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Catalog Number:
39962
CAS Number:
1171891-31-8
4-méthyl-3-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)pyridine
Purity:
≥ 98% (CG)
Synonym(s):
Ester pinacol de l'acide 4-méthyl-3-pyridylboronique, 2-(4-méthyl-3-pyridyl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane
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Product Information

4-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a versatile compound that plays a significant role in organic synthesis and medicinal chemistry. This compound features a unique boron-containing dioxaborolane moiety, which enhances its reactivity and makes it an excellent candidate for various applications, including the development of pharmaceuticals and agrochemicals. Its structure allows for efficient coupling reactions, making it particularly valuable in the synthesis of complex organic molecules.

Researchers and industry professionals can leverage this compound for its potential in creating novel materials and intermediates. Its ability to facilitate cross-coupling reactions positions it as a key player in the synthesis of biologically active compounds, contributing to advancements in drug discovery and development. Additionally, its stability and compatibility with various reaction conditions make it a reliable choice for synthetic chemists looking to streamline their processes and improve yields.

Synonyms
Ester pinacol de l'acide 4-méthyl-3-pyridylboronique, 2-(4-méthyl-3-pyridyl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane
CAS Number
1171891-31-8
Purity
≥ 98% (CG)
Molecular Formula
C 12 H 18 BNO 2
Molecular Weight
219.09
MDL Number
MFCD12923382
PubChem ID
57370080
Melting Point
106 - 110 ?C
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Conserver à ≤ -10 °C
General Information
Synonyms
Ester pinacol de l'acide 4-méthyl-3-pyridylboronique, 2-(4-méthyl-3-pyridyl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane
CAS Number
1171891-31-8
Purity
≥ 98% (CG)
Molecular Formula
C 12 H 18 BNO 2
Molecular Weight
219.09
MDL Number
MFCD12923382
PubChem ID
57370080
Melting Point
106 - 110 ?C
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Conserver à ≤ -10 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

4-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of various organic molecules, enabling chemists to create complex structures efficiently.
  • Pharmaceutical Development: Its unique properties make it valuable in drug discovery, particularly in the design of new pharmaceuticals that target specific biological pathways.
  • Material Science: The compound is used in developing advanced materials, such as polymers and coatings, that require specific chemical properties for enhanced performance.
  • Catalysis: It acts as a ligand in catalytic processes, improving reaction rates and selectivity, which is crucial in industrial applications like fine chemical production.
  • Analytical Chemistry: This chemical is employed in various analytical techniques, aiding in the detection and quantification of substances in complex mixtures.

Citations