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Catalog Number:
39953
CAS Number:
210907-84-9
3-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)aniline
Purity:
≥ 98 % (RMN)
Synonym(s):
Ester pinacolique de l'acide 3-aminophénylboronique, 2-(3-aminophényl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane
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Product Information

3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline is a versatile compound known for its unique boron-containing structure, which enhances its utility in various applications. This compound is particularly valuable in organic synthesis and materials science, where it serves as a key intermediate in the development of pharmaceuticals and agrochemicals. Its dioxaborolane moiety contributes to its stability and reactivity, making it an excellent candidate for cross-coupling reactions, such as Suzuki-Miyaura coupling, which are pivotal in forming carbon-carbon bonds.

Researchers and industry professionals can leverage this compound for the synthesis of complex organic molecules, including biologically active compounds and functional materials. Its ability to facilitate efficient reactions while maintaining high selectivity makes it a preferred choice in laboratories focused on drug discovery and development. Additionally, the compound's unique properties may lead to innovations in polymer chemistry and nanotechnology, providing exciting opportunities for advancements in these fields.

Synonyms
Ester pinacolique de l'acide 3-aminophénylboronique, 2-(3-aminophényl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane
CAS Number
210907-84-9
Purity
≥ 98 % (RMN)
Molecular Formula
C 12 H 18 BNO 2
Molecular Weight
219.09
MDL Number
MFCD03453668
PubChem ID
2734655
Melting Point
93 - 95 ?C
Appearance
Blanc cassé uni
Conditions
Magasin chez RT
General Information
Synonyms
Ester pinacolique de l'acide 3-aminophénylboronique, 2-(3-aminophényl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane
CAS Number
210907-84-9
Purity
≥ 98 % (RMN)
Molecular Formula
C 12 H 18 BNO 2
Molecular Weight
219.09
MDL Number
MFCD03453668
PubChem ID
2734655
Melting Point
93 - 95 ?C
Appearance
Blanc cassé uni
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

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

  • Organic Synthesis: This compound serves as a versatile building block in organic chemistry, enabling the synthesis of complex molecules through its unique boron-containing structure.
  • Medicinal Chemistry: It plays a crucial role in the development of pharmaceutical compounds, particularly in the design of targeted therapies due to its ability to form stable bonds with various biological targets.
  • Materials Science: The compound is used in the creation of advanced materials, such as polymers and coatings, which benefit from its chemical stability and functional properties.
  • Fluorescent Probes: It can be employed in the development of fluorescent probes for biological imaging, allowing researchers to visualize cellular processes with high specificity.
  • Environmental Applications: The compound is explored for its potential in environmental chemistry, particularly in the detection and remediation of pollutants due to its reactive nature.

Citations