Lawesson Reagent

<strong>Lawesson Reagent</strong>_x000D_ <strong>Catalog number:</strong> B2012969_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> 404.5 g/mol_x000D_ <strong>Supplied as:</strong> Lyophilized Powder_x000D_ <strong>Applications:</strong> molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> 2-8°C_x000D_ <strong>Keywords:</strong> 2,4-Bis(4-methoxyphenyl)-2,4-dithioxo-1,3,2,4-dithiadiphosphetane, 2,4-Bis-(4-methoxyphenyl)-1,3-dithia-2,4-diphosphetane 2,4-disulfide, 4-Methoxyphenylthiophosphoric cyclic di(thioanhydride), LR_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: Khatoon H, Abdulmalek E. A Focused Review of Synthetic Applications of Lawesson's Reagent in Organic Synthesis Molecules. 2021 Nov 17;26(22):6937._x000D_ 2: Yin G, Wang X, Wang Y, Shi T, Zeng Y, Wang Y, Peng X, Wang Z. Lawesson's reagent promoted deoxygenation of azlactones for the syntheses of 2,4-disubstituted thiazoles Org Biomol Chem. 2022 Dec 14;20(48):9589-9592._x000D_ 3: Saeed A, Mehfooz H, Larik FA, Faisal M, Channar PA. Applications of Lawesson's reagent in the synthesis of naturally occurring steroids and terpenoids J Asian Nat Prod Res. 2017 Nov;19(11):1114-1123._x000D_ 4: Koval'skaya AV, Petrova PR, Tsypyshev DO, Lobov AN, Tsypysheva IP. Thionation of quinolizidine alkaloids and their derivatives via Lawesson's reagent Nat Prod Res. 2022 Jul;36(14):3538-3543._x000D_ 5: Wu K, Ling Y, Ding A, Jin L, Sun N, Hu B, Shen Z, Hu X. A chromatography-free and aqueous waste-free process for thioamide preparation with Lawesson's reagent Beilstein J Org Chem. 2021 Apr 9;17:805-812._x000D_ 6: Nicolau LA, Silva RO, Damasceno SR, Carvalho NS, Costa NR, Aragão KS, Barbosa AL, Soares PM, Souza MH, Medeiros JV. The hydrogen sulfide donor, Lawesson's reagent, prevents alendronate-induced gastric damage in rats Braz J Med Biol Res. 2013 Aug;46(8):708-14._x000D_ 7: Niijima E, Imai T, Suzuki H, Fujimoto Y, Kitagawa O. Thionation of Optically Pure N-C Axially Chiral Quinazolin-4-one Derivatives with Lawesson's Reagent J Org Chem. 2021 Jan 1;86(1):709-715._x000D_ 8: Huang P, Zhang R, Liang Y, Dong D. Lawesson's reagent-initiated domino reaction of aminopropenoyl cyclopropanes: synthesis of thieno[3,2-c]pyridinones Org Biomol Chem. 2012 Feb 28;10(8):1639-44._x000D_ 9: Kaleta Z, Makowski BT, Soós T, Dembinski R. Thionation using fluorous Lawesson's reagent Org Lett. 2006 Apr 13;8(8):1625-8._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/31943976">10: Giofrè SV, Mancuso R, Araniti F, Romeo R, Iannazzo D, Abenavoli MR, Gabriele B. Microwave-Assisted Synthesis of Sulfurated Heterocycles with Herbicidal Activity: Reaction of 2-Alkynylbenzoic Acids with Lawesson's Reagent Chempluschem. 2019 Jul;84(7):942-950. </a>_x000D_ _x000D_ <strong>Products Related to Lawesson Reagent can be found at</strong> <a href="https://moleculardepot.com/product-category/Chemicals/"> Chemicals</a>