Glyoxal-bis(mesitylimine)

Glyoxal-bis(mesitylimine)
Names
	IUPAC name 2,4,6-Trimethyl-N-[(2E)-2-[(2,4,6-trimethylphenyl)imino]ethylidene]aniline
Identifiers
CAS Number	56222-36-7;
3D model (JSmol)	Interactive image;
ChemSpider	2971578;
PubChem CID	3741651;
CompTox Dashboard (EPA)	DTXSID00395802 ;
	InChI InChI=1S/C20H24N2/c1-13-9-15(3)19(16(4)10-13)21-7-8-22-20-17(5)11-14(2)12-18(20)6/h7-12H,1-6H3/b21-7+,22-8+ Key: YVKAJRYLHIECOK-KVJLFNRQSA-N;
	SMILES CC1=CC(C)=C(\N=C\C=N\C2=C(C)C=C(C)C=C2C)C(C)=C1;
Properties
Chemical formula	C20H24N2
Molar mass	292.426 g·mol−1
Appearance	Yellow solid
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

Glyoxal-bis(mesitylimine) is an organic compound with the formula H₂C₂(NC₆H₂Me₃)₂. It is a yellow solid that is soluble in organic solvents. It is classified as a diimine ligand. It is used in coordination chemistry and homogeneous catalysis. It is synthesized by condensation of 2,4,6-trimethylaniline and glyoxal.[1][2]

References

Ison, Elon A.; Ison, Ana (2012). "Synthesis of Well-Defined CopperN-Heterocyclic Carbene Complexes and Their Use as Catalysts for a "Click Reaction": A Multistep Experiment That Emphasizes the Role of Catalysis in Green Chemistry". Journal of Chemical Education. 89 (12): 1575–1577. Bibcode:2012JChEd..89.1575I. doi:10.1021/ed300243s.
Chen, Junting; Ritter, Tobias (2019). "Late-Stage Deoxyfluorination of Phenols with PhenoFluorMix". Org. Synth. 96: 16. doi:10.15227/orgsyn.096.0016.

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