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Catalog Number:
39960
CAS Number:
365564-07-4
2-(3,5-diméthoxyphényl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane
Purity:
≥ 98% (CG)
Synonym(s):
Ester pinacol de l'acide 3,5-diméthoxyphénylboronique, 1,3-diméthoxy-5-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)benzène
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Product Information

2-(3,5-Dimethoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile boron-containing compound that has garnered attention in various fields, particularly in organic synthesis and medicinal chemistry. This compound is recognized for its unique structural features, which enhance its reactivity and selectivity in chemical reactions. Its ability to act as a boron source makes it invaluable in the development of boron-containing pharmaceuticals and agrochemicals. Researchers have utilized this compound in the synthesis of complex organic molecules, including those with potential therapeutic applications, showcasing its significance in drug discovery and development.

Moreover, the presence of dimethoxyphenyl groups contributes to its stability and solubility in organic solvents, making it an excellent candidate for various synthetic pathways. Its application extends to the field of materials science, where it can be used in the preparation of advanced materials with tailored properties. The compound's unique characteristics, such as its high reactivity and compatibility with diverse functional groups, position it as a preferred choice for researchers and industry professionals seeking efficient and effective solutions in their chemical processes.

Synonyms
Ester pinacol de l'acide 3,5-diméthoxyphénylboronique, 1,3-diméthoxy-5-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)benzène
CAS Number
365564-07-4
Purity
≥ 98% (CG)
Molecular Formula
C 14 H 21 BO 4
Molecular Weight
264.13
MDL Number
MFCD05865191
PubChem ID
16217660
Melting Point
88 - 92 ?C
Density
1,05 g/mL
Appearance
Poudre cristalline blanche à blanc cassé
Boiling Point
374,47 °C (lit.)
Refractive Index
n20D = 1,49
Conditions
Magasin chez RT
General Information
Synonyms
Ester pinacol de l'acide 3,5-diméthoxyphénylboronique, 1,3-diméthoxy-5-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)benzène
CAS Number
365564-07-4
Purity
≥ 98% (CG)
Molecular Formula
C 14 H 21 BO 4
Molecular Weight
264.13
MDL Number
MFCD05865191
PubChem ID
16217660
Melting Point
88 - 92 ?C
Density
1,05 g/mL
Appearance
Poudre cristalline blanche à blanc cassé
Boiling Point
374,47 °C (lit.)
Refractive Index
n20D = 1,49
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

2-(3,5-Dimethoxyphenyl)-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 synthesis, particularly in the formation of carbon-boron bonds, which are crucial for creating complex organic molecules.
  • Medicinal Chemistry: It is employed in the development of pharmaceutical compounds, aiding in the design of new drugs that target specific biological pathways, enhancing therapeutic efficacy.
  • Material Science: The compound is used in the production of advanced materials, including polymers and coatings, which benefit from its unique chemical properties that improve durability and performance.
  • Fluorescent Probes: It acts as a building block for fluorescent probes in biological imaging, allowing researchers to visualize cellular processes with high specificity and sensitivity.
  • Environmental Chemistry: This chemical plays a role in the development of sensors for detecting environmental pollutants, contributing to efforts in monitoring and improving environmental health.

Citations