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Catalog Number:
39988
CAS Number:
685103-98-4
4-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)isoquinoléine
Purity:
≥ 98% (CG)
Synonym(s):
2-(4-isoquinolyl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane, Ester pinacol d'acide isoquinoléine-4-boronique
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Product Information

4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)isoquinoline is a versatile compound recognized for its unique boron-containing structure, which enhances its reactivity and stability in various chemical applications. This compound is particularly valuable in organic synthesis, where it serves as a key intermediate in the development of pharmaceuticals and agrochemicals. Its ability to participate in cross-coupling reactions makes it an essential reagent for creating complex molecular architectures, allowing researchers to explore new therapeutic avenues and optimize existing compounds.

Additionally, the presence of the dioxaborolane moiety in its structure provides unique properties that facilitate the formation of carbon-boron bonds, which are crucial in the synthesis of boron-containing compounds. This feature not only broadens the scope of potential applications but also offers advantages over traditional reagents, such as improved selectivity and reduced by-product formation. Researchers and industry professionals can leverage this compound to enhance their synthetic strategies, ultimately leading to more efficient and innovative solutions in drug discovery and materials science.

Synonyms
2-(4-isoquinolyl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane, Ester pinacol d'acide isoquinoléine-4-boronique
CAS Number
685103-98-4
Purity
≥ 98% (CG)
Molecular Formula
C 15 H 18 BNO 2
Molecular Weight
255.12
MDL Number
MFCD05663891
PubChem ID
2760594
Melting Point
99 - 103 ?C
Appearance
Poudre cristalline blanche à jaune clair
Conditions
Magasin chez RT
General Information
Synonyms
2-(4-isoquinolyl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane, Ester pinacol d'acide isoquinoléine-4-boronique
CAS Number
685103-98-4
Purity
≥ 98% (CG)
Molecular Formula
C 15 H 18 BNO 2
Molecular Weight
255.12
MDL Number
MFCD05663891
PubChem ID
2760594
Melting Point
99 - 103 ?C
Appearance
Poudre cristalline blanche à jaune clair
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)isoquinoline is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of complex organic molecules, particularly in the pharmaceutical industry, where it can aid in the development of new drugs.
  • Fluorescent Probes: It is used to create fluorescent probes for biological imaging, allowing researchers to visualize cellular processes in real-time, which is crucial for drug discovery and development.
  • Catalysis: The compound acts as a ligand in catalytic reactions, enhancing the efficiency of chemical transformations, which is beneficial in both academic and industrial settings.
  • Material Science: It finds applications in the development of advanced materials, such as polymers and nanomaterials, which are essential in electronics and nanotechnology.
  • Environmental Chemistry: This chemical can be utilized in the detection and remediation of environmental pollutants, helping industries comply with regulatory standards and improve sustainability practices.

Citations