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Catalog Number:
39885
CAS Number:
653589-95-8
2-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)benzoate de méthyle
Purity:
≥ 98% (CG)
Synonym(s):
2-(2-méthoxycarbonylphényl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane, Ester méthylique de l'acide 2-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)benzoïque, Ester pinacol de l'acide 2-(méthoxycarbonyl)phénylboronique
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Product Information

Methyl 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This compound features a unique dioxaborolane moiety, which enhances its reactivity and selectivity in various chemical reactions, making it an excellent choice for researchers and industry professionals focused on developing new materials and pharmaceuticals. Its structure allows for efficient coupling reactions, particularly in the formation of carbon-carbon bonds, which is crucial in the synthesis of complex organic molecules.

In practical applications, Methyl 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate has been employed in the synthesis of biologically active compounds, including pharmaceuticals and agrochemicals. Its stability and ease of use in laboratory settings make it a preferred reagent for chemists looking to streamline their synthesis processes. Additionally, the compound's unique properties offer advantages over similar boron-containing compounds, such as improved solubility and reactivity, which can lead to higher yields and more efficient reactions.

Synonyms
2-(2-méthoxycarbonylphényl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane, Ester méthylique de l'acide 2-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)benzoïque, Ester pinacol de l'acide 2-(méthoxycarbonyl)phénylboronique
CAS Number
653589-95-8
Purity
≥ 98% (CG)
Molecular Formula
C 14 H 19 BO 4
Molecular Weight
262.11
MDL Number
MFCD05663866
PubChem ID
2760076
Melting Point
43 - 47 ?C
Conditions
Magasin chez RT
General Information
Synonyms
2-(2-méthoxycarbonylphényl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane, Ester méthylique de l'acide 2-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)benzoïque, Ester pinacol de l'acide 2-(méthoxycarbonyl)phénylboronique
CAS Number
653589-95-8
Purity
≥ 98% (CG)
Molecular Formula
C 14 H 19 BO 4
Molecular Weight
262.11
MDL Number
MFCD05663866
PubChem ID
2760076
Melting Point
43 - 47 ?C
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

Methyl 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in organic chemistry, facilitating the creation of complex molecules through various coupling reactions.
  • Drug Development: It plays a crucial role in medicinal chemistry, where it can be used to modify drug candidates, enhancing their efficacy and bioavailability.
  • Material Science: The compound is employed in the development of advanced materials, including polymers and coatings, due to its unique boron-containing structure that improves thermal and mechanical properties.
  • Fluorescent Probes: It is utilized in creating fluorescent probes for biological imaging, allowing researchers to visualize cellular processes with high specificity and sensitivity.
  • Environmental Applications: The compound can be used in the synthesis of environmentally friendly pesticides and herbicides, providing effective solutions while minimizing ecological impact.

Citations