Lamivudine sulfoxide

(+)-&#945-Pinene is a monoterpenoid compound mainly found in Pinus species. Application (+)-&#945-Pinene may be used as precursors to prepare primary, secondary and tertiary &#947-amino alcohols and 1,3-diamines, which can be used as chiral

(+)-&#945-Pinene is a monoterpenoid compound mainly found in Pinus species. Application (+)-&#945-Pinene may be used as precursors to prepare primary, secondary and tertiary &#947-amino alcohols and 1,3-diamines, which can be used as chiral

(+)-&#945-Pinene is a monoterpenoid compound, which comprises of an endocyclic double bond and is found in the resins of pine trees and other conifers. Application Refer to the product&#8242s Certificate of Analysis for more information on a

(+)-&#945-Pinene is a monoterpenoid compound, which comprises of an endocyclic double bond and is found in the resins of pine trees and other conifers. Application Refer to the product&#8242s Certificate of Analysis for more information on a

Application Relative stereochemistry

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including MSDS and any product information leaflets have been developed and issued under the Authority of the

Structure confirmed. Purity = 98%. Will ship with Certificate of Analysis (CoA)

Structure confirmed. Will ship with Certificate of Analysis (CoA)

Application Reactant for: Substitution reactions for synthesis of N-heterocyclic carbene boranes with boron-heteroatom bonds Hydroboration reactions Regio- and chemoselective brominative cleavage of terminal epoxides

Meet Stage 1 requirements for US EPA Methods 552, 552.1 and 552.

Internal Standard: cat.# 31648 Surrogates for Method 552, 552.1: cat.#&#39s 31650, 31652, 31649, 31651 Surrogates for Method 552.2: cat.#&#39s 31653, 31655, 31656 Surrogates for Method 552.3: cat.#&#39s 31881, 31882