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Catalog Number:
41440
CAS Number:
112246-73-8
+)- B -Chlorodiisopinocampheylborane (58 % dans l'hexane, environ 1,6 mol/L)
Purity:
90 - 105 % (dosage par titrage)
Hazmat
Documents
$375.36 /100ML
Taille
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Informations sur le produit

(+)-B-Chlorodiisopinocampheylborane is a specialized organoboron compound that serves as a powerful reagent in organic synthesis, particularly in asymmetric synthesis and catalysis. This compound, available in a 58% concentration in hexane, is known for its ability to facilitate the formation of carbon-carbon bonds, making it invaluable in the synthesis of complex organic molecules. Its unique structure allows for high selectivity and efficiency in reactions, which is particularly beneficial for researchers and industry professionals engaged in the development of pharmaceuticals and fine chemicals.

The compound's application extends to the synthesis of chiral intermediates, where it plays a crucial role in producing compounds with specific stereochemistry. This is especially relevant in the pharmaceutical industry, where the chirality of a compound can significantly influence its biological activity. Additionally, (+)-B-Chlorodiisopinocampheylborane offers advantages over similar reagents due to its stability and ease of handling, making it a preferred choice for chemists looking to optimize their synthetic pathways.

Numéro CAS 
112246-73-8
Formule moléculaire
C20H34BCl
Poids moléculaire 
0
Rotation optique 
[α] 20 D = 47 - 54 ° (Calculé sur une solution d'hexane)
Informations générales
Numéro CAS 
112246-73-8
Formule moléculaire
C20H34BCl
Poids moléculaire 
0
Rotation optique 
[α] 20 D = 47 - 54 ° (Calculé sur une solution d'hexane)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
-
Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
-
Applications

(+)-B-Chlorodiisopinocampheylborane is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a powerful reagent in asymmetric synthesis, allowing chemists to create chiral molecules efficiently, which is crucial in pharmaceuticals.
  • Drug Development: Its unique properties enable researchers to develop new drugs with specific stereochemistry, enhancing the efficacy and safety profiles of therapeutic agents.
  • Material Science: The compound is used in the development of advanced materials, particularly in creating polymers with tailored properties for applications in electronics and coatings.
  • Catalysis: It acts as a catalyst in various chemical reactions, improving reaction rates and selectivity, which is essential in industrial processes and research labs.
  • Environmental Chemistry: This chemical can be employed in studies aimed at understanding and mitigating environmental pollutants, contributing to greener chemistry practices.

Citations