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Catalog Number:
39883
CAS Number:
380151-86-0
3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde
Purity:
≥ 98% (GC)
Synonym(s):
3-Formylphenylboronic acid pinacol ester, 2-(3-Formylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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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
3-Formylphenylboronic acid pinacol ester, 2-(3-Formylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS Number
380151-86-0
Purity
≥ 98% (GC)
Molecular Formula
C13H17BO3
Molecular Weight
232.09
MDL Number
MFCD05663827
PubChem ID
2760586
Melting Point
51 - 55 ?C
Appearance
White to light yellow crystalline powder
Conditions
Store at RT
General Information
Synonyms
3-Formylphenylboronic acid pinacol ester, 2-(3-Formylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS Number
380151-86-0
Purity
≥ 98% (GC)
Molecular Formula
C13H17BO3
Molecular Weight
232.09
MDL Number
MFCD05663827
PubChem ID
2760586
Melting Point
51 - 55 ?C
Appearance
White to light yellow crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
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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.

Citations