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CAS 21205-91-4

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9-BBN dimer

Description:
9-BBN dimer, or 9-borabicyclo[3.3.1]nonane dimer, is a chemical compound that serves as a boron-based reagent in organic synthesis, particularly in hydroboration reactions. It is characterized by its bicyclic structure, which includes a boron atom integrated into a bicyclic framework, enhancing its reactivity. The compound is typically a colorless to pale yellow liquid and is known for its ability to selectively add across double bonds in alkenes, making it valuable in the formation of organoboron compounds. 9-BBN dimer is less toxic compared to other boron reagents, but it should still be handled with care due to its potential reactivity. It is soluble in common organic solvents, which facilitates its use in various synthetic applications. The dimerization of 9-BBN enhances its stability and reactivity, allowing for more controlled reactions in synthetic organic chemistry. Overall, 9-BBN dimer is a versatile reagent that plays a significant role in the functionalization of organic molecules.
Formula:C16H30B2
InChI:InChI=1/2C8H15B/c2*1-3-7-5-2-6-8(4-1)9-7/h2*7-9H,1-6H2
SMILES:C1CC2CCCC(C1)B2.C1CC2CCCC(C1)B2
Synonyms:
  • 9-Borabicyclo[3.3.1]nonane dimer
  • Bis-9-borabicyclo[3.3.1]nonane
  • 9-BBN Crystalline Dimer
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