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Catalog Number:
23423
CAS Number:
1309981-67-6
Éster de pinacol del ácido 2-Boc-5-metoxifenilborónico
Purity:
≥ 98% (RMN)
Documents
$79.22 /100 mg
Tamaño
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Product Information

2-Boc-5-methoxyphenylboronic acid pinacol ester is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and reactivity, making it an ideal candidate for cross-coupling reactions and the formation of complex organic molecules. Its unique structure allows for the selective functionalization of aromatic compounds, facilitating the development of pharmaceuticals and agrochemicals. Researchers appreciate its role in Suzuki-Miyaura coupling, where it serves as a key building block for synthesizing biologically active compounds.

The compound's pinacol ester form offers additional advantages, including improved solubility and ease of handling in various solvents, which is crucial for laboratory applications. Its ability to participate in diverse chemical reactions positions it as a valuable tool for chemists aiming to innovate in drug discovery and material science. With its robust performance and adaptability, 2-Boc-5-methoxyphenylboronic acid pinacol ester stands out as a reliable choice for professionals seeking efficiency and effectiveness in their synthetic endeavors.

CAS Number
1309981-67-6
Purity
≥ 98% (RMN)
Molecular Formula
C 18 H 27 BO 5
Molecular Weight
334.21
MDL Number
MFCD10698497
PubChem ID
45925997
Appearance
Polvo de color blanco a blanquecino
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
1309981-67-6
Purity
≥ 98% (RMN)
Molecular Formula
C 18 H 27 BO 5
Molecular Weight
334.21
MDL Number
MFCD10698497
PubChem ID
45925997
Appearance
Polvo de color blanco a blanquecino
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-Boc-5-methoxyphenylboronic 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.
  • Medicinal Chemistry: It plays a crucial role in drug discovery, especially in the design of boron-containing compounds that can enhance the efficacy of therapeutic agents.
  • Material Science: The compound is used in the creation of advanced materials, including polymers and nanomaterials, due to its unique chemical properties that allow for functionalization.
  • Chemical Biology: It is employed in the study of biological systems, facilitating the development of probes and sensors that can detect specific biomolecules.
  • Cross-Coupling Reactions: This chemical is particularly effective in Suzuki-Miyaura coupling reactions, offering advantages in selectivity and yield compared to other boronic acids.

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