1079362-29-0

Basic information

• Product Name: 4-methyl-7-({1-[4-(2-thienylcarbonyl)benzyl]-1H-1,2,3-triazol-4-yl}methoxy)-2H-chromen-2-one
• Synonyms: 4-methyl-7-({1-[4-(2-thienylcarbonyl)benzyl]-1H-1,2,3-triazol-4-yl}methoxy)-2H-chromen-2-one
• CAS NO: 1079362-29-0
• Molecular Weight: 457.51
• Mol File: 1079362-29-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-methyl-7-({1-[4-(2-thienylcarbonyl)benzyl]-1H-1,2,3-triazol-4-yl}methoxy)-2H-chromen-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methyl-7-({1-[4-(2-thienylcarbonyl)benzyl]-1H-1,2,3-triazol-4-yl}methoxy)-2H-chromen-2-one(1079362-29-0)
• EPA Substance Registry System: 4-methyl-7-({1-[4-(2-thienylcarbonyl)benzyl]-1H-1,2,3-triazol-4-yl}methoxy)-2H-chromen-2-one(1079362-29-0)

Safety Data

• Hazardous Substances Data: 1079362-29-0(Hazardous Substances Data)

Upstream product

• 1079362-22-3 [4-(azidomethyl)phenyl](2-thienyl)methanone 
• 67268-43-3 7-propargyloxy-4-methyl-2H-chromen-2-one 

Relevant articles and documents

Synthesis of potentially photoactivatable coumarin derivatives via a 1,3-dipolar cycloaddition

(Chemical Equation Presented) A copper (I)-catalyzed 1,3-dipolar cycloaddition reaction was used to prepare a series of mono and disubstituted 1,2,3-triazolyl-coumarins using a 1,3-cycloaddition ("Click Chemistry"). Starting coumarins were synthesized using classical or modified Pechmann's reaction. The propargyl group was introduced as either propargylether or as a propargylamide. Azides were prepared in a three steps procedure. Cycloaddition products, containing a coumarin and a photoactivatable moiety, were obtained in good yields.