1394236-37-3

Basic information

• Product Name: 1-(4-(4-tetradecyloxybenzoyloxy)phenyl)-4-(4-(4-tetradecyloxybenzoyloxy)phenyl)-1H-1,2,3-triazol
• Synonyms: 1-(4-(4-tetradecyloxybenzoyloxy)phenyl)-4-(4-(4-tetradecyloxybenzoyloxy)phenyl)-1H-1,2,3-triazol
• CAS NO: 1394236-37-3
• Molecular Weight: 886.228
• Mol File: 1394236-37-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(4-(4-tetradecyloxybenzoyloxy)phenyl)-4-(4-(4-tetradecyloxybenzoyloxy)phenyl)-1H-1,2,3-triazol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-(4-tetradecyloxybenzoyloxy)phenyl)-4-(4-(4-tetradecyloxybenzoyloxy)phenyl)-1H-1,2,3-triazol(1394236-37-3)
• EPA Substance Registry System: 1-(4-(4-tetradecyloxybenzoyloxy)phenyl)-4-(4-(4-tetradecyloxybenzoyloxy)phenyl)-1H-1,2,3-triazol(1394236-37-3)

Safety Data

• Hazardous Substances Data: 1394236-37-3(Hazardous Substances Data)

Upstream product

• 2200-91-1 4-ethynylphenol 
• 144256-13-3 1,1-dibromo-2-(4-hydroxyphenyl)ethylene 
• 123-08-0 4-hydroxy-benzaldehyde 
• 123-30-8 4-amino-phenol 
• 1394236-23-7 4-azidophenyl 4-tetradecyloxybenzoate 
• 142663-61-4 4-ethynylphenyl 4-tetradecyloxybenzoate 

Relevant articles and documents

"Click chemistry" as a versatile route to synthesize and modulate bent-core liquid crystalline materials

Three series of bent-shaped compounds containing the 1,2,3-triazole ring in the central core of the molecule have been prepared by the most extended "click chemistry" reaction, the copper-catalyzed azide-alkyne cycloaddition (CuAAC). This research demonstrates the versatility of this synthetic approach with the aim of achieving innovative compact supramolecular organizations. The appropriate combination of the 1,2,3-triazole synthon linked either to a methylene unit (series M) or to a methylenoxycarbonyl block (series MC) has allowed the induction of a variety of non-classical bent-core liquid crystal phases versus the classic mesophases promoted by 1,4-diphenyl-1,2,3- triazole derivatives (series T). Through a suitable selection of common lateral structures connected by "click chemistry" both the transition temperatures and mesomorphism, ranging from lamellar to columnar or B4-like supramolecular liquid crystalline organizations, can be tuned. The Royal Society of Chemistry 2012.