Modified Phosphoramidites

Product Application：3,5-Diiodosalicylaldehyde has been used in the synthesis of: new Schiff bases, (2,4-diiodo-6-[(2-morpholin-4-yl-ethylimino)-methyl]-phenol and 2,4-diiodo-6-[(3-morpholin-4-yl-propylimino)-methyl]-phenol) new tridentate ligand,

Product Application：3,5-Diiodosalicylaldehyde has been used in the synthesis of: new Schiff bases, (2,4-diiodo-6-[(2-morpholin-4-yl-ethylimino)-methyl]-phenol and 2,4-diiodo-6-[(3-morpholin-4-yl-propylimino)-methyl]-phenol) new tridentate ligand,

Application 3-Cyanophenylboronic acid can be used: As an intermediate in the synthesis of piperidine-based MCH R1 antagonists. As a substrate in the Suzuki coupling reactions to prepare 4-aryl-1,8-naphthyridin-2(1 H )-ones.

Application 4,4&#8242,4&#8243-Trimethoxytrityl chloride can be used: In one of the key synthetic steps for the preparation of two phosphoramidite building blocks. To prepare protein tagging molecule

Application 4,4&#8242,4&#8243-Trimethoxytrityl chloride can be used: In one of the key synthetic steps for the preparation of two phosphoramidite building blocks. To prepare protein tagging molecule

Biphenyl-4,4&#8242-disulfonyl chloride reacts with cycloinulohexaose in pyridine to form capped cyclofructan, 6 A ,6 C -di- O -(biphenyl-4,4&#8242-disulfonyl)-cycloinulohexaose . Application Biphenyl-4,4&#8242-disulfonyl chloride was used in the

Application 4-(Diethylamino)salicylaldehyde was used in the synthesis of Schiff-base ligand by monocondensation with diaminomaleonitrile .

Application 4-(Diethylamino)salicylaldehyde was used in the synthesis of Schiff-base ligand by monocondensation with diaminomaleonitrile .

Product Description：4-(Methylmercapto)phenol (4MP) mediates the removal of benzyloxycarbonyl and O-benzyl protecting groups by accepting the benzyl groups during the acidolytic cleavage with trifluoroacetic acid. The presence of hydroxyl group in

Product Description：4-(Methylmercapto)phenol (4MP) mediates the removal of benzyloxycarbonyl and O-benzyl protecting groups by accepting the benzyl groups during the acidolytic cleavage with trifluoroacetic acid. The presence of hydroxyl group in

Product Description：4-(Methylmercapto)phenol (4MP) mediates the removal of benzyloxycarbonyl and O-benzyl protecting groups by accepting the benzyl groups during the acidolytic cleavage with trifluoroacetic acid. The presence of hydroxyl group in

4-(3-Oxobutyl)phenyl acetate (4-(4-acetoxyphenyl) -2-butanone) is a standard melon fly attractant4-(3-Oxobutyl)phenyl acetate was used as attractant for detection programs aimed at melon fly and other cuelure-responding Bactrocera fruit flies.