Di-tert-butyl dicarbonate

<strong>Di-tert-butyl dicarbonate</strong>_x000D_ <strong>Catalog number:</strong> B2015002_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> 218.25_x000D_ <strong>Supplied as:</strong> Powder_x000D_ <strong>Applications:</strong> molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> 2-8 °C_x000D_ <strong>Keywords:</strong> Boc2O, Boc anhydride, Di-tert-butyl pyrocarbonate_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: Kaur A, Pannu A, Brar DS, Mehta SK, Salunke DB. Yb(OTf)(3)-Catalyzed and Di-tert-butyl Dicarbonate-Mediated Decarboxylative Etherification and Esterification Reactions ACS Omega. 2020 Aug 13;5(33):21007-21014._x000D_ 2: Chen H, Li P, Qin R, Yan H, Li G, Huang H. DMAP-Catalyzed One-Pot Synthesis of Quinazoline-2,4-diones from 2-Aminobenzamides and Di-tert_butyl Dicarbonate ACS Omega. 2020 Apr 16;5(16):9614-9623._x000D_ 3: Basel Y, Hassner A. Di-tert-butyl dicarbonate and 4-(dimethylamino)pyridine revisited. Their reactions with amines and alcohols J Org Chem. 2000 Oct 6;65(20):6368-80._x000D_ 4: Applewhite MJ. tert-Butyl 4-cyano-phenyl carbonate Acta Crystallogr Sect E Struct Rep Online. 2010 Sep 30;66(Pt 10):o2681._x000D_ 5: Mohapatra DK, Datta A. Di-tert-butyl Dicarbonate: A Novel Reagent for the Efficient Synthesis of Dipeptides under Mild Conditions J Org Chem. 1999 Sep 3;64(18):6879-6880._x000D_ 6: Thrinadh Kumar R, Makam P, Katari NK, Kottalanka RK. A new synthetic approach to cyclic ureas through carbonylation using di-tert_butyl dicarbonate (boc anhydride) via one pot strategy Org Biomol Chem. 2023 Oct 4;21(38):7821-7830._x000D_ 7: Bartoli G, Bosco M, Carlone A, Dalpozzo R, Locatelli M, Melchiorre P, Sambri L. Alcohols and di-tert-butyl dicarbonate: how the nature of the Lewis acid catalyst may address the reaction to the synthesis of tert-butyl ethers J Org Chem. 2006 Dec 22;71(26):9580-8._x000D_ 8: Hong X, Wang H, Liu B, Xu B. Ruthenium-catalyzed double-fold C-H tertiary alkoxycarbonylation of arenes using di-tert-butyl dicarbonate Chem Commun (Camb). 2014 Nov 25;50(91):14129-32._x000D_ 9: Harris RB, Wilson IB. tert.-Butyl aminocarbonate (tert.-butyloxycarbonyloxyamine)--a new acylating reagent for amines Int J Pept Protein Res. 1984 Jan;23(1):55-60._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/1002132">10: Moroder L, Hallett A, Wünsch E, Keller O, Wersin G. [Di-tert.-butyl-dicarbonate, a useful tert.-Butyloxycardonylating reagent (author's transl)] Hoppe Seylers Z Physiol Chem. 1976 Nov;357(11):1651-3.</a>_x000D_ _x000D_ <strong>Products Related to Di-tert-butyl dicarbonate can be found at</strong> <a href="https://moleculardepot.com/product-category/Chemicals/"> Chemicals</a>