| Weight | 139.202 g/mol |
|---|---|
| Formula | C7H13N3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
5807-14-7 (5807-14-7)
1,3,4,6,7,8-hexahydro-2H-pyrimido(1,2-a)pyrimidine · hppH cpd
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 1,3,4,6,7,8-hexahydro-2H-pyrimido(1,2-a)pyrimidine
- hppH cpd
-
SMILESC1CNC2=NCCCN2C1
-
InChIKeyFVKFHMNJTHKMRX-UHFFFAOYSA-N
- Pubchem - 5807-14-7
- Wikipedia - 3,4,6,7,8,9-hexahydro-2H-pyrimido[1,2-a]pyrimidine
Triazabicyclodecene (1,5,7-Triazabicyclo[4.4.0]dec-5-ene or TBD) is a commercially available bicyclic strong guanidine base (pKa=25.98 in CH3CN and pKa=21.00 in THF). TBD is an organic soluble base which has been used effectively for a variety of base-mediated organic transformations such as: Michael reactions, Henry (nitroaldol reactions), Wittig reactions, HornerWadsworthEmmons reactions, transesterification reactions, etherifications, ring-opening polymerizations (Scheme 1), tautomerizations and epimerizations PC and PN bond formations, Knoevenagel condensations, deprotonation reactions of phenols, carboxylic acids and C-acids (Scheme 2), aminolysis of esters. It is also known in deprotonated form (at the 7-position), often as a ligand, for instance in Ditungsten tetra(hpp)
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