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Catalog Number:
40043
CAS Number:
325142-84-5
2-(3-Methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Purity:
≥ 98% (GC)
Synonym(s):
3-Methoxyphenylboronic acid pinacol ester, 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)anisole
Documents
$19.13 /1G
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Product Information

2-(3-Methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile boron-containing compound known for its unique properties and applications in organic synthesis and medicinal chemistry. This compound serves as an effective reagent in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Its ability to facilitate the synthesis of complex organic molecules makes it invaluable in the development of pharmaceuticals, agrochemicals, and advanced materials. Researchers appreciate its stability and ease of handling, which enhance its usability in various laboratory settings.

Additionally, the presence of the methoxyphenyl group contributes to its reactivity and selectivity, allowing for tailored synthesis in the creation of biologically active compounds. This compound's unique structure not only aids in the efficient formation of desired products but also minimizes by-products, making it a more sustainable choice compared to similar reagents. Its application in the synthesis of novel compounds holds significant potential for innovation in drug discovery and material science.

Synonyms
3-Methoxyphenylboronic acid pinacol ester, 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)anisole
CAS Number
325142-84-5
Purity
≥ 98% (GC)
Molecular Formula
C13H19BO3
Molecular Weight
234.1
MDL Number
MFCD05863915
PubChem ID
11413643
Density
1.04 g/mL
Appearance
Clear colorless liquid
Boiling Point
329 °C (Lit.)
Refractive Index
n20D = 1.50
Conditions
Store at 2 - 8 °C
General Information
Synonyms
3-Methoxyphenylboronic acid pinacol ester, 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)anisole
CAS Number
325142-84-5
Purity
≥ 98% (GC)
Molecular Formula
C13H19BO3
Molecular Weight
234.1
MDL Number
MFCD05863915
PubChem ID
11413643
Density
1.04 g/mL
Appearance
Clear colorless liquid
Boiling Point
329 °C (Lit.)
Refractive Index
n20D = 1.50
Conditions
Store at 2 - 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-(3-Methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile reagent in organic chemistry, particularly in the synthesis of complex organic molecules, allowing for efficient carbon-carbon bond formation.
  • Medicinal Chemistry: It is employed in the development of pharmaceutical compounds, aiding in the creation of new drugs with improved efficacy and reduced side effects.
  • Material Science: The compound is used in the formulation of advanced materials, including polymers and coatings, enhancing their properties such as durability and resistance to environmental factors.
  • Bioconjugation: It plays a crucial role in bioconjugation techniques, which are essential for labeling biomolecules, facilitating studies in biochemistry and molecular biology.
  • Environmental Applications: The compound is also explored for its potential in environmental chemistry, particularly in the development of sensors for detecting pollutants, contributing to environmental monitoring efforts.

Citations