1283850-69-0

Basic information

• Product Name: C₃₀H₂₇ClN₃O₂⁽¹⁺⁾
• Synonyms: C₃₀H₂₇ClN₃O₂⁽¹⁺⁾
• CAS NO: 1283850-69-0
• Molecular Weight: 497.016
• Mol File: 1283850-69-0.mol

Chemical Properties

• CAS DataBase Reference: C₃₀H₂₇ClN₃O₂⁽¹⁺⁾(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₀H₂₇ClN₃O₂⁽¹⁺⁾(1283850-69-0)
• EPA Substance Registry System: C₃₀H₂₇ClN₃O₂⁽¹⁺⁾(1283850-69-0)

Safety Data

• Hazardous Substances Data: 1283850-69-0(Hazardous Substances Data)

Upstream product

• 919102-70-8 (5aS,10bR)-5a,10b-dihydro-2-(2',4',6'-trimethylphenyl)-4H,6H-indeno[2,1-b]-1,2,4-triazolo[4,3-d]-1,4-oxazinium chloride monohydrate 
• 67228-76-6 4-chlorophenylpropynal 

Downstream Products

• 20754-21-6 methyl 3-(4-chlorophenyl)propenoate 
• 1615-02-7 3-(4-chlorophenyl)prop-2-enoic acid 
• 1232144-36-3 C₂₁H₂₅ClO₅Si 

Relevant articles and documents

α,β-Unsaturated acyl azoliums from N-heterocyclic carbene catalyzed reactions: Observation and mechanistic investigation

Caught in the act: Acyl azoliums have long been thought to be key reactive intermediates in N-heterocyclic carbene catalysis, but they have never been observed under catalytic conditions. Now, this has been successfully achieved by the characterization of α,β-unsaturated acyl azoliums (see scheme) using different spectroscopic techniques. Kinetic studies revealed the origin of their unexpected chemoselectivity in acylation and annulation reactions.