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Catalog Number:
39979
CAS Number:
325142-93-6
2-(3,5-diméthylphényl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane
Purity:
≥ 97% (CG)
Synonym(s):
5-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)- m -xylène, Ester pinacol de l'acide 3,5-diméthylphénylboronique
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Product Information

2-(3,5-Dimethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile organoboron compound known for its unique structural properties and reactivity. This compound is particularly valuable in organic synthesis, serving as a key intermediate in the development of various pharmaceuticals and agrochemicals. Its ability to participate in cross-coupling reactions makes it an essential reagent for researchers looking to create complex molecular architectures. The presence of the dioxaborolane moiety enhances its stability and solubility, facilitating its use in diverse chemical environments.

In addition to its synthetic applications, this compound is also recognized for its potential in materials science, particularly in the development of advanced polymers and coatings. Its unique properties allow for modifications that can enhance the performance characteristics of materials, making it a sought-after choice for industry professionals. With its broad applicability and advantageous features, 2-(3,5-Dimethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane stands out as a valuable tool for innovation in both research and industrial settings.

Synonyms
5-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)- m -xylène, Ester pinacol de l'acide 3,5-diméthylphénylboronique
CAS Number
325142-93-6
Purity
≥ 97% (CG)
Molecular Formula
C 14 H 21 BO 2
Molecular Weight
232.13
MDL Number
MFCD10000955
PubChem ID
15906198
Melting Point
112 °C (lit.)
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Magasin chez RT
General Information
Synonyms
5-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)- m -xylène, Ester pinacol de l'acide 3,5-diméthylphénylboronique
CAS Number
325142-93-6
Purity
≥ 97% (CG)
Molecular Formula
C 14 H 21 BO 2
Molecular Weight
232.13
MDL Number
MFCD10000955
PubChem ID
15906198
Melting Point
112 °C (lit.)
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

2-(3,5-Dimethylphenyl)-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, particularly in the formation of carbon-carbon bonds, making it valuable for synthesizing complex organic molecules.
  • Pharmaceutical Development: It is used in the development of pharmaceutical intermediates, aiding in the creation of new drugs with improved efficacy and reduced side effects.
  • Material Science: The compound is applied in the production of advanced materials, including polymers and coatings, which benefit from its unique chemical properties.
  • Bioconjugation: It plays a role in bioconjugation techniques, allowing for the attachment of biomolecules to surfaces or other molecules, enhancing the functionality of biosensors and drug delivery systems.
  • Environmental Chemistry: This chemical is explored for its potential in environmental applications, such as the development of sensors for detecting pollutants, contributing to environmental monitoring efforts.

Citations