This is an old revision of this page, as edited by Smokefoot (talk | contribs) at 01:02, 13 December 2024 (1575 refs in SFS). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.
Revision as of 01:02, 13 December 2024 by Smokefoot (talk | contribs) (1575 refs in SFS)(diff) ← Previous revision | Latest revision (diff) | Newer revision → (diff)Identifiers | |
---|---|
CAS Number | |
ECHA InfoCard | 100.009.673 |
CompTox Dashboard (EPA) | |
Properties | |
Chemical formula | C21H21N |
Molar mass | 287.406 g·mol |
Appearance | white solid |
Melting point | 91.5 °C (196.7 °F; 364.6 K) |
Boiling point | 385 °C (725 °F; 658 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references |
Tribenzylamine is an organic compound with the formula N(CH2C6H5)3. It is a symmetrical tertiary amine. It is of some historic interest as one of the first compounds produced by the Leuckart reaction.
The compound is a common test target in methods development, e.g. from benzyl alcohol.
References
- Hamid, M. Haniti S. A.; Allen, C. Liana; Lamb, Gareth W.; Maxwell, Aoife C.; Maytum, Hannah C.; Watson, Andrew J. A.; Williams, Jonathan M. J. (2009). "Ruthenium-Catalyzed N -Alkylation of Amines and Sulfonamides Using Borrowing Hydrogen Methodology". Journal of the American Chemical Society. 131 (5): 1766–1774. Bibcode:2009JAChS.131.1766H. doi:10.1021/ja807323a. PMID 19191700.
- Kawahara, Ryoko; Fujita, Ken-Ichi; Yamaguchi, Ryohei (2010). "Multialkylation of Aqueous Ammonia with Alcohols Catalyzed by Water-Soluble Cp*Ir−Ammine Complexes". Journal of the American Chemical Society. 132 (43): 15108–15111. Bibcode:2010JAChS.13215108K. doi:10.1021/ja107274w. PMID 20931960.