Fine Chemicals and Lab Reagents

Application Enantioselective allylic substitution, enantioselective 1,3-dipolar cycloaddition.

Application Enantioselective allylic substitution, enantioselective 1,3-dipolar cycloaddition.

( S )-(+)-1-Amino-2-propanol is a chiral amino alcohol. Application ( S )-(+)-1-Amino-2-propanol may be used in the preparation of S -(+)-1-(2,3-naphthalimido)-2-propanol.

( S )-(+)-1-Amino-2-propanol is a chiral amino alcohol. Application ( S )-(+)-1-Amino-2-propanol may be used in the preparation of S -(+)-1-(2,3-naphthalimido)-2-propanol.

Application ( S )-(+)-2-Amino-1-butanol is a chiral amino alcohol that may be used in the synthesis of ( S )-2-(6-benzylamino-9-isopropyl-9 H -purin-2-ylamino) butan-1-ol, an ( S )-enantiomer of roscovitine. It can also be used to synthesize

Application ( S )-(+)-2-Amino-1-butanol is a chiral amino alcohol that may be used in the synthesis of ( S )-2-(6-benzylamino-9-isopropyl-9 H -purin-2-ylamino) butan-1-ol, an ( S )-enantiomer of roscovitine. It can also be used to synthesize

Application ( S )-(+)-2-Amino-1-hexanol can be used in one of the key synthetic steps for the synthesis of house dust mite (HDM) peptidase allergen Der p 1 inhibitors.

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

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

(S)-(+)-2-Amino-4-phenylbutyric acid ethyl ester hydrochloride

(S)-(+)-2-Phenylglycine methyl ester hydrochloride

(S)-(+)-2-Phenylglycine methyl ester hydrochloride