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Catalog Number:
39907
CAS Number:
68716-52-9
4,4,5,5-Tetramethyl-2-(1-naphthyl)-1,3,2-dioxaborolane
Purity:
≥ 98% (GC)
Synonym(s):
Naphthalene-1-boronic acid pinacol ester, 1-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalene
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Product Information

4,4,5,5-Tetramethyl-2-(1-naphthyl)-1,3,2-dioxaborolane is a specialized boron-containing compound that has garnered attention in various fields, particularly in organic synthesis and materials science. This compound is recognized for its unique ability to act as a versatile building block in the synthesis of complex organic molecules, making it invaluable for researchers engaged in the development of pharmaceuticals and agrochemicals. Its structure allows for easy incorporation into various chemical reactions, enhancing the efficiency of synthetic pathways.

Moreover, 4,4,5,5-Tetramethyl-2-(1-naphthyl)-1,3,2-dioxaborolane exhibits excellent stability and solubility characteristics, which are crucial for applications in catalysis and polymer chemistry. Researchers have utilized this compound in the preparation of functionalized naphthalene derivatives, which are essential in the production of dyes, pigments, and advanced materials. Its unique properties not only streamline synthetic processes but also improve yields, making it a preferred choice for professionals seeking reliable and effective reagents in their work.

Synonyms
Naphthalene-1-boronic acid pinacol ester, 1-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalene
CAS Number
68716-52-9
Purity
≥ 98% (GC)
Molecular Formula
C16H19BO2
Molecular Weight
254.14
MDL Number
MFCD05663869
PubChem ID
2760174
Melting Point
55 - 59 ?C
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
Naphthalene-1-boronic acid pinacol ester, 1-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalene
CAS Number
68716-52-9
Purity
≥ 98% (GC)
Molecular Formula
C16H19BO2
Molecular Weight
254.14
MDL Number
MFCD05663869
PubChem ID
2760174
Melting Point
55 - 59 ?C
Appearance
White to off-white 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

4,4,5,5-Tetramethyl-2-(1-naphthyl)-1,3,2-dioxaborolane is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile reagent in organic chemistry, particularly in the synthesis of complex molecules, allowing chemists to create desired structures with precision.
  • Pharmaceutical Development: It is used in drug discovery processes, helping researchers modify and optimize drug candidates, which can lead to more effective treatments with fewer side effects.
  • Materials Science: The compound plays a role in developing advanced materials, such as polymers and coatings, enhancing their properties like durability and resistance to environmental factors.
  • Bioconjugation: In biochemistry, it is employed for labeling biomolecules, aiding in the study of biological processes and the development of diagnostic tools.
  • Fluorescent Probes: This chemical is also utilized in creating fluorescent probes for imaging applications, providing researchers with powerful tools for visualizing cellular processes in real-time.

Citations