TargetMol

Tribenzylamine

Product Code:
 
TAR-T20323
Product Group:
 
Inhibitors and Activators
Supplier:
 
TargetMol
Regulatory Status:
 
RUO
Shipping:
 
cool pack
Storage:
 
-20℃
1 / 1
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CodeSizePrice
TAR-T20323-5mg5mg£850.00
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Further Information

Bioactivity:
Tribenzylamine is an agent of biochemical.
CAS:
620-40-6
Formula:
C21H21N
Molecular Weight:
287.406
Purity:
0.98
SMILES:
C(N(Cc1ccccc1)Cc1ccccc1)c1ccccc1

References

1. Mikata Y, Nodomi Y, Ohnishi R, Kizu A, Konno H. Tris(8-methoxy-2-quinolylmethyl)amine (8-MeOTQA) as a highly fluorescent Zn(2+) probe prepared by convenient C3-symmetric tripodal amine synthesis. Dalton Trans. 2015 May 7;44(17):8021-30. doi: 10.1039/c5dt00514k. PubMed PMID: 25827829. 2. Bortoluzzi M, Marchetti F, Pampaloni G, Zacchini S. Tribenzylamine C-H activation and intermolecular hydrogen transfer promoted by WCl6. Inorg Chem. 2014 Apr 7;53(7):3832-8. doi: 10.1021/ic5001683. Epub 2014 Mar 13. PubMed PMID: 24624963. 3. Lang X, Ma W, Zhao Y, Chen C, Ji H, Zhao J. Visible-light-induced selective photocatalytic aerobic oxidation of amines into imines on TiO2. Chemistry. 2012 Feb 27;18(9):2624-31. doi: 10.1002/chem.201102779. Epub 2012 Jan 23. PubMed PMID: 22271403. 4. Khan NS, Perez-Aguilar JM, Kaufmann T, Hill PA, Taratula O, Lee OS, Carroll PJ, Saven JG, Dmochowski IJ. Multiple hindered rotators in a gyroscope-inspired tribenzylamine hemicryptophane. J Org Chem. 2011 Mar 4;76(5):1418-24. doi: 10.1021/jo102480s. Epub 2011 Jan 27. PubMed PMID: 21271707; PubMed Central PMCID: PMC3045655.