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Catalog Number:
39916
CAS Number:
128376-64-7
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde
Purity:
≥ 97% (GC)
Synonym(s):
4-Formylphenylboronic acid pinacol ester, 2-(4-Formylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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Product Information

4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde is a versatile compound widely utilized in organic synthesis and materials science. This compound features a unique dioxaborolane moiety, which enhances its reactivity and stability, making it an excellent choice for various applications. Researchers often leverage its properties in the development of novel pharmaceuticals, agrochemicals, and advanced materials. Its ability to participate in cross-coupling reactions allows for the efficient formation of carbon-carbon bonds, which is crucial in the synthesis of complex organic molecules.

In addition to its synthetic utility, this compound is also recognized for its role in the development of fluorescent materials and sensors, providing significant advantages in analytical chemistry and environmental monitoring. Its stability under various conditions makes it a reliable choice for both laboratory and industrial applications. With its unique structural features and practical applications, 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde stands out as a valuable tool for researchers and industry professionals seeking innovative solutions in chemical synthesis and material development.

Synonyms
4-Formylphenylboronic acid pinacol ester, 2-(4-Formylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS Number
128376-64-7
Purity
≥ 97% (GC)
Molecular Formula
C13H17BO3
Molecular Weight
232.09
MDL Number
MFCD04972375
PubChem ID
2769536
Melting Point
59 - 63 ?C
Appearance
White to light yellow crystalline powder
Conditions
Store at RT
General Information
Synonyms
4-Formylphenylboronic acid pinacol ester, 2-(4-Formylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS Number
128376-64-7
Purity
≥ 97% (GC)
Molecular Formula
C13H17BO3
Molecular Weight
232.09
MDL Number
MFCD04972375
PubChem ID
2769536
Melting Point
59 - 63 ?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

4-(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 organic chemistry, facilitating the synthesis of various complex molecules, including pharmaceuticals and agrochemicals.
  • Fluorescent Probes: Its unique structure allows it to be used in developing fluorescent probes for biological imaging, enhancing the visualization of cellular processes in research.
  • Catalysis: It plays a role in catalytic reactions, particularly in cross-coupling reactions, which are essential for creating new carbon-carbon bonds in organic compounds.
  • Material Science: The compound is valuable in the production of advanced materials, such as polymers and coatings, that require specific chemical properties for improved performance.
  • Medicinal Chemistry: Researchers utilize it in drug discovery processes, where its reactivity can lead to the development of new therapeutic agents with enhanced efficacy.

Citations