![1,8-Diazabicyclo[5.4.0]undec-7-ene](https://veeprho.com/wp-content/uploads/2022/07/1-8-Diazabicyclo5B5.4.05Dundec-7-ene-sqr.png "1,8-Diazabicyclo[5.4.0]undec-7-ene")
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0 % Toleranz bei der Produktqualität
Lagerstandorte
- New Jersey, USA
- Czech Republic, EU
- Mumbai, India
* Vorbehaltlich Verfügbarkeit
Dokumentation
Enthält: HPLC, MASS/LC-MS, 1H-NMR, FT-IR, Gehalt, Structure Elucidation Report (SER) sowie zusätzliche analytische Daten je nach Produkt.
6674-22-21,8-Diazabicyclo[5.4.0]undec-7-ene
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| Katalog-Nr.:: | VE008082 |
|---|---|
| CAS-Nr.:: | 6674-22-2 |
| Summenformel:: | C9H16N2 |
| Molare Masse:: | 152.24 g/mol |
Zusätzliche Informationen zu CAS 6674-22-2
Parent drug
TofacitinibIUPAC-Name
2, 3, 4, 6, 7, 8, 9, 10-octahydropyrimido[1, 2-a]azepinePharmakopöe-Synonyme
N/AOther Synonyms
1,8-Diaza-7-bicyclo[5.4.0]undecene; 1,8-Diazabicyclo[5.4.0]undecene-7SMILES
C2CCC1=NCCCN1CC2InChI
InChI=1S/C9H16N2/c1-2-5-9-10-6-4-8-11(9)7-3-1/h1-8H2Shipping Condition
Ambient TemperatureCharacterization Data (Included)
HPLC, MASS/LC-MS, 1H NMR, FT-IR, Potency, and Structure Elucidation Report (SER).Additional Characterization Data
QNMR, D2O Exchange, 13C NMR, 13C APT, COSY NMR, NOESY NMR, 15N NMR, HSQC NMR, HMQC NMR, and HMBC NMR. These are available upon request and may be free or subject to additional charges.Beschreibung
1,8-Diazabicyclo[5.4.0]undec-7-ene (CAS No: 6674-22-2) shows excellent catalytic activity in the Baylis–Hillman reaction. DBU is studied as a promoter for the aza-Michael reaction mainly used for constructing b-aminocarbonyl compounds. B-aminocarbonyl compounds are utilized as building blocks for various nitrogen-containing biologically essential compounds.References
Yeom, Chang-Eun, et al. “1, 8-Diazabicyclo[5.4.0]Undec-7-Ene (DBU)-Promoted Efficient and Versatile Aza-Michael Addition.” Tetrahedron, vol. 63, no. 4, Jan. 2007, pp. 904–9, https://doi.org/10.1016/j.tet.2006.11.037. ?Angebot anfordern
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