Cyclohexanecarboxylic acids and phenethylamines

(2S,3S,4S)-2-Methyl-2-(carboxycyclopropyl)glycine is a selective antagonist of group II metabotropic glutamate receptor (mGluR). It has also been found to be a selective antagonist for presynaptic EAA receptors that are activated by (1S,3S)-ACPD and

(3aR,6R,6aR)-6-ethenyl-2,2-dimethyl-hexahydrocyclopenta[d][1,3]dioxol-4-one.

(3aR,6R,6aR)-6-ethenyl-2,2-dimethyl-hexahydrocyclopenta[d][1,3]dioxol-4-one.

(3aR,6R,6aR)-6-ethenyl-2,2-dimethyl-hexahydrocyclopenta[d][1,3]dioxol-4-one.

(7R,13R,17R)-17-[2-[4-(diethylaminomethyl)-2-methoxyphenoxy]ethyl]-7,13-dimethyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-ol:2-hydroxypropane-1,2,3-tricarboxylic acid.

Product Application：(R)-(+)-5,5′,6,6′,7,7′,8,8′-octahydro-1,1′-2-naphthol can be used:• As a starting material for the preparation of octahydro-binaphthyl based organic light-emitting diodes.• As a ligand in the 1,4-hydrophosphinylation of methyl

Product Application：(R)-(+)-5,5′,6,6′,7,7′,8,8′-octahydro-1,1′-2-naphthol can be used:• As a starting material for the preparation of octahydro-binaphthyl based organic light-emitting diodes.• As a ligand in the 1,4-hydrophosphinylation of methyl

Product Application：(R)-(+)-5,5′,6,6′,7,7′,8,8′-octahydro-1,1′-2-naphthol can be used:• As a starting material for the preparation of octahydro-binaphthyl based organic light-emitting diodes.• As a ligand in the 1,4-hydrophosphinylation of methyl

( R )-(-)-1-Cyclohexylethylamine is a chiral amine mainly used as a resolving agent for racemic compounds. Application ( R )-(-)-1-Cyclohexylethylamine may be used in the preparation of a chiral calix[4]arene Schiff base derivatives with potential

(R)-4-((3R,5R,8S,9S,10R,13R,14S,17R,E)-6-Ethylidene-3-hydroxy-10,13-dimethyl-7-oxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acid.

Catalyst involved in: ? [3,3]-Sigmatropic rearrangements using cyclopropane probes ? Asymmetric intramolecular hydroacylation of ketoaldehydes Reactant involved in: ? The synthesis of gold-diphosphine complexes for use as catalysts ? Cycloaddition

Catalyst involved in: ? [3,3]-Sigmatropic rearrangements using cyclopropane probes ? Asymmetric intramolecular hydroacylation of ketoaldehydes Reactant involved in: ? The synthesis of gold-diphosphine complexes for use as catalysts ? Cycloaddition