9-Azajulolidine (CAS 6052-72-8)
Alternate Names:
2,3,6,7-Tetrahydro-1H,5H-9-azabenzo[ij]quinolizine; 4,5,6,8,9,10-Hexahydropyrido[3,2,1-ij][1,6]naphthyridine
CAS Number:
6052-72-8
Molecular Weight:
174.24
Molecular Formula:
C11H14N2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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9-Azajulolidine is primarily utilized in research focused on heterocyclic chemistry, where its unique structure as a nitrogen-containing ring makes it a subject of interest. This compound is studied for its potential as a building block in the synthesis of more complex organic molecules, particularly pharmaceuticals and agrochemicals. Researchers explore the reactivity of 9-Azajulolidine to understand its behavior under various chemical conditions and its ability to form bonds with other functional groups. Additionally, its role in catalysis is investigated, particularly in reactions that require the formation of nitrogen-containing compounds.
9-Azajulolidine (CAS 6052-72-8) References
- A concise synthesis of 3-aroylflavones via Lewis base 9-azajulolidine-catalyzed tandem acyl transfer-cyclization. | Yoshida, M., et al. 2012. Chem Commun (Camb). 48: 11796-8. PMID: 23114707
- Annelated pyridines as highly nucleophilic and Lewis basic catalysts for acylation reactions. | Tandon, R., et al. 2013. Chemistry. 19: 6435-42. PMID: 23504953
- Rapid assembly of complex cyclopentanes employing chiral, α,β-unsaturated acylammonium intermediates. | Liu, G., et al. 2013. Nat Chem. 5: 1049-57. PMID: 24256870
- Enantiomeric Separation of Monosubstituted Tryptophan Derivatives and Metabolites by HPLC with a Cinchona Alkaloid-Based Zwitterionic Chiral Stationary Phase and Its Application to the Evaluation of the Optical Purity of Synthesized 6-Chloro-l-Tryptophan. | Fukushima, T., et al. 2015. Int J Tryptophan Res. 8: 1-5. PMID: 25624766
- Enantioselective acyl transfer catalysis by a combination of common catalytic motifs and electrostatic interactions. | Mandai, H., et al. 2016. Nat Commun. 7: 11297. PMID: 27079273
- Substituent Effects in the Silylation of Secondary Alcohols: A Mechanistic Study. | Marin-Luna, M., et al. 2018. Chemistry. 24: 15052-15058. PMID: 30070735
- Size-dependent rate acceleration in the silylation of secondary alcohols: the bigger the faster. | Marin-Luna, M., et al. 2018. Chem Sci. 9: 6509-6515. PMID: 30310581
- Recent Advances in the Addition of Amide/Sulfonamide Bonds to Alkynes. | Zhao, F., et al. 2019. Molecules. 24: PMID: 30621120
- Facile Synthesis of Pyrrolyl 4-Quinolinone Alkaloid Quinolactacide by 9-AJ-Catalyzed Tandem Acyl Transfer-Cyclization of o-Alkynoylaniline Derivatives. | Saito, K., et al. 2017. ACS Omega. 2: 4370-4381. PMID: 31457730
- Storage and release of two electrons from an electron-rich carbon-carbon bond: boron mediated reversible coupling of DMAP and 9-azajulolidine. | Cui, Y., et al. 2020. Chem Commun (Camb). 56: 6794-6797. PMID: 32432259
- First Total Synthesis and in Vitro Cytotoxicities of Flavesines G and J. | Pelss, J. and Smits, G. 2020. ACS Omega. 5: 12568-12572. PMID: 32548440
- On-demand synthesis of phosphoramidites. | Sandahl, AF., et al. 2021. Nat Commun. 12: 2760. PMID: 33958587
- Facile synthesis of 9-azajulolidine and its application to post-Ullmann reactions | KT Wong, SY Ku, FW Yen - Tetrahedron letters, 2007 - Elsevier. 16 July 2007,. Tetrahedron Letters. Volume 48, Issue 29,: Pages 5051-5054.
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| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
9-Azajulolidine, 250 mg | sc-472496 | 250 mg | $197.00 |