90923-99-2

Basic information

• Product Name: propargyl anthranilate
• Synonyms: propargyl anthranilate
• CAS NO: 90923-99-2
• Molecular Weight: 175.187
• Mol File: 90923-99-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: propargyl anthranilate(CAS DataBase Reference)
• NIST Chemistry Reference: propargyl anthranilate(90923-99-2)
• EPA Substance Registry System: propargyl anthranilate(90923-99-2)

Safety Data

• Hazardous Substances Data: 90923-99-2(Hazardous Substances Data)

Upstream product

• 118-48-9 isatoic anhydride 
• 107-19-7 propargyl alcohol 

Downstream Products

• 1415326-75-8 C₂₄H₂₈N₄O₁₁ 
• 1383577-44-3 prop-2-yn-1-yl 2-(4-([(2-azidophenyl)carbonyloxy]methyl)-1H-1,2,3-triazol-1-yl)benzoate 
• 1383577-58-9 [1-(2-([(1-(2-[(prop-2-yn-1-yloxy)carbonyl]phenyl)-1H-1,2,3-triazol-4-yl)methoxy]carbonyl)phenyl)-1H-1,2,3-triazol-4-yl]methyl 2-(4-([(2-azidophenyl)carbonyloxy]methyl)-1H-1,2,3-triazol-1-yl)benzoate 
• 1383577-57-8 [1-(2-([(1-(2-[(prop-2-yn-1-yloxy)carbonyl]phenyl)-1H-1,2,3-triazol-4-yl)methoxy]carbonyl)phenyl)-1H-1,2,3-triazol-4-yl]methyl 2-(4-([(2-aminophenyl)carbonyloxy]methyl)-1H-1,2,3-triazol-1-yl)benzoate 
• 1383577-56-7 2-(4-[((2-[4-(([2-(4-([(2-aminophenyl)carbonyloxy]methyl)-1H-1,2,3-triazol-1-yl)phenyl]carbonyloxy)methyl)-1H-1,2,3-triazol-1-yl]phenyl)carbonyloxy)methyl]-1H-1,2,3-triazol-1-yl)benzoic acid 
• 1383577-53-4 (1-{2-[(prop-2-yn-1-yloxy)carbonyl]phenyl}-1H-1,2,3-triazol-4-yl)methyl 2-(4-{[(2-aminophenyl)carbonyloxy]methyl}-1H-1,2,3-triazol-1-yl)benzoate 
• 1383577-47-6 2-(4-([(2-aminophenyl)carbonyloxy]methyl)-1H-1,2,3-triazol-1-yl)benzoic acid 
• 1383577-52-3 2-[4-(([2-(4-([(2-aminophenyl)carbonyloxy]methyl)-1H-1,2,3-triazol-1-yl)phenyl]carbonyloxy)methyl)-1H-1,2,3-triazol-1-yl]benzoic acid 

Relevant articles and documents

Propargyl anthranilate derivatives and their application in the synthesis of rings containing 1,2,3-triazolo motifs

Propargyl anthranilate, a simple and less studied molecule with several reactive sites, is widely applicable in organic synthesis. An optimized synthesis of this compound and its derivatives and the preparation of azide derivatives are described. The optimized process of the known intramolecular cyclization is described, and the unknown intermolecular cyclizations of these azido derivatives and formation of a macrocycle are discussed.

SYNTHESIS OF -TRIAZOLOBENZOXAZEPINES via INTRAMOLECULAR AZIDE CYCLOADDITION

Starting from isatoic anhydride and propargyl alcohols, we developed a synthetic approach to the title compounds, were the key step is an intramolecular cycloaddition of the azido group onto the acetylenic bond.