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Catalog Number:
39941
CAS Number:
454185-98-9
2-[4-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)phényl]acétate de méthyle
Purity:
≥ 98% (CG)
Synonym(s):
Ester pinacol de l'acide 4-(méthoxycarbonylméthyl)phénylboronique, 2-[(4-méthoxycarbonylméthyl)phényl]-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane, Ester méthylique de l'acide 2-[4-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)phényl]acétique
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Product Information

Methyl 2-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acetate is a versatile compound with significant applications in organic synthesis and materials science. This compound features a unique boron-containing structure, which enhances its reactivity and makes it an excellent candidate for cross-coupling reactions, particularly in the development of pharmaceuticals and agrochemicals. Its ability to participate in Suzuki-Miyaura coupling reactions allows researchers to create complex molecular architectures efficiently, making it invaluable in the synthesis of biologically active compounds.

Additionally, Methyl 2-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acetate is recognized for its stability and ease of handling, which are critical for industrial applications. This compound can be utilized in the production of advanced materials, including polymers and coatings, where its unique properties can enhance performance characteristics. With its broad range of applications and benefits, this compound is an essential tool for researchers and industry professionals looking to innovate and improve their product offerings.

Synonyms
Ester pinacol de l'acide 4-(méthoxycarbonylméthyl)phénylboronique, 2-[(4-méthoxycarbonylméthyl)phényl]-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane, Ester méthylique de l'acide 2-[4-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)phényl]acétique
CAS Number
454185-98-9
Purity
≥ 98% (CG)
Molecular Formula
C 15 H 21 BO 4
Molecular Weight
276.14
MDL Number
MFCD09997797
PubChem ID
11219601
Melting Point
49 - 53 ?C
Appearance
Poudre cristalline blanche à orange
Conditions
Magasin chez RT
General Information
Synonyms
Ester pinacol de l'acide 4-(méthoxycarbonylméthyl)phénylboronique, 2-[(4-méthoxycarbonylméthyl)phényl]-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane, Ester méthylique de l'acide 2-[4-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)phényl]acétique
CAS Number
454185-98-9
Purity
≥ 98% (CG)
Molecular Formula
C 15 H 21 BO 4
Molecular Weight
276.14
MDL Number
MFCD09997797
PubChem ID
11219601
Melting Point
49 - 53 ?C
Appearance
Poudre cristalline blanche à orange
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Methyl 2-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acetate is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in organic chemistry, enabling the creation of complex molecules for pharmaceuticals and agrochemicals.
  • Drug Development: Its unique boron-containing structure enhances the efficacy of drug candidates, particularly in targeting specific biological pathways, making it valuable in medicinal chemistry.
  • Material Science: Used in the synthesis of advanced materials, it contributes to the development of polymers with improved mechanical properties and thermal stability.
  • Fluorescent Probes: The compound can be utilized in creating fluorescent probes for biological imaging, aiding researchers in visualizing cellular processes in real-time.
  • Environmental Applications: Its properties allow for the design of compounds that can capture and degrade pollutants, thus playing a role in environmental remediation efforts.

Citations