856422-37-2

Upstream product

• 875-74-1 (R)-phenylglycine 
• 65095-13-8 1-benzotriazolecarboxylic acid chloride 

Downstream Products

• 136459-36-4 (R)-[(Benzotriazole-1-carbonyl)-amino]-phenyl-acetyl chloride 
• 1248783-32-5 1-((2-hydroxyethylcarbamoyl)(phenyl)methyl)-3-(2-hydroxyethyl)urea 
• 1248783-33-6 1-((3-hydroxypropylcarbamoyl)(phenyl)methyl)-3-(3-hydroxypropyl)urea 
• 845786-72-3 N-(1-benzotriazolecarbonyl)-D-phenylglycine cyclohexanemethylamide 
• 845786-74-5 N-(1-benzotriazolecarbonyl)-D-phenylglycine diphenylmethylamide 
• 845786-71-2 N-(1-benzotriazolecarbonyl)-D-phenylglycine cyclohexylamide 
• 845786-73-4 N-(1-benzotriazolecarbonyl)-D-phenylglycine piperidineamide 
• 845786-75-6 N-(1-benzotriazolecarbonyl)-D-phenylglycine cyclopentylamide 

Relevant academic research and scientific papers

Hydantoin derivatives of L- and D-amino acids: Synthesis and evaluation of their antiviral and antitumoral activity

3,5-Disubstituted hydantoin (1,3-imidazolidinedione) derivatives 5a-h were prepared by base induced cyclization of the corresponding N-(1- benzotriazolecarbonyl)-L-and D-amino acid amides 4a-h. Compounds 5a-h were evaluated for their cytostatic and antivi

The novel L- and D-amino acid derivatives of hydroxyurea and hydantoins: Synthesis, X-ray crystal structure study, and cytostatic and antiviral activity evaluations

The novel L- and D-amino acid derivatives of hydroxyurea 5a-o were prepared by aminolysis of N-(1-benzotriazolecarbonyl)amino acid amides 4a-o with hydroxylamine. The hydantoin derivatives 6a-e,m,p were synthesized by base-catalyzed cyclization of amides