5-Cyanoindole (Highly Pure)

<strong>5-Cyanoindole (Highly Pure)</strong>_x000D_ <strong>Catalog number:</strong> B2016217_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 5 g_x000D_ <strong>Molecular Weight or Concentration:</strong> 142.16 g/mol_x000D_ <strong>Supplied as:</strong> Powder_x000D_ <strong>Applications:</strong> a molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> -20°C_x000D_ <strong>Keywords:</strong> Indole-5-cyanonitrile_x000D_ <strong>Grade:</strong> Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity &gt;18 MΩ-cm) and are filtered through 0.22 um._x000D_ _x000D_ <strong>References:</strong>_x000D_ 1: Yokogawa D. Time-dependent density functional theory (TD-DFT) coupled with reference interaction site model self-consistent field explicitly including spatial electron density distribution (RISM-SCF-SEDD) J Chem Phys. 2016 Sep 7;145(9):094101._x000D_ 2: Waegele MM, Gai F. Computational Modeling of the Nitrile Stretching Vibration of 5-Cyanoindole in Water J Phys Chem Lett. 2010 Feb 1;1(4):781-786._x000D_ 3: Oeltermann O, Brand C, Engels B, Tatchen J, Schmitt M. The structure of 5-cyanoindole in the ground and the lowest electronically excited singlet states, deduced from rotationally resolved electronic spectroscopy and ab initio theory Phys Chem Chem Phys. 2012 Aug 7;14(29):10266-70._x000D_ 4: Yang Y, Liu J, Feng RR, Zhang W, Gai F. C≡N Stretching Frequency as a Convenient Reporter of Charge Separation in Molecular Systems J Phys Chem B. 2023 Aug 10;127(31):6999-7003._x000D_ 5: Stuhlmann B, Gräßle A, Schmitt M. Determination of the geometry change of 5-cyanoindole upon electronic excitation from a combined Franck-Condon/rotational constants fit Phys Chem Chem Phys. 2014 Jan 21;16(3):899-905._x000D_ 6: Markiewicz BN, Mukherjee D, Troxler T, Gai F. Utility of 5-Cyanotryptophan Fluorescence as a Sensitive Probe of Protein Hydration J Phys Chem B. 2016 Feb 11;120(5):936-44._x000D_ 7: Talbi H, Billaud D, Louarn G, Pron A. UV-vis and Raman spectroelectrochemical investigation of the redox behavior of poly(5-cyanoindole) in acidic aqueous solutions Spectrochim Acta A Mol Biomol Spectrosc. 2000 Mar;56(4):717-28._x000D_ 8: Hebestreit ML, Schneider M, Lartian H, Betz V, Heinrich M, Lindic M, Choi MY, Schmitt M. Structures, dipole moments and excited state lifetime of isolated 4-cyanoindole in its ground and lowest electronically excited singlet states Phys Chem Chem Phys. 2019 Jul 10;21(27):14766-14774._x000D_ 9: Lakhdar S, Westermaier M, Terrier F, Goumont R, Boubaker T, Ofial AR, Mayr H. Nucleophilic reactivities of indoles J Org Chem. 2006 Nov 24;71(24):9088-95._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/23448701">10: Yuen OY, Choy PY, Chow WK, Wong WT, Kwong FY. Synthesis of 3-cyanoindole derivatives mediated by copper(I) iodide using benzyl cyanide J Org Chem. 2013 Apr 5;78(7):3374-8. </a>_x000D_ _x000D_ <strong>Products Related to 5-Cyanoindole (Highly Pure) can be found at</strong> <a href="https://moleculardepot.com/product-category/Chemicals/"> Chemicals</a>