170169-51-4

Basic information

• Product Name: 3-((2E,4E)-5-phenylpenta-2,4-dienoyl)-2-hydroxy-2,4,6-cycloheptatrien-1-one
• Synonyms: 3-((2E,4E)-5-phenylpenta-2,4-dienoyl)-2-hydroxy-2,4,6-cycloheptatrien-1-one
• CAS NO: 170169-51-4
• Molecular Weight: 278.307
• Mol File: 170169-51-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-((2E,4E)-5-phenylpenta-2,4-dienoyl)-2-hydroxy-2,4,6-cycloheptatrien-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-((2E,4E)-5-phenylpenta-2,4-dienoyl)-2-hydroxy-2,4,6-cycloheptatrien-1-one(170169-51-4)
• EPA Substance Registry System: 3-((2E,4E)-5-phenylpenta-2,4-dienoyl)-2-hydroxy-2,4,6-cycloheptatrien-1-one(170169-51-4)

Safety Data

• Hazardous Substances Data: 170169-51-4(Hazardous Substances Data)

Upstream product

• 14371-10-9 (E)-3-phenylpropenal 
• 72023-82-6 3-acetyltropolone 

Downstream Products

• 1393645-92-5 C₁₈H₁₁Br₂NO₂ 
• 1393645-94-7 C₂₄H₁₇BrN₂O 
• 1393645-83-4 7-bromo-3-((2E,4E)-5-phenylpenta-2,4-dienoyl)tropolone 
• 1393645-84-5 5,7-dibromo-3-((2E,4E)-5-phenylpenta-2,4-dienoyl)tropolone 
• 1393645-85-6 7-iodo-3-((2E,4E)-5-phenylpenta-2,4-dienoyl)tropolone 
• 1393645-90-3 C₁₈H₁₃NO₂ 
• 1393645-91-4 C₁₈H₁₂BrNO₂ 
• 1393645-86-7 C₂₄H₁₈N₂O₃ 
• 1393645-87-8 C₂₅H₂₀N₂O₃ 
• 1393645-88-9 C₂₄H₁₇N₃O₅ 
• 1393645-93-6 C₂₄H₁₈N₂O 
• 1393645-96-9 C₂₅H₂₀N₂O₂ 
• 1393645-97-0 C₂₄H₁₇ClN₂O 
• 1393645-98-1 C₂₄H₁₇ClN₂O 

Relevant articles and documents

Synthesis of conjugated (E,E)-1,3-diene-containing troponoid-based compounds

Through exploration of the electrophilic substitution reaction of 3-((2E,4E)-5-phenylpenta-2,4-dienoyl)-2-hydroxy-2,4,6-cycloheptatrien-1-one (3-((2E,4E)-5-phenylpenta-2,4-dienoyl)tropolone) with halogen and diazonium salts as well as the nucleophilic cyclisation reaction with hydroxylamine hydrochloride and substituted phenylhydrazine hydrochlorides by employing our reliable methods, we have synthesised a series of new (E,E)-1,3-diene-bearing troponoid-based compounds. All the newly synthesised molecules represent an issue of great interest, since the presence of conjugated 1,3-diene moiety can be developed further via other reactions.