Liquid Chromatography

Purity Limit: &ge 95% (HPLC) CAS No.: 889957-22-6 Molecular Formula: C8H9NO3 Molecular Weight: 167.16 MDL No.: MFCD03093399 Appearance: White solid Storage Temperature: Store at 0-8°C

Purity Limit: &ge 95% (HPLC) CAS No.: 889957-22-6 Molecular Formula: C8H9NO3 Molecular Weight: 167.16 MDL No.: MFCD03093399 Appearance: White solid Storage Temperature: Store at 0-8°C

(Rac)-CP-601927 hydrochloride is the racemate of CP-601927. CP-601927 is a nAChR agonist with Ki values 1.2 nM and 102 nM for α4β2 and α3β4 nAChR , respectively.In VitroCP-601927 induces significant antidepressant-like effects in mice. CP-601927

(Rac)-CP-601927 hydrochloride is the racemate of CP-601927. CP-601927 is a nAChR agonist with Ki values 1.2 nM and 102 nM for α4β2 and α3β4 nAChR , respectively.In VitroCP-601927 induces significant antidepressant-like effects in mice. CP-601927

(Rac)-CP-601927 hydrochloride is the racemate of CP-601927. CP-601927 is a nAChR agonist with Ki values 1.2 nM and 102 nM for α4β2 and α3β4 nAChR , respectively.In VitroCP-601927 induces significant antidepressant-like effects in mice. CP-601927

(S R S)-AHPC-CO-PEG1-C2-ACID

(S R S)-AHPC-CO-PEG4-C2-ACID

(S)-(+)-2-Amino-1-propanol may be used in the preparation of unsymmetrical tridentate Schiff base ligands via condensation with carbonyl compounds.[4] It may also be used as a chiral auxillary for the preparation of tert-butyl

(S)-(+)-2-Amino-1-propanol may be used in the preparation of unsymmetrical tridentate Schiff base ligands via condensation with carbonyl compounds.[4] It may also be used as a chiral auxillary for the preparation of tert-butyl

(S)-(+)-2-Amino-1-propanol may be used in the preparation of unsymmetrical tridentate Schiff base ligands via condensation with carbonyl compounds.[4] It may also be used as a chiral auxillary for the preparation of tert-butyl

(S)-(+)-2-Amino-1-propanol may be used in the preparation of unsymmetrical tridentate Schiff base ligands via condensation with carbonyl compounds.[4] It may also be used as a chiral auxillary for the preparation of tert-butyl

(S)-(+)-Isoleucinol