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Allyl b-D-Lactose (Highly Pure)

<strong>Allyl b-D-Lactose (Highly Pure)</strong>_x000D_ <strong>Catalog number:</strong> B2012996_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 100 mg_x000D_ <strong>Molecular Weight or Concentration:</strong> 382.4 g/mol_x000D_ <strong>Supplied as:</strong> Lyophilized Powder_x000D_ <strong>Applications:</strong> molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> RT_x000D_ <strong>Keywords:</strong> Lactose_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: Junk L, Kazmaier U. The Allylic Alkylation of Ketone Enolates ChemistryOpen. 2020 Sep 10;9(9):929-952._x000D_ 2: Horino Y, Korenaga T. Versatile Reactivity of Metalloid-Substituted π-Allylpalladium Species Chem Rec. 2021 Dec;21(12):3911-3924._x000D_ 3: Jeon J, Cheon CH. Asymmetric Total Synthesis of Iheyamine B Org Lett. 2022 Oct 7;24(39):7128-7133._x000D_ 4: Ariyarathna Y, Tunge JA. Multicomponent decarboxylative allylations Chem Commun (Camb). 2014 Nov 21;50(90):14049-52._x000D_ 5: Rossi-Ashton JA, Clarke AK, Donald JR, Zheng C, Taylor RJK, Unsworth WP, You SL. Iridium-Catalyzed Enantioselective Intermolecular Indole C2-Allylation Angew Chem Int Ed Engl. 2020 May 4;59(19):7598-7604._x000D_ 6: Ou P, Zhu L, Yu Y, Ma L, Huang X. Palladium-Catalyzed Three-Component Selective Aminoallylation of Diazo Compounds Org Lett. 2022 Jun 17;24(23):4160-4164._x000D_ 7: Tang Q, Fu K, Ruan P, Dong S, Su Z, Liu X, Feng X. Asymmetric Catalytic Formal 1,4-Allylation of β,γ-Unsaturated α-Ketoesters: Allylboration/Oxy-Cope Rearrangement Angew Chem Int Ed Engl. 2019 Aug 19;58(34):11846-11851._x000D_ 8: Spaltenstein P, Cummins EJ, Yokuda KM, Kowalczyk T, Clark TB, O'Neil GW. Chemoselective Carbonyl Allylations with Alkoxyallylsiletanes J Org Chem. 2019 Apr 5;84(7):4421-4428._x000D_ 9: Zhang ZZ, Liao G, Chen HM, Shi BF. Thioamide-Directed Cp*Co(III)-Catalyzed C-H Allylation of Ferrocenes Org Lett. 2021 Apr 2;23(7):2626-2631._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/32721056">10: Chen WW, Cunillera A, Chen D, Lethu S, López de Moragas A, Zhu J, Solà M, Cuenca AB, Shafir A. Iodane-Guided ortho C-H Allylation Angew Chem Int Ed Engl. 2020 Nov 2;59(45):20201-20207. </a>_x000D_ _x000D_ <strong>Products Related to Allyl b-D-Lactose (Highly Pure) can be found at</strong> <a href="https://moleculardepot.com/product-category/Carbohydrates/"> Carbohydrates</a>

Product Specifications

Short Description

Catalog Number: B2012996 (100 mg)

Weight

0.15

Length

2

Width

0.5

Height

0.5

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