1380328-61-9

Basic information

• Product Name: 4-((2-oxo-4-(trifluoromethyl)-2H-chromen-7-ylcarbamoyloxy)methyl)phenyl-3-mercapto-2-(2-(2-phenylacetamido)acetamido)propanoate
• Synonyms: 4-((2-oxo-4-(trifluoromethyl)-2H-chromen-7-ylcarbamoyloxy)methyl)phenyl-3-mercapto-2-(2-(2-phenylacetamido)acetamido)propanoate
• CAS NO: 1380328-61-9
• Molecular Weight: 657.624
• Mol File: 1380328-61-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-((2-oxo-4-(trifluoromethyl)-2H-chromen-7-ylcarbamoyloxy)methyl)phenyl-3-mercapto-2-(2-(2-phenylacetamido)acetamido)propanoate(CAS DataBase Reference)
• NIST Chemistry Reference: 4-((2-oxo-4-(trifluoromethyl)-2H-chromen-7-ylcarbamoyloxy)methyl)phenyl-3-mercapto-2-(2-(2-phenylacetamido)acetamido)propanoate(1380328-61-9)
• EPA Substance Registry System: 4-((2-oxo-4-(trifluoromethyl)-2H-chromen-7-ylcarbamoyloxy)methyl)phenyl-3-mercapto-2-(2-(2-phenylacetamido)acetamido)propanoate(1380328-61-9)

Safety Data

• Hazardous Substances Data: 1380328-61-9(Hazardous Substances Data)

Upstream product

• 103-80-0 phenylacetyl chloride 
• 126070-20-0 4-((tert-butyldimethylsilyloxy)methyl)phenol 
• 53518-15-3 Coumarin 151 
• 1380328-57-3 2-(2-(2-phenylacetamido)acetamido)-3-(tritylthio)propanoic acid 
• 1380328-56-2 methyl 2-(2-(2-phenylacetamido)acetamido)-3-(tritylthio)propanoate 
• 1380328-60-8 4-((2-oxo-4-(trifluoromethyl)-2H-chromen-7-ylcarbamoyloxy)methyl)phenyl 2-(2-(2-phenylacetamido)acetamido)-3-(tritylthio)propanoate 
• 500-98-1 phenylacetylglycine 

Downstream Products

• 1380328-55-1 C₆₁H₇₇F₃N₄O₂₁S₂ 

Relevant articles and documents

Development of a new enzyme-responsive self-immolative spacer conjugate applicable to the controlled drug release

A new self-immolative spacer conjugate based on a chemical adaptor unit aiming at controlled releasing drugs was designed and synthesized. It releases a fluorophore which was used as a model drug via a spontaneous cyclization mechanism after cleavage of an enzyme substrate. This system was proved to be stable under physiological conditions and only decomposed triggered by enzyme. It provides a generic linkage allowing connection of a variety of drugs and targeted devices to the chemical adaptor.