Peptide Synthesis

Nanocs' amino acid and peptide PEG conjugates were made from the covalent attachment of PEG to various amino acid derivatives. Conjugates were provided in lyophilized powder form.

Nanocs' amino acid and peptide PEG conjugates were made from the covalent attachment of PEG to various amino acid derivatives. Conjugates were provided in lyophilized powder form.

Nanocs' amino acid and peptide PEG conjugates were made from the covalent attachment of PEG to various amino acid derivatives. Conjugates were provided in lyophilized powder form.

Nanocs' amino acid and peptide PEG conjugates were made from the covalent attachment of PEG to various amino acid derivatives. Conjugates were provided in lyophilized powder form.

4'-AMINO-2'-HYDROXY-N4-PROPIONYLSULFANILANILIDE

Application Catalyst for: Preparation of dicyano(aryl)cyclohexenecarboxylic acid esters via regioselective annulation Diastereoselective cycloaddition of styrenyl allenoates Interfacial carbonylation of methylbenzyl bromide Hydroformylation of

4-(N-Boc-amino)-1,6-heptanedioic acid is a branched PEG derivative with a Boc protected amino group and two terminal carboxylic acids. The protected amine can be deprotected by acidic conditions. The terminal carboxylic acids can be reacted with

4-(N-Boc-amino)-1,6-heptanedioic acid is a branched PEG derivative with a Boc protected amino group and two terminal carboxylic acids. The protected amine can be deprotected by acidic conditions. The terminal carboxylic acids can be reacted with

4-(N-Boc-amino)-1,6-heptanedioic acid is a branched PEG derivative with a Boc protected amino group and two terminal carboxylic acids. The protected amine can be deprotected by acidic conditions. The terminal carboxylic acids can be reacted with

A synthetic intermediate for pharmaceutical synthesis.

A synthetic intermediate for pharmaceutical synthesis.

A synthetic intermediate for pharmaceutical synthesis.