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Catalog Number:
40060
CAS Number:
76347-13-2
2-Isopropyl-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane
Purity:
≥ 95% (CG)
Synonym(s):
Ester pinacolique d'acide isopropylboronique
Hazmat
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$131.90 /1G
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Product Information

2-Isopropyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile boron-containing compound known for its unique structural properties and reactivity. This compound is particularly valuable in organic synthesis, serving as a key intermediate in the preparation of various boron-based reagents. Its stability and ease of handling make it an excellent choice for researchers and industry professionals engaged in the development of pharmaceuticals, agrochemicals, and advanced materials. The presence of the dioxaborolane moiety enhances its utility in cross-coupling reactions, which are essential for constructing complex organic molecules.

Moreover, this compound's unique steric and electronic properties allow for selective functionalization, making it a preferred choice in synthetic chemistry. Its application extends to catalysis, where it can facilitate reactions under mild conditions, thus improving efficiency and yield. With its robust performance and adaptability, 2-Isopropyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane stands out as a valuable tool for chemists looking to innovate and streamline their synthetic processes.

Synonyms
Ester pinacolique d'acide isopropylboronique
CAS Number
76347-13-2
Purity
≥ 95% (CG)
Molecular Formula
C 9 H 19 BO 2
Molecular Weight
0
MDL Number
MFCD05663856
PubChem ID
12727711
Density
0,87 g/mL
Appearance
Liquide clair et incolore
Boiling Point
115 °C / 60 mm (lit.)
Refractive Index
n20D 1.41
Conditions
Magasin chez RT
General Information
Synonyms
Ester pinacolique d'acide isopropylboronique
CAS Number
76347-13-2
Purity
≥ 95% (CG)
Molecular Formula
C 9 H 19 BO 2
Molecular Weight
0
MDL Number
MFCD05663856
PubChem ID
12727711
Density
0,87 g/mL
Appearance
Liquide clair et incolore
Boiling Point
115 °C / 60 mm (lit.)
Refractive Index
n20D 1.41
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

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

  • Organic Synthesis: This compound serves as a versatile boron reagent in organic chemistry, facilitating the formation of carbon-boron bonds. Its unique structure allows for efficient coupling reactions, making it valuable in synthesizing complex organic molecules.
  • Pharmaceutical Development: In the pharmaceutical industry, it is used to create boron-containing compounds that can enhance drug efficacy. Its ability to stabilize reactive intermediates can lead to more effective therapeutic agents.
  • Material Science: The compound is applied in developing advanced materials, particularly in creating polymers with enhanced properties. Its incorporation can improve thermal stability and mechanical strength in various applications.
  • Agricultural Chemistry: It is utilized in agrochemical formulations to improve the delivery and effectiveness of pesticides and herbicides. The compound can enhance the solubility and bioavailability of active ingredients, leading to better crop protection.
  • Analytical Chemistry: This chemical is employed in analytical methods for detecting and quantifying various substances. Its unique properties make it suitable for use in chromatography and mass spectrometry, aiding in precise measurements.

Citations