CAS 3001-72-7
:1,5-Diazabicyclo[4.3.0]non-5-ene
Description:
1,5-Diazabicyclo[4.3.0]non-5-ene, commonly referred to as DBN, is a bicyclic organic compound characterized by its unique structure that includes two nitrogen atoms within a bicyclic framework. It is a colorless to pale yellow liquid at room temperature and is known for its strong basicity, making it a useful reagent in organic synthesis, particularly in deprotonation reactions. DBN is often employed as a catalyst or a base in various chemical transformations, including the synthesis of heterocycles and in polymerization processes. Its high basicity is attributed to the presence of the diazabicyclic structure, which stabilizes the conjugate acid formed during reactions. Additionally, DBN is relatively stable under standard conditions but can be sensitive to moisture and air, necessitating careful handling and storage. Its applications extend to the pharmaceutical and agrochemical industries, where it serves as a versatile building block in the synthesis of complex molecules. Overall, DBN is a valuable compound in the field of organic chemistry due to its reactivity and structural properties.
Formula:C7H12N2
InChI:InChI=1S/C7H12N2/c1-3-7-8-4-2-6-9(7)5-1/h1-6H2
InChI key:InChIKey=SGUVLZREKBPKCE-UHFFFAOYSA-N
SMILES:C1=2N(CCC1)CCCN2
Synonyms:- 1,5-Diazabicyclo[4.3.0]nonene-5
- 1,5-Diazobiciclo[4.3.0]Non-5-Eno
- 1,5-Diazobicyclo[4.3.0]Non-5-Ene
- 1,5-Diazobicyclo[4.3.0]non-5-en
- 2,3,4,6,7,8-Hexahydropyrrolo[1,2-a]pyrimidine
- 2H,3H,4H,6H,7H,8H-Pyrrolo[1,2-a]pyrimidine
- Bicyclo[4.3.0]Nona-5-Ene, 1,5-Diaza-
- D 1313
- DBN
- DBN (heterocycle)
- Diazabicyclononene
- Nsc 118106
- Pyrrolo[1,2-a]pyrimidine, 2,3,4,6,7,8-hexahydro-
- U-Cat 1102
- Ws-A 201
- See more synonyms
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Found 7 products.
1,5-Diazabicyclo[4.3.0]non-5-ene, 98%
CAS:<p>1,5-Diazabicyclo[4.3.0]non-5-ene is employed for dehydrohalogenation reactions and base-catalyzed rearrangements in organic synthesis. It is an amidine base used in organic synthesis. Further, it is used as a resin curing agent and polyurethane catalyst. This Thermo Scientific Chemicals brand pro</p>Formula:C7H12N2Purity:98%Color and Shape:Clear colorless to yellow, LiquidMolecular weight:124.192,3,4,6,7,8-Hexahydropyrrolo[1,2-a]pyrimidine
CAS:Formula:C7H12N2Purity:95%Color and Shape:LiquidMolecular weight:124.18361,5-Diazabicyclo[4.3.0]non-5-ene
CAS:<p>1,5-Diazabicyclo[4.3.0]non-5-ene</p>Formula:C7H12N2Purity:98%Color and Shape: clear. light yellow liquidMolecular weight:124.18358g/mol1,5-Diazabicyclo(4.3.0)non-5-ene
CAS:Formula:C7H12N2Purity:≥ 98.0%Color and Shape:Colourless to light yellow liquidMolecular weight:124.191,5-Diazabicyclo[4.3.0]non-5-ene
CAS:Formula:C7H12N2Purity:99.0%Color and Shape:Liquid, ClearMolecular weight:124.1871,5-Diazabicyclo[4.3.0]-5-nonene
CAS:Formula:C7H12N2Purity:>98.0%(GC)Color and Shape:Colorless to Light orange to Yellow clear liquidMolecular weight:124.191,5-Diazabicyclo[4.3.0]non-5-ene
CAS:Controlled Product<p>Applications 1,5-Diazabicyclo[4.3.0]non-5-ene is used as a nucleophilic catalyst for the Freidel-Crafts C-acylation of pyrroles and indoles. 1,5-Diazabicyclo[4.3.0]non-5-ene is also an inhibitor of indoleamine-N-methyltransferase (II) of rabbit lung in vitro.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Mandel, L.: Biochem. Pharmacol., 25, 2251 (1976); Taylor, J., et al.: Org. Lett., 12, 5740 (2010)<br></p>Formula:C7H12N2Color and Shape:NeatMolecular weight:124.18






