For research use only. Not for therapeutic Use.
1,5-Diazabicyclo[4.3.0]non-5-ene (Cat No.: R044528), commonly abbreviated as DBN, is a strong, non-nucleophilic organic base featuring a bicyclic amidine structure. It is widely used in organic synthesis for deprotonation, elimination, and condensation reactions due to its high basicity and steric hindrance. DBN is especially useful in base-catalyzed transformations where minimal nucleophilic interference is required. Its rigid structure and solubility in organic solvents make it an effective catalyst or reagent in both laboratory and industrial settings. For research and chemical synthesis use only.
CAS Number | 3001-72-7 |
Synonyms | 2,3,4,6,7,8-Hexahydropyrrolo[1,2-a]pyrimidine; ?1,5-Diazabicyclo[4.3.0]nonene-5; 2,3,4,6,7,8-Hexahydropyrrolo[1,2-a]pyrimidine; D 1313; DBN; DBN (heterocycle); NBU; NSC 11810 |
Molecular Formula | C7H12N2 |
Purity | ≥95% |
Storage | -20°C |
IUPAC Name | 2,3,4,6,7,8-hexahydropyrrolo[1,2-a]pyrimidine |
InChI | InChI=1S/C7H12N2/c1-3-7-8-4-2-6-9(7)5-1/h1-6H2 |
InChIKey | SGUVLZREKBPKCE-UHFFFAOYSA-N |
SMILES | C1CC2=NCCCN2C1 |
Chemistry Calculators | Dilution Calculator In vivo Formulation Calculator Molarity Calculator Molecular Weight Calculator Reconstitution Calculator |