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1,5-Diazabicyclo[4.3.0]non-5-ene_Molecular_structure_CAS_3001-72-7)
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1,5-Diazabicyclo[4.3.0]non-5-ene

Catalog No. A13437 Name Alfa Aesar
CAS Number 3001-72-7 Website
M. F. C7H12N2 Telephone
M. W. 124.18358 Fax
Purity 98% Email
Storage Chembase ID: 89784

SYNONYMS

Title
1,5-二氮双环[4.3.0]壬-5-烯
IUPAC name
2H,3H,4H,6H,7H,8H-pyrrolo[1,2-a]pyrimidine
IUPAC Traditional name
DBN
Synonyms
DBN

DATABASE IDS

CAS Number 3001-72-7
Beilstein Number 2417
EC Number 221-087-3
MDL Number MFCD00005554

PROPERTIES

Purity 98%
Boiling Point 95-98°C/7mm
Density 1.042
Flash Point 94°C(201°F)
Refractive Index 1.5200
GHS Pictograms GHS05
GHS Hazard statements H314-H318
European Hazard Symbols Corrosive Corrosive (C)
GHS Precautionary statements P260-P303+P361+P353-P305+P351+P338-P301+P330+P331-P405-P501A
Risk Statements 34
Safety Statements 26-36/37/39-45
Storage Warning Air Sensitive & Hygroscopic
TSCA Listed
Hazard Class 8
UN Number UN3267
Packing Group II

DETAILS

REFERENCES

  • The bicyclic amidines, DBN and DBU are strong organic bases initially introduced as reagents for dehydrohalogenation in vitamin A synthesis: Chem. Ber., 99, 2012 (1966).
  • For use of DBN in the aldol condensation, see: J. Am. Chem. Soc., 90, 3245 (1968). For esterification of thermally unstable carboxylic acids with diethyl sulfate at ambient temperature, see: Synth. Commun., 6, 89 (1976). For use in the alkylation of thiols with dihalomethanes, see: Synthesis, 952 (1980). In refluxing xylene, DBN and DBU cleave hindered esters, e.g. mesitoates, by alkyl-oxygen cleavage: Tetrahedron Lett., 3987 (1972); J. Org. Chem., 38, 1223 (1973).