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Catalog Number:
39982
CAS Number:
443776-76-9
Alcool 3-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)benzylique
Purity:
≥ 98% (CG)
Synonym(s):
2-[3-(hydroxyméthyl)phényl]-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane, Ester pinacol de l'acide 3-(hydroxyméthyl)phénylboronique
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Product Information

3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl alcohol is a versatile compound known for its unique boron-containing structure, which enhances its reactivity and stability in various applications. This compound is particularly valuable in organic synthesis, serving as a key intermediate in the development of pharmaceuticals and agrochemicals. Its ability to participate in cross-coupling reactions makes it an essential building block for creating complex molecular architectures. Researchers appreciate its role in the synthesis of biologically active compounds, where it can facilitate the introduction of functional groups with precision.

Additionally, the compound's stability under various conditions allows for its use in diverse environments, making it suitable for both laboratory and industrial applications. Its unique properties enable chemists to explore innovative pathways in synthetic chemistry, potentially leading to the discovery of new therapeutic agents. With its practical applications and benefits, 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl alcohol stands out as a valuable resource for professionals seeking to enhance their research and development efforts.

Synonyms
2-[3-(hydroxyméthyl)phényl]-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane, Ester pinacol de l'acide 3-(hydroxyméthyl)phénylboronique
CAS Number
443776-76-9
Purity
≥ 98% (CG)
Molecular Formula
C 13 H 19 BO 3
Molecular Weight
234.1
MDL Number
MFCD09266196
PubChem ID
44118236
Melting Point
44 - 48 ?C
Appearance
Poudre blanche à blanc cassé en grumeaux
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
2-[3-(hydroxyméthyl)phényl]-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane, Ester pinacol de l'acide 3-(hydroxyméthyl)phénylboronique
CAS Number
443776-76-9
Purity
≥ 98% (CG)
Molecular Formula
C 13 H 19 BO 3
Molecular Weight
234.1
MDL Number
MFCD09266196
PubChem ID
44118236
Melting Point
44 - 48 ?C
Appearance
Poudre blanche à blanc cassé en grumeaux
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl alcohol is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in organic chemistry, facilitating the synthesis of various complex molecules, including pharmaceuticals and agrochemicals.
  • Drug Development: Its unique boron-containing structure enhances the solubility and bioavailability of drug candidates, making it valuable in the pharmaceutical industry for developing more effective medications.
  • Materials Science: The compound is used in the creation of advanced materials, such as polymers and coatings, that require specific properties like durability and resistance to environmental factors.
  • Bioconjugation: Researchers employ this chemical in bioconjugation processes, linking biomolecules to create targeted drug delivery systems, which improve the efficacy of treatments.
  • Fluorescent Probes: Its properties allow it to be used in the development of fluorescent probes for imaging applications in biological research, aiding in the visualization of cellular processes.

Citations