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Catalog Number:
39934
CAS Number:
137297-49-5
(Bromometil)boronato de diisopropilo
Purity:
≥ 95% (GC)
Synonym(s):
Éster diisopropílico del ácido (bromometil)borónico
Hazmat
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$160.34 /1G
Tamaño
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Product Information

Diisopropyl (bromomethyl)boronate is a versatile organoboron compound recognized for its utility in organic synthesis and medicinal chemistry. This compound serves as a valuable reagent in the preparation of various boron-containing compounds, which are essential in the development of pharmaceuticals and agrochemicals. Its unique structure allows for selective functionalization, making it an ideal candidate for cross-coupling reactions, particularly in the formation of carbon-boron bonds. Researchers appreciate its ability to enhance reaction efficiency and improve yields, which is crucial in both academic and industrial settings.

In addition to its role in synthetic chemistry, diisopropyl (bromomethyl)boronate is increasingly utilized in the field of materials science, where it contributes to the development of advanced polymers and coatings. Its compatibility with various substrates and ease of handling make it a preferred choice for professionals seeking to innovate in material formulations. With its broad range of applications and significant advantages over similar compounds, diisopropyl (bromomethyl)boronate stands out as a key reagent for those looking to push the boundaries of chemical research and development.

Synonyms
Éster diisopropílico del ácido (bromometil)borónico
CAS Number
137297-49-5
Purity
≥ 95% (GC)
Molecular Formula
C7H16BBrO2
Molecular Weight
222.92
MDL Number
MFCD01631222
PubChem ID
2762526
Appearance
Líquido incoloro a ligeramente amarillo.
Refractive Index
n20D 1.43
Conditions
Conservar entre 2 y 8 °C.
General Information
Synonyms
Éster diisopropílico del ácido (bromometil)borónico
CAS Number
137297-49-5
Purity
≥ 95% (GC)
Molecular Formula
C7H16BBrO2
Molecular Weight
222.92
MDL Number
MFCD01631222
PubChem ID
2762526
Appearance
Líquido incoloro a ligeramente amarillo.
Refractive Index
n20D 1.43
Conditions
Conservar entre 2 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Diisopropyl (bromomethyl)boronate is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile reagent in the synthesis of various organic molecules, particularly in the formation of carbon-boron bonds, which are crucial for building complex structures in pharmaceuticals and agrochemicals.
  • Medicinal Chemistry: It plays a significant role in drug development, allowing researchers to create boron-containing compounds that can enhance the efficacy of therapeutic agents, particularly in cancer treatment.
  • Material Science: The compound is used in the development of advanced materials, including polymers and coatings, where its unique properties can improve durability and performance.
  • Cross-Coupling Reactions: It is employed in cross-coupling reactions, which are essential for forming carbon-carbon bonds, thus facilitating the creation of complex organic molecules in a more efficient manner compared to traditional methods.
  • Research and Development: This chemical is valuable in academic and industrial research settings for exploring new synthetic pathways and improving existing methodologies, making it a preferred choice for researchers looking to innovate.

Citas