Chemical Synthesis

3-Thiopheneacrylic Acid is a synthetic intermediate.

3-Thiopheneacrylic Acid methyl ester is a synthetic intermediate.

3-Thiopheneacrylic Acid methyl ester is a synthetic intermediate.

3A-Amino-3A-deoxy-(2AS,3AS)-α-cyclodextrin Hydrate.

3N-Benzyloxycarbonyl 3-Amino-2,2-dimethylpropanamide is an intermediate in the synthesis of aliskiren. Aliskiren is a renin inhibitor which interacts with the renin-angiotensin system. Renin catalyzes the cleavage between angiotensinogen and

4′,4″(5″)-Di-tert-butyldicyclohexano-18-crown-6 is a lipophilic crown ether compound used in extraction chromatography for separation of strontium from nitric acid media. 4′,4″(5″)-Di-tert-butyldicyclohexano-18-crown-6 as a solution in 1-octanol is

4′,4″(5″)-Di-tert-butyldicyclohexano-18-crown-6 is a lipophilic crown ether compound used in extraction chromatography for separation of strontium from nitric acid media. 4′,4″(5″)-Di-tert-butyldicyclohexano-18-crown-6 as a solution in 1-octanol is

4′,4″(5″)-Di-tert-butyldicyclohexano-18-crown-6 is a lipophilic crown ether compound used in extraction chromatography for separation of strontium from nitric acid media. 4′,4″(5″)-Di-tert-butyldicyclohexano-18-crown-6 as a solution in 1-octanol is

4′,4″(5″)-Di-tert-butyldicyclohexano-18-crown-6 is a lipophilic crown ether compound used in extraction chromatography for separation of strontium from nitric acid media. 4′,4″(5″)-Di-tert-butyldicyclohexano-18-crown-6 as a solution in 1-octanol is

4′,4″(5″)-Di-tert-butyldibenzo-18-crown-6 is a hydrophobic crown ether compound. This crown ether is potentially useful in studies of ion transport through non-polar regions and membranes, and has been described in the design of microsensor devices

4′-Aminobenzo-18-crown-6 is a cyclic compound. It is widely used as an ionophore. It coordinates with metal ions more readily than other ligands because of its planar oxygen atoms which provide a strong negative potential

4′-Aminobenzo-18-crown-6 is a cyclic compound. It is widely used as an ionophore. It coordinates with metal ions more readily than other ligands because of its planar oxygen atoms which provide a strong negative potential