1612882-73-1

Basic information

• Product Name: (Z)-N-[3-(furan-2-ylmethyl)-4-({3-[4-(trifluoromethoxy)phenyl]-isoxazol-5-yl}methoxy)-4-(trifluoromethyl)thiazolidin-2-ylidene]-aniline
• Synonyms: (Z)-N-[3-(furan-2-ylmethyl)-4-({3-[4-(trifluoromethoxy)phenyl]-isoxazol-5-yl}methoxy)-4-(trifluoromethyl)thiazolidin-2-ylidene]-aniline
• CAS NO: 1612882-73-1
• Molecular Weight: 583.511
• Mol File: 1612882-73-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (Z)-N-[3-(furan-2-ylmethyl)-4-({3-[4-(trifluoromethoxy)phenyl]-isoxazol-5-yl}methoxy)-4-(trifluoromethyl)thiazolidin-2-ylidene]-aniline(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-N-[3-(furan-2-ylmethyl)-4-({3-[4-(trifluoromethoxy)phenyl]-isoxazol-5-yl}methoxy)-4-(trifluoromethyl)thiazolidin-2-ylidene]-aniline(1612882-73-1)
• EPA Substance Registry System: (Z)-N-[3-(furan-2-ylmethyl)-4-({3-[4-(trifluoromethoxy)phenyl]-isoxazol-5-yl}methoxy)-4-(trifluoromethyl)thiazolidin-2-ylidene]-aniline(1612882-73-1)

Safety Data

• Hazardous Substances Data: 1612882-73-1(Hazardous Substances Data)

Upstream product

• 103-72-0 phenyl isothiocyanate 
• 150162-39-3 N-hydroxy-1-[4-(trifluoromethoxy)phenyl]methaneimine 
• 617-89-0 furan-2-ylmethanamine 

Relevant articles and documents

One-pot synthesis of 2-imino-4-(trifluoromethyl)thiazolidin-4-ol derivatives in a three-component reaction: Application to structurally diverse scaffolds of biological interest through subsequent reactions

A highly efficient method for the synthesis of 2-imino-4-(trifluoromethyl) thiazolidin-4-ol derivatives has been achieved by the one-pot, three-component reactions of primary amines, aryl isothiocyanates, and 3-bromo-1,1,1- trifluoropropanone. The reactions go via symmetrical and unsymmetrical thiourea intermediates. Subsequent reactions of the products allow the synthesis of various scaffolds, including isoxazoles, triazoles, and propargylamine derivatives. A one-pot, three-component reaction for the synthesis of 2-imino-4-(trifluoromethyl)thiazolidin-4-ol derivatives is described. Subsequent reactions of the products allow the synthesis of various scaffolds, including isoxazoles, triazoles, and propargylamine derivatives. Copyright