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Catalog Number:
40024
CAS Number:
72824-04-5
2-Allyl-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane (stabilisé avec de la phénothiazine)
Purity:
≥ 96,5 % (CG)
Synonym(s):
Ester pinacol d'acide allylboronique (stabilisé avec de la phénothiazine)
Hazmat
Documents
$40.96 /1G
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Product Information

2-Allyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, stabilized with Phenothiazine, is a versatile compound widely utilized in organic synthesis and materials science. This dioxaborolane derivative is particularly valued for its ability to serve as a boron source in various chemical reactions, including cross-coupling reactions and the formation of boron-containing polymers. Its unique structure enhances stability and reactivity, making it an excellent choice for researchers looking to develop novel materials or optimize synthetic pathways. The incorporation of Phenothiazine not only stabilizes the compound but also enhances its performance in light-sensitive applications, making it suitable for photochemical processes.

In the pharmaceutical industry, 2-Allyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane can be employed in the synthesis of complex organic molecules, facilitating the development of new drugs and therapeutic agents. Its ability to participate in selective reactions allows for greater control over product formation, which is crucial in medicinal chemistry. Additionally, this compound's compatibility with various reaction conditions makes it an attractive option for both academic research and industrial applications, providing a reliable tool for chemists aiming to innovate and streamline their processes.

Synonyms
Ester pinacol d'acide allylboronique (stabilisé avec de la phénothiazine)
CAS Number
72824-04-5
Purity
≥ 96,5 % (CG)
Molecular Formula
C 9 H 17 BO 2
Molecular Weight
0
MDL Number
MFCD00013347
PubChem ID
2763171
Density
0,89 g/mL
Appearance
Liquide clair et incolore
Boiling Point
35 °C / 1 mmHg (Lit.)
Refractive Index
n20D = 1,43
Conditions
Conserver à ≤ -4 °C
General Information
Synonyms
Ester pinacol d'acide allylboronique (stabilisé avec de la phénothiazine)
CAS Number
72824-04-5
Purity
≥ 96,5 % (CG)
Molecular Formula
C 9 H 17 BO 2
Molecular Weight
0
MDL Number
MFCD00013347
PubChem ID
2763171
Density
0,89 g/mL
Appearance
Liquide clair et incolore
Boiling Point
35 °C / 1 mmHg (Lit.)
Refractive Index
n20D = 1,43
Conditions
Conserver à ≤ -4 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Oui
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

2-Allyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (stabilized with Phenothiazine) 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. Its unique structure allows for selective reactions, making it valuable for synthesizing complex molecules.
  • Polymer Chemistry: It is employed in the development of advanced polymers. The compound can act as a cross-linking agent, enhancing the mechanical properties and thermal stability of polymeric materials, which is crucial in industries like automotive and packaging.
  • Pharmaceutical Development: In drug formulation, it plays a role in creating boron-containing compounds that exhibit biological activity. This application is particularly relevant in the development of new therapeutics with improved efficacy and reduced side effects.
  • Materials Science: The chemical is used in the synthesis of functional materials, such as sensors and catalysts. Its ability to form stable complexes with metals makes it ideal for creating innovative materials with specific properties.
  • Environmental Applications: It can be utilized in the remediation of pollutants, acting as a reagent in processes that convert harmful substances into less toxic forms. This application is increasingly important in addressing environmental challenges.

Citations