9-Borabicyclo[3.3.1]nonane - 0.4 M in hexanes

CAS : 280-64-8

Ref. 3D-FB158973

Informations sur le produit

• Nom: 9-Borabicyclo[3.3.1]nonane - 0.4 M in hexanes
• Synonymes: 9-Bbn, 9-Borabicyclo[3.3.1]Non-9-Yl, 9-Borabicyclononane, 9-Borylbicyclo[3.3.1]nonane, 9-borabicyclo(3.3.1)nonane, 9-Borabicyclo[3.3.1]nonane

Description

Borabicyclo[3.3.1]nonane is a functional group that has been used in the synthesis of α-pinene and other terpenoids. Borabicyclo[3.3.1]nonane can be synthesized by reacting α-pinene with methoxy groups and amines at high temperatures in the presence of a catalyst, such as boron trifluoride etherate. The reaction mechanism involves an elimination reaction followed by an addition reaction to form a lactam ring, which is then hydrolyzed to release 9-borabicyclo[3.3.1]nonane. This functional group has been used for the synthesis of α-pinene, which is a monoterpene found in pine needles and oil from turpentine trees, among other sources. The structural analysis shows that these molecules are linear chains with reactive sp2 hybridized carbons and hydroxyl groups on one end and alk

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 122.02 g/mol
• Formule: C₈H₁₅B
• Degré de pureté: Min. 95%
• InChI: InChI=1S/C8H15B/c1-3-7-5-2-6-8(4-1)9-7/h7-9H,1-6H2
• Code InChI: InChIKey=FEJUGLKDZJDVFY-UHFFFAOYSA-N
• SMILES: B1C2CCCC1CCC2