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Catalog Number:
31473
CAS Number:
1201905-61-4
Éster de pinacol del ácido trans -2-etoxietenil-1-borónico
Purity:
≥ 95 % (HPLC)
Synonym(s):
(E)-2-(2-Etoxivinil)-4,4,5,5-tetrametil-1,3,2-dioxaborolano, Éster de pinacol del ácido (E)-2-etoxivinilborónico, Éster de pinacol del ácido E-2-etoxietenil-1-borónico, Éster de pinacol del ácido (E)-1-etoxietano-2-borónico
Hazmat
Documents
$58.39 /1G
Tamaño
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Product Information

trans-2-Ethoxyethenyl-1-boronic acid pinacol ester is a versatile boronic acid derivative that plays a crucial role in organic synthesis and medicinal chemistry. This compound is particularly valued for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the formation of carbon-carbon bonds. Its unique structure enhances its reactivity and selectivity, allowing researchers to create complex molecules with precision. Additionally, the presence of the ethoxy group provides increased solubility in organic solvents, facilitating its use in various synthetic pathways.

In the pharmaceutical industry, trans-2-Ethoxyethenyl-1-boronic acid pinacol ester is utilized in the development of novel therapeutic agents, particularly in the synthesis of biologically active compounds. Its application extends to materials science, where it can be employed in the design of advanced polymers and functional materials. With its favorable properties and broad applicability, this compound is an invaluable resource for researchers and industry professionals seeking to innovate and enhance their chemical processes.

Synonyms
(E)-2-(2-Etoxivinil)-4,4,5,5-tetrametil-1,3,2-dioxaborolano, Éster de pinacol del ácido (E)-2-etoxivinilborónico, Éster de pinacol del ácido E-2-etoxietenil-1-borónico, Éster de pinacol del ácido (E)-1-etoxietano-2-borónico
CAS Number
1201905-61-4
Purity
≥ 95 % (HPLC)
Molecular Formula
C 10 H 19 BO 3
Molecular Weight
198.07
MDL Number
MFCD09998813
PubChem ID
53395424
Density
0,935 g/ml a 25 °C
Appearance
Líquido amarillo claro
Boiling Point
50 ?C
Refractive Index
número 20/D 1.447
Conditions
Conservar entre 2 y 8°C.
General Information
Synonyms
(E)-2-(2-Etoxivinil)-4,4,5,5-tetrametil-1,3,2-dioxaborolano, Éster de pinacol del ácido (E)-2-etoxivinilborónico, Éster de pinacol del ácido E-2-etoxietenil-1-borónico, Éster de pinacol del ácido (E)-1-etoxietano-2-borónico
CAS Number
1201905-61-4
Purity
≥ 95 % (HPLC)
Molecular Formula
C 10 H 19 BO 3
Molecular Weight
198.07
MDL Number
MFCD09998813
PubChem ID
53395424
Density
0,935 g/ml a 25 °C
Appearance
Líquido amarillo claro
Boiling Point
50 ?C
Refractive Index
número 20/D 1.447
Conditions
Conservar entre 2 y 8°C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

trans-2-Ethoxyethenyl-1-boronic acid pinacol ester is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Chemical Reactions: It is employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, which allows for the formation of carbon-carbon bonds, crucial for creating diverse chemical structures.
  • Material Science: The compound is used in the development of advanced materials, including polymers and nanomaterials, enhancing properties like strength and stability.
  • Drug Development: In medicinal chemistry, it aids in the design of new drug candidates by modifying existing compounds to improve efficacy and reduce side effects.
  • Analytical Chemistry: It can be utilized as a reagent in analytical methods, helping to detect and quantify specific compounds in various samples.

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