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Catalog Number:
39977
CAS Number:
87100-28-5
2-Benzyl-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane
Purity:
≥ 97% (CG)
Synonym(s):
Ester pinacolique de l'acide benzylboronique
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Product Information

2-Benzyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile organoboron compound that has gained attention in various fields, particularly in organic synthesis and medicinal chemistry. This compound is recognized for its unique boron-containing structure, which enhances its reactivity and stability, making it an ideal candidate for applications in cross-coupling reactions and as a reagent in the synthesis of complex organic molecules. Its ability to facilitate the formation of carbon-carbon bonds positions it as a valuable tool for researchers aiming to develop new pharmaceuticals and agrochemicals.

Moreover, the compound's distinctive properties allow it to serve as a protective group in synthetic pathways, providing chemists with greater control over reaction conditions and product outcomes. Its compatibility with a range of functional groups further broadens its applicability in diverse chemical processes. Researchers and industry professionals can leverage 2-Benzyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane to streamline their synthesis protocols, improve yields, and explore innovative pathways in their projects.

Synonyms
Ester pinacolique de l'acide benzylboronique
CAS Number
87100-28-5
Purity
≥ 97% (CG)
Molecular Formula
C 13 H 19 BO 2
Molecular Weight
218.1
MDL Number
MFCD05663841
PubChem ID
3864964
Density
0,99 g/mL
Appearance
Liquide clair légèrement jaune à orange
Boiling Point
65 °C / 0,2 mmHg (Lit.)
Refractive Index
n20D = 1,49
Conditions
Conserver à ≤ -10 °C
General Information
Synonyms
Ester pinacolique de l'acide benzylboronique
CAS Number
87100-28-5
Purity
≥ 97% (CG)
Molecular Formula
C 13 H 19 BO 2
Molecular Weight
218.1
MDL Number
MFCD05663841
PubChem ID
3864964
Density
0,99 g/mL
Appearance
Liquide clair légèrement jaune à orange
Boiling Point
65 °C / 0,2 mmHg (Lit.)
Refractive Index
n20D = 1,49
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

2-Benzyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile reagent in organic chemistry, facilitating the formation of carbon-carbon bonds, which is crucial for synthesizing complex molecules.
  • Drug Development: Its unique boron-containing structure makes it valuable in medicinal chemistry, particularly in the design and synthesis of new pharmaceuticals with enhanced efficacy.
  • Material Science: The compound is used in developing advanced materials, including polymers and coatings, due to its ability to modify material properties and improve durability.
  • Catalysis: It acts as a catalyst in various chemical reactions, offering advantages such as increased reaction rates and selectivity, which are essential in industrial processes.
  • Environmental Applications: Its properties allow for potential use in environmental chemistry, such as in the development of sensors for detecting pollutants or in remediation processes.

Citations