Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
39883
CAS Number:
380151-86-0
3-(4,4,5,5-Tetrametil-1,3,2-dioxaborolan-2-il)benzaldehído
Purity:
≥ 98% (GC)
Synonym(s):
Éster de pinacol del ácido 3-formilfenilborónico, 2-(3-formilfenil)-4,4,5,5-tetrametil-1,3,2-dioxaborolano
Documents
$72.31 /5G
Tamaño
Request Bulk Quote
Product Information

3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This compound features a unique dioxaborolane moiety, which enhances its reactivity and stability, making it an excellent choice for researchers focusing on boron chemistry. Its structure allows for efficient incorporation into various synthetic pathways, particularly in the development of pharmaceuticals and agrochemicals. The compound has shown promise in applications such as cross-coupling reactions, which are pivotal in forming carbon-carbon bonds, thus facilitating the creation of complex organic molecules.

Moreover, the presence of the benzaldehyde functional group provides additional reactivity, allowing for further derivatization and functionalization. This characteristic is particularly beneficial for researchers looking to explore new chemical entities or optimize existing compounds. With its unique properties and practical applications, 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde stands out as a valuable tool for both academic and industrial chemists aiming to innovate in their respective fields.

Synonyms
Éster de pinacol del ácido 3-formilfenilborónico, 2-(3-formilfenil)-4,4,5,5-tetrametil-1,3,2-dioxaborolano
CAS Number
380151-86-0
Purity
≥ 98% (GC)
Molecular Formula
C 13 H 17 BO 3
Molecular Weight
232.09
MDL Number
MFCD05663827
PubChem ID
2760586
Melting Point
51 - 55 ?C
Appearance
Polvo cristalino de color blanco a amarillo claro.
Conditions
Tienda en RT
General Information
Synonyms
Éster de pinacol del ácido 3-formilfenilborónico, 2-(3-formilfenil)-4,4,5,5-tetrametil-1,3,2-dioxaborolano
CAS Number
380151-86-0
Purity
≥ 98% (GC)
Molecular Formula
C 13 H 17 BO 3
Molecular Weight
232.09
MDL Number
MFCD05663827
PubChem ID
2760586
Melting Point
51 - 55 ?C
Appearance
Polvo cristalino de color blanco a amarillo claro.
Conditions
Tienda en RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde 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.
  • Fluorescent Probes: It can be employed in the creation of fluorescent probes for biological imaging, aiding researchers in visualizing cellular processes in real-time.
  • Cross-Coupling Reactions: The compound is effective in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is crucial for forming carbon-carbon bonds in various organic compounds.
  • Material Science: It finds applications in the development of advanced materials, including polymers and nanomaterials, enhancing their properties for electronics and coatings.
  • Medicinal Chemistry: Researchers utilize it in the design of new drug candidates, leveraging its unique structure to improve efficacy and reduce side effects in therapeutic applications.

Citas