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Catalog Number:
39887
CAS Number:
126689-00-7
4,4,5,5-tétraméthyl-2-(2-méthyl-1-propényl)-1,3,2-dioxaborolane
Purity:
≥ 98% (CG)
Synonym(s):
Ester pinacol de l'acide (2-méthyl-1-propényl)boronique
Hazmat
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$127.79 /1G
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Product Information

4,4,5,5-Tetramethyl-2-(2-methyl-1-propenyl)-1,3,2-dioxaborolane is a versatile 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 reagent in the formation of carbon-carbon bonds, making it invaluable in the synthesis of complex organic molecules. Its structure allows for selective reactivity, which can be advantageous in developing pharmaceuticals and agrochemicals. Additionally, its application in polymer chemistry is noteworthy, where it serves as a building block for creating functionalized polymers with tailored properties.

Researchers and industry professionals can leverage 4,4,5,5-Tetramethyl-2-(2-methyl-1-propenyl)-1,3,2-dioxaborolane for its efficiency in cross-coupling reactions, which are essential in the production of fine chemicals and advanced materials. Its stability and ease of handling further enhance its appeal, providing a reliable option for those looking to streamline their synthetic processes. With its growing relevance in the development of innovative materials and pharmaceuticals, this compound stands out as a key player in modern chemical research.

Synonyms
Ester pinacol de l'acide (2-méthyl-1-propényl)boronique
CAS Number
126689-00-7
Purity
≥ 98% (CG)
Molecular Formula
C 10 H 19 BO 2
Molecular Weight
182.07
MDL Number
MFCD09842762
PubChem ID
15148447
Density
0,90 g/mL
Appearance
Liquide clair légèrement jaune à orange
Boiling Point
71 ?C / 19 mmHg (Lit.)
Refractive Index
n20D 1.44
Conditions
Magasin chez RT
General Information
Synonyms
Ester pinacol de l'acide (2-méthyl-1-propényl)boronique
CAS Number
126689-00-7
Purity
≥ 98% (CG)
Molecular Formula
C 10 H 19 BO 2
Molecular Weight
182.07
MDL Number
MFCD09842762
PubChem ID
15148447
Density
0,90 g/mL
Appearance
Liquide clair légèrement jaune à orange
Boiling Point
71 ?C / 19 mmHg (Lit.)
Refractive Index
n20D 1.44
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Oui
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

4,4,5,5-Tetramethyl-2-(2-methyl-1-propenyl)-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 formation of carbon-carbon bonds, which is essential for creating complex molecules in pharmaceuticals and agrochemicals.
  • Drug Development: Its unique properties make it valuable in the synthesis of biologically active compounds, aiding researchers in developing new medications with improved efficacy and reduced side effects.
  • Material Science: The compound is used in the production of advanced materials, including polymers and coatings, enhancing their durability and chemical resistance, which is crucial for various industrial applications.
  • Analytical Chemistry: It acts as a reagent in analytical methods, helping to detect and quantify specific compounds in complex mixtures, thereby supporting quality control in manufacturing processes.
  • Agricultural Chemistry: This chemical is applied in the formulation of agrochemicals, contributing to the development of effective pesticides and herbicides that are essential for sustainable agriculture.

Citations