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Catalog Number:
39892
CAS Number:
78782-17-9
Bis[(pinacolato)boryl]methane
Purity:
≥ 95% (GC)
Synonym(s):
2,2'-Methylenebis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane), Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methane
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Product Information

Bis[(pinacolato)boryl]methane is a versatile organoboron compound that has garnered significant attention in the fields of organic synthesis and materials science. Known for its unique structure, this compound serves as a valuable reagent in cross-coupling reactions, particularly in the formation of carbon-carbon bonds. Its ability to act as a borylating agent makes it an essential tool for researchers looking to synthesize complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, Bis[(pinacolato)boryl]methane is utilized in the development of advanced materials, such as polymers and catalysts, due to its favorable reactivity and stability.

The compound's unique properties, including its high solubility and ease of handling, make it an attractive choice for both academic and industrial applications. Researchers have successfully employed Bis[(pinacolato)boryl]methane in various synthetic pathways, demonstrating its potential to streamline processes and enhance yields. Its role in the burgeoning field of organoboron chemistry highlights its importance in modern chemical research and development, making it a compound of choice for professionals seeking innovative solutions in synthesis and materials design.

Synonyms
2,2'-Methylenebis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane), Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methane
CAS Number
78782-17-9
Purity
≥ 95% (GC)
Molecular Formula
C13H26B2O4
Molecular Weight
267.97
MDL Number
MFCD27977747
PubChem ID
11311685
Melting Point
51 - 55 ?C
Appearance
White to off-white crystalline powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
2,2'-Methylenebis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane), Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methane
CAS Number
78782-17-9
Purity
≥ 95% (GC)
Molecular Formula
C13H26B2O4
Molecular Weight
267.97
MDL Number
MFCD27977747
PubChem ID
11311685
Melting Point
51 - 55 ?C
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

Bis[(pinacolato)boryl]methane is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile reagent in the synthesis of various organic molecules, particularly in the formation of carbon-boron bonds, which are crucial for building complex organic structures.
  • Catalysis: It is employed as a catalyst in cross-coupling reactions, enabling the efficient formation of carbon-carbon bonds. This application is particularly valuable in the pharmaceutical and agrochemical industries for developing new compounds.
  • Materials Science: The compound is used in the development of advanced materials, including polymers and nanomaterials, due to its ability to enhance material properties such as strength and thermal stability.
  • Medicinal Chemistry: Researchers utilize it in drug discovery processes, where it aids in the modification of drug candidates to improve their efficacy and selectivity.
  • Analytical Chemistry: It can be used as a standard in analytical methods, helping to improve the accuracy of measurements in various chemical analyses.

Citations