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Catalog Number:
41436
CAS Number:
85116-37-6
(-)- B -Chlorodiisopinocampheylborane (60 % dans l'hexane, environ 1,7 mol/L)
Purity:
≥ 60 % (dosage par titration)
Hazmat
Documents
$368.95 /100ML
Taille
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Informations sur le produit

(-)-B-Chlorodiisopinocampheylborane is a highly specialized reagent known for its unique properties and applications in organic synthesis, particularly in asymmetric synthesis and organometallic chemistry. This compound, available in a 60% concentration in hexane, is valued for its ability to facilitate selective reactions, making it an essential tool for researchers and industry professionals engaged in the development of complex organic molecules. Its chiral nature allows for the creation of enantiomerically enriched products, which is crucial in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs) that require specific stereochemistry for efficacy.

The compound's effectiveness in various coupling reactions and its compatibility with a range of substrates make it a versatile choice for chemists looking to enhance reaction yields and selectivity. Its application extends to the synthesis of natural products and the development of novel materials, showcasing its importance in both academic research and industrial processes. With its unique properties, (-)-B-Chlorodiisopinocampheylborane stands out as a valuable reagent for advancing chemical research and innovation.

Numéro CAS 
85116-37-6
Formule moléculaire
C20H34BCl
Poids moléculaire 
0
Informations générales
Numéro CAS 
85116-37-6
Formule moléculaire
C20H34BCl
Poids moléculaire 
0
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:

  • Synthetic Chemistry: This compound serves as a crucial reagent in asymmetric synthesis, enabling chemists to create chiral molecules with high selectivity, which is essential in pharmaceuticals.
  • Organometallic Chemistry: It acts as a boron source in various reactions, facilitating the formation of carbon-boron bonds, which are important in the development of new materials and fine chemicals.
  • Drug Development: Researchers leverage its unique properties to enhance the efficacy of drug candidates, particularly in optimizing the stereochemistry of active pharmaceutical ingredients.
  • Material Science: This compound is utilized in the synthesis of advanced polymers and materials, providing enhanced properties such as improved thermal stability and mechanical strength.
  • Green Chemistry: Its use in reactions often leads to less waste and byproducts, aligning with sustainable practices in chemical manufacturing and research.

Citations