CAS 21205-91-4
:dimère de 9-BBN
- 9-Borabicyclo[3.3.1]nonane dimer
- Bis-9-borabicyclo[3.3.1]nonane
- 9-BBN Crystalline Dimer
9-BORABICYCLO[3.3.1]NONANE DIMER
CAS :Formule :C16H28B2Degré de pureté :95.0%Couleur et forme :SolidMasse moléculaire :242.029-BBN Dimer (Technical Grade)
CAS :Stability Moisture Sensitive, Hygroscopic
Applications 9-BBN dimer is a reagent that is used in the synthesis of 2,3,3a,12b-Tetradehydro Asenapine, which is a degredation product of Asenapine (A788000), a combined serotonin (5HT2) and dopamine (D2) receptor antagonist; structurally related to Mianserin. Antipsychotic.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Meltzer, H., et al.: J. Pharmacol. Exp. Ther., 251, 238 (1989); Schotte, A., et al.: Brain Res., 631, 191 (1993); Andree, B., et al.: Psychopharmacology, 131, 339 (1997); Richelson, E., et al.: Life Sci., 68, 29 (2000)Formule :C16H30B2Couleur et forme :NeatMasse moléculaire :244.039-BBN Dimer (Technical Grade)
CAS :9-BBN is a reactive borane that is used in organic synthesis as a reducing agent. It can be synthesized from diborane and methoxy groups. 9-BBN reacts with hydroxy groups to form α-pinene. The reaction mechanism of 9-BBN with amines has been studied using NMR spectroscopy and functional theory. The product of this reaction is the lactam, which has been shown to have reactive functional groups that can react with other molecules.
Formule :C16H30B2Degré de pureté :Min. 95%Masse moléculaire :244.03 g/mol9-BBN DIMER
CAS :Formule :C16H32B2Degré de pureté :96%Couleur et forme :SolidMasse moléculaire :244.0314






