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Catalog Number:
31473
CAS Number:
1201905-61-4
trans-2-Ethoxyethenyl-1-boronic acid pinacol ester
Purity:
≥ 95% (HPLC)
Synonym(s):
(E)-2-(2-Ethoxyvinyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, (E)-2-Ethoxyvinylboronic acid pinacol ester, E-2-Ethoxyethenyl-1-boronic acid pinacol ester, (E)-1-Ethoxyethene-2-boronic acid pinacol ester
Hazmat
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$58.39 /1G
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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-Ethoxyvinyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, (E)-2-Ethoxyvinylboronic acid pinacol ester, E-2-Ethoxyethenyl-1-boronic acid pinacol ester, (E)-1-Ethoxyethene-2-boronic acid pinacol ester
CAS Number
1201905-61-4
Purity
≥ 95% (HPLC)
Molecular Formula
C10H19BO3
Molecular Weight
198.07
MDL Number
MFCD09998813
PubChem ID
53395424
Density
0.935 g/ml at 25 ?C
Appearance
Light yellow liquid
Boiling Point
50 ?C
Refractive Index
n20/D 1.447
Conditions
Store at 2 - 8°C
General Information
Synonyms
(E)-2-(2-Ethoxyvinyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, (E)-2-Ethoxyvinylboronic acid pinacol ester, E-2-Ethoxyethenyl-1-boronic acid pinacol ester, (E)-1-Ethoxyethene-2-boronic acid pinacol ester
CAS Number
1201905-61-4
Purity
≥ 95% (HPLC)
Molecular Formula
C10H19BO3
Molecular Weight
198.07
MDL Number
MFCD09998813
PubChem ID
53395424
Density
0.935 g/ml at 25 ?C
Appearance
Light yellow liquid
Boiling Point
50 ?C
Refractive Index
n20/D 1.447
Conditions
Store at 2 - 8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Yes
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.

Citations