(Benzotriazol-1-yloxy) tripyrrolidinophosphonium Hexafluorophosphate

<strong>(Benzotriazol-1-yloxy)tripyrrolidinophosphonium Hexafluorophosphate</strong>_x000D_ <strong>Catalog number:</strong> B2015866_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 250 mg_x000D_ <strong>Molecular Weight or Concentration:</strong> 520.39_x000D_ <strong>Supplied as:</strong> Powder_x000D_ <strong>Applications:</strong> a molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> 2-8°C_x000D_ <strong>Keywords:</strong> PyBOP®_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: Santos Oliveira AJM, de Castro RD, Pessôa HLF, Wadood A, de Sousa DP. Amides Derived from Vanillic Acid: Coupling Reactions, Antimicrobial Evaluation, and Molecular Docking Biomed Res Int. 2019 Apr 15;2019:9209676._x000D_ 2: Fauconnot L, Robert F, Villard R, Dionisi F. Chemical synthesis and NMR characterization of structured polyunsaturated triacylglycerols Chem Phys Lipids. 2006 Feb;139(2):125-36._x000D_ 3: Akula HK, Lakshman MK. Facile Modifications at the C4 Position of Pyrimidine Nucleosides via In Situ Amide Activation with 1H-Benzotriazol-1-yloxy-tris(dimethyl-amino)phosphonium Hexafluorophosphate Curr Protoc Nucleic Acid Chem. 2019 Mar;76(1):e73._x000D_ 4: Akula HK, Kokatla H, Andrei G, Snoeck R, Schols D, Balzarini J, Yang L, Lakshman MK. Facile functionalization at the C4 position of pyrimidine nucleosides via amide group activation with (benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate (BOP) and biological evaluations of the products Org Biomol Chem. 2017 Feb 1;15(5):1130-1139._x000D_ 5: Li P, Xu JC. (1H-benzotriazol-1-yloxy)-N,N-dimethylmethaniminium hexachloroantimonate (BOMI), a novel coupling reagent for solution and solid-phase peptide synthesis J Pept Res. 2000 Feb;55(2):110-9._x000D_ 6: Bae S, Lakshman MK. O6-(benzotriazol-1-yl)inosine derivatives: easily synthesized, reactive nucleosides J Am Chem Soc. 2007 Jan 31;129(4):782-9._x000D_ 7: Akula HK, Kokatla H, Andrei G, Snoeck R, Schols D, Balzarini J, Yang L, Lakshman MK. Correction: Facile functionalization at the C4 position of pyrimidine nucleosides via amide group activation with (benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate (BOP) and biological evaluations of the products Org Biomol Chem. 2017 Feb 1;15(5):1268._x000D_ 8: Khandaker TA, Hess JD, Aguilera R, Andrei G, Snoeck R, Schols D, Pradhan P, Lakshman MK. Synthesis and Evaluations of "1,4-Triazolyl Combretacoumarins" and Desmethoxy Analogues European J Org Chem. 2019 Sep 8;2019(33):5610-5623._x000D_ 9: Kokatla HP, Lakshman MK. Two-step, one-pot synthesis of inosine, guanosine, and 2'-deoxyguanosine O6-ethers via intermediate O6-(benzotriazol-1-yl) derivatives Curr Protoc Nucleic Acid Chem. 2012 Jun;Chapter 1:Unit1.26._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/19319856">10: Bae S, Chaturvedi S, Lakshman MK. O6-(benzotriazol-1-yl)inosine derivatives for C6 modification of purine nucleosides Curr Protoc Nucleic Acid Chem. 2009 Mar;Chapter 1:Unit 1.22. </a>_x000D_ _x000D_ <strong>Products Related to (Benzotriazol-1-yloxy)tripyrrolidinophosphonium Hexafluorophosphate can be found at</strong> <a href="https://moleculardepot.com/product-category/Chemicals/"> Chemicals</a>