1152314-69-6

Basic information

• Product Name: 1-(naphthalene-2-yl)-2-(4-phenyl-1H-1,2,3-triazol-1-yl)ethan-1-one
• Synonyms: 1-(naphthalene-2-yl)-2-(4-phenyl-1H-1,2,3-triazol-1-yl)ethan-1-one
• CAS NO: 1152314-69-6
• Molecular Weight: 313.359
• Mol File: 1152314-69-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-(naphthalene-2-yl)-2-(4-phenyl-1H-1,2,3-triazol-1-yl)ethan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(naphthalene-2-yl)-2-(4-phenyl-1H-1,2,3-triazol-1-yl)ethan-1-one(1152314-69-6)
• EPA Substance Registry System: 1-(naphthalene-2-yl)-2-(4-phenyl-1H-1,2,3-triazol-1-yl)ethan-1-one(1152314-69-6)

Safety Data

• Hazardous Substances Data: 1152314-69-6(Hazardous Substances Data)

Upstream product

• 536-74-3 phenylacetylene 
• 613-54-7 2-Bromo-2'-acetonaphthone 
• 55117-00-5 2-azido-1-(2-naphthyl)ethanone 
• 352517-79-4 1-(2-Naphthyl)-2-(p-tolylsulfonyloxy)ethanone 

Downstream Products

• 1628223-91-5 1-allyl-2'-amino-6'-(naphthalen-2-yl)-2-oxo-5'-(4-phenyl-1H-1,2,3-triazol-1-yl)spiro[indoline-3,4'-pyran]-3'-carbonitrile 
• 1628223-90-4 2'-amino-5-chloro-6'-(naphthalen-2-yl)-2-oxo-5'-(4-phenyl-1H-1,2,3-triazol-1-yl)spiro[indoline-3,4'-pyran]-3'-carbonitrile 
• 1628223-89-1 2'-amino-5-bromo-6'-(naphthalen-2-yl)-2-oxo-5'-(4-phenyl-1H-1,2,3-triazol-1-yl)spiro[indoline-3,4'-pyran]-3'-carbonitrile 
• 1628224-02-1 2-amino-4-(4-bromophenyl)-6-(naphthalen-2-yl)-5-(4-phenyl-1H-1,2,3-triazol-1-yl)-4H-pyran-3-carbonitrile 

Relevant articles and documents

Catalytic asymmetric synthesis of β-triazolyl amino alcohols by asymmetric transfer hydrogenation of α-triazolyl amino alkanones

The synthesis of optically active β-triazolyl amino alcohols was carried out via ruthenium catalyzed asymmetric transfer hydrogenation of α-triazolyl amino alkanones. This reaction proceeds under mild reaction conditions with up to 99% yield and 99.9% ena

InCl3-mediated eco-friendly three-component domino reaction for synthesis of highly functionalized triazolylspiroxindolinopyrans and triazolylpyrans under solvent-free conditions

A one pot domino protocol has been developed for the efficient synthesis of novel triazolylspiroxindolinopyrans and triazolylpyran derivatives. The synthesis was achieved by reacting phenacyltriazole, isatin/aromatic aldehyde and active methylene compounds in the presence of InCl3 under solvent-free conditions at 100 °C. This novel strategy affording biologically relevant heterocyclic compounds presumably involves Knoevenagel condensation/Michael addition/6-exo-dig-cyclisation sequences. the Partner Organisations 2014.

A facile and regioselective synthesis of 1,4-disubstituted 1,2,3-triazoles using click chemistry

The reaction of α-tosyloxy ketones, sodium azide, and terminal alkynes in presence of copper(I) in aqueous polyethylene glycol afforded regioselectively 1,4-disubstituted 1,2,3-triazoles in good yield at ambient temperature. The one-pot exclusive formatio