonym(s):
2-Metil-5-(4,4,5,5-tetrametil-1,3,2-dioxaborolan-2-il) -2H- indazol
Documents
$103.56 /100 mg
Tamaño
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Product Information

2-Methylindazole-5-boronic acid pinacol ester is a versatile compound that plays a significant role 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 complex organic molecules. Its unique structure allows for the introduction of various functional groups, enabling researchers to explore a wide range of chemical transformations. The compound is also recognized for its potential applications in the development of pharmaceuticals, agrochemicals, and advanced materials, where precision and efficiency are paramount.

In addition to its synthetic utility, 2-Methylindazole-5-boronic acid pinacol ester exhibits favorable properties that enhance its performance in various applications. Its stability under different conditions and compatibility with diverse reaction environments make it an attractive choice for both academic and industrial laboratories. Researchers can leverage this compound to streamline their synthesis processes, reduce waste, and improve yields, ultimately accelerating the development of innovative solutions in their respective fields.

Synonyms
2-Metil-5-(4,4,5,5-tetrametil-1,3,2-dioxaborolan-2-il) -2H- indazol
CAS Number
1189746-27-7
Purity
≥ 96 % (HPLC)
Molecular Formula
C14H19BN2O2
Molecular Weight
258.13
MDL Number
MFCD11109436
PubChem ID
44118253
Appearance
Sólido blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
2-Metil-5-(4,4,5,5-tetrametil-1,3,2-dioxaborolan-2-il) -2H- indazol
CAS Number
1189746-27-7
Purity
≥ 96 % (HPLC)
Molecular Formula
C14H19BN2O2
Molecular Weight
258.13
MDL Number
MFCD11109436
PubChem ID
44118253
Appearance
Sólido blanco
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-Methylindazole-5-boronic acid pinacol ester is widely utilized in research focused on:

  • Drug Development: This compound serves as a crucial building block in the synthesis of pharmaceuticals, particularly in developing new anti-cancer agents. Its unique boronic acid functionality allows for the formation of stable complexes with biomolecules.
  • Organic Synthesis: It is employed in various organic reactions, including Suzuki coupling, which is essential for creating complex organic molecules. This application is particularly valuable in the production of agrochemicals and fine chemicals.
  • Material Science: The compound is used in the development of advanced materials, such as polymers and nanomaterials, due to its ability to modify surface properties and enhance material performance.
  • Bioconjugation: In biochemistry, it plays a role in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, which is vital for drug delivery systems and diagnostic applications.
  • Fluorescent Probes: It can be utilized in creating fluorescent probes for biological imaging, enabling researchers to visualize cellular processes in real-time, which is crucial for understanding disease mechanisms.

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