![1,5-diazabicyclo[4.3.0]non-5-ene](https://commons.wikimedia.org/wiki/Special:FilePath/Synthesis-of-DBN.svg)
1,5-diazabicyclo[4.3.0]non-5-ene
Also known as DBN
1,5-Diazabicyclo[4.3.0]non-5-ene (DBN) is a chemical compound with the formula CHN. It is an amidine base used in organic synthesis. A related compound with related functions is [[DBU (chemistry)|1,8-diazabicyclo[5.4.0]undec-7-ene]] (DBU). The relatively complex nature of the formal names for DBU and DBN (hence the common use of acronyms) reflects the fact that these compounds are bicyclic and contain several functional groups.
Wikidata facts
- Mass
- 124.1
Show 6 more facts
- canonical SMILES
- C1CC2=NCCCN2C1
- chemical formula
- C₇H₁₂N₂
- boiling point
- 96
- density
- 1.005
- refractive index
- 1.5190
- Commons category
- 1,5-Diazabicyclo(4.3.0)non-5-ene (DBN)
Sources (2)
via Wikidata · CC0
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Article
5 sectionsContents
- Synthesis
- Uses
- As a base in organic synthesis
- DBN salt as an ionic liquid
- References
1,5-Diazabicyclo[4.3.0]non-5-ene (DBN) is a chemical compound with the formula CHN. It is an amidine base used in organic synthesis. A related compound with related functions is [[DBU (chemistry)|1,8-diazabicyclo[5.4.0]undec-7-ene]] (DBU). The relatively complex nature of the formal names for DBU and DBN (hence the common use of acronyms) reflects the fact that these compounds are bicyclic and contain several functional groups.
==Synthesis== DBN could be synthesized in the following manner, similarly to DBU: frameless|alt=Synthesis of DBN|600px