Drugs and Pharmaceutical Products

Made from natural tartaric acid Application (+)-Diethyl L -tartrate can be used in the synthesis of biologically active compounds such as (+)-altholactone , (-)-aspicilin , (+)-monomorine I and (+)-(1 R ,2 R ,3 S ,6 S )-3,6-di- O -methyl

(+)-Dihydrocarveol

(+)-Dihydrocarvone, a monoterpenoid compound found in caraway oil, is a key building block to synthesize sesquiterpenes. It is generally produced either by the hydrogenation of carvone or oxidation of limonene.

(+)-Dihydrocarvone (mixture of isomers) is a monoterpenoid compound, mainly used as a building block to prepare sesquiterpenes. Application The N -functionalization of dihydrocarvone forms imine derivatives, which are synthons for preparing N

(+)-Dimethyl 2,3- O -isopropylidene- D -tartrate is a chiral reagent used in organic synthesis. It is prepared by the reaction-rectification process from D -tartrate, and 2,2-dimethoxypropane.

Application (+)-Dimethyl L -tartrate can react with sulfur tetrafluoride to form dimethyl meso-2,3-difluorosuccinate. It may be used in the synthesis of the following chiral ligands for use in asymmetric synthesis: (2 R , 3 R

Application (+)-Dimethyl L -tartrate can react with sulfur tetrafluoride to form dimethyl meso-2,3-difluorosuccinate. It may be used in the synthesis of the following chiral ligands for use in asymmetric synthesis: (2 R , 3 R

Application Both (+)- and (-)-DIP-chloride are used for asymmetric reduction of prochiral ketones and for the preparation of &#946-amino alcohols. Excellent reagent for asymmetric reductions.

Application Both (+)- and (-)-DIP-chloride are used for asymmetric reduction of prochiral ketones and for the preparation of &#946-amino alcohols. Excellent reagent for asymmetric reductions.

for synthesis Application (+)-Ethyl-4,6-di-O-acetyl-2,3-dideoxy-&#945-D-erythro-hex-2- enopyranoside for synthesis. CAS 3323-72-6, molar mass 258.

(+)-Etomoxir sodium salt hydrate belongs to oxirane carboxylic acid group of compounds and mediates metabolic channeling of fatty acid precursors. It favors oxidative stress in T cells and prevents T cell differentiation.

(+)-Etomoxir sodium salt hydrate belongs to oxirane carboxylic acid group of compounds and mediates metabolic channeling of fatty acid precursors. It favors oxidative stress in T cells and prevents T cell differentiation.