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Catalog Number:
39963
CAS Number:
380151-85-9
2-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)benzaldéhyde
Purity:
≥ 97% (CG)
Synonym(s):
Ester pinacol de l'acide 2-formylphénylboronique, 2-(2-formylphényl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane
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Product Information

2-(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 looking to develop new materials or pharmaceuticals. Its structure allows for efficient incorporation into various chemical reactions, particularly in the formation of carbon-carbon bonds, which is crucial in the synthesis of complex organic molecules.

In practical applications, 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde has been employed in the development of novel agrochemicals and pharmaceuticals, showcasing its potential in creating effective solutions in these industries. Its ability to act as a versatile building block in the synthesis of biologically active compounds makes it a valuable asset for researchers and industry professionals alike. With its unique properties and broad applicability, this compound stands out as an essential tool for advancing chemical research and development.

Synonyms
Ester pinacol de l'acide 2-formylphénylboronique, 2-(2-formylphényl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane
CAS Number
380151-85-9
Purity
≥ 97% (CG)
Molecular Formula
C 13 H 17 BO 3
Molecular Weight
232.09
MDL Number
MFCD07363841
PubChem ID
10977322
Density
1,06 g/mL
Appearance
Liquide incolore à légèrement jaune
Refractive Index
n20D = 1,51
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
Ester pinacol de l'acide 2-formylphénylboronique, 2-(2-formylphényl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane
CAS Number
380151-85-9
Purity
≥ 97% (CG)
Molecular Formula
C 13 H 17 BO 3
Molecular Weight
232.09
MDL Number
MFCD07363841
PubChem ID
10977322
Density
1,06 g/mL
Appearance
Liquide incolore à légèrement jaune
Refractive Index
n20D = 1,51
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

2-(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 synthesis, enabling the creation of complex molecules in pharmaceuticals and agrochemicals.
  • Fluorescent Probes: It is used to develop fluorescent probes for biological imaging, helping researchers visualize cellular processes in real-time.
  • Material Science: The compound finds applications in the development of advanced materials, such as polymers and coatings, due to its unique chemical properties.
  • Catalysis: It acts as a catalyst in various chemical reactions, improving reaction efficiency and selectivity, which is crucial in industrial processes.
  • Drug Development: In medicinal chemistry, it aids in the design of new drug candidates, particularly in targeting specific biological pathways.

Citations