Reagents for Peptide Synthesis

N(alpha)-boc-L-arginine

N(α), N-(im)-Di-Boc-L-histidine methyl ester

Product DescriptionN,N'-Dibenzoyl-L-cystine chiral modifier of LiBH4 for enantioselective reductions of heteroaromatic , aromatic, and unsaturated ketones to alcohols.Product ApplicationReactant involved in:Synthesis of integrin

Product DescriptionN,N'-Dibenzoyl-L-cystine chiral modifier of LiBH4 for enantioselective reductions of heteroaromatic , aromatic, and unsaturated ketones to alcohols.Product ApplicationReactant involved in:Synthesis of integrin

Product DescriptionN,N'-Dibenzoyl-L-cystine chiral modifier of LiBH4 for enantioselective reductions of heteroaromatic , aromatic, and unsaturated ketones to alcohols.Product ApplicationReactant involved in:Synthesis of integrin

Application：DCC ( N , N ′-Dicyclohexylcarbodiimide) is mainly used to mediate peptide coupling and also to activate carboxylic acids for esterification.

Reagent for preparing active esters of N-protected amino acids and for the preparation of protected dipeptides in good yields (1-2).

Reagent for preparing active esters of N-protected amino acids and for the preparation of protected dipeptides in good yields (1-2).

Reactant for: Synthesis of onium salts for use in peptide coupling Synthesis of safer replacement for coupling reagents Synthesis of cancer cell cytotoxins Synthesis of bioconjugation reagent

Reactant for: Synthesis of onium salts for use in peptide coupling Synthesis of safer replacement for coupling reagents Synthesis of cancer cell cytotoxins Synthesis of bioconjugation reagent

Reactant for: Synthesis of onium salts for use in peptide coupling Synthesis of safer replacement for coupling reagents Synthesis of cancer cell cytotoxins Synthesis of bioconjugation reagent

N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-S-(tert-butylthio)-L-cysteine