17159-98-7

Basic information

• Product Name: 2-Cyclohexen-1-one, 3-(4-methoxyphenyl)-
• CAS NO: 17159-98-7
• Molecular Formula: C13H14O2
• Molecular Weight: 202.253
• Mol File: 17159-98-7.mol
• Article Data: 36

Chemical Properties

• CAS DataBase Reference: 2-Cyclohexen-1-one, 3-(4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Cyclohexen-1-one, 3-(4-methoxyphenyl)-(17159-98-7)
• EPA Substance Registry System: 2-Cyclohexen-1-one, 3-(4-methoxyphenyl)-(17159-98-7)

Safety Data

• Hazardous Substances Data: 17159-98-7(Hazardous Substances Data)

Upstream product

• 5720-07-0 4-methoxyphenylboronic acid 
• 504-02-9 1,3-cylohexanedione 
• 930-68-7 cyclohexenone 
• 696-62-8 para-iodoanisole 
• 3128-06-1 5-ketohexanoic acid 
• 100-66-3 methoxybenzene 
• 35692-27-4 triethoxy(4-methoxyphenyl)silane 
• 1206544-10-6 4′-methoxy-3,4-dihydro-[1,1′-biphenyl]-1(2H)-ol 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 13139-86-1 4-methoxyphenyl magnesium bromide 
• 108-94-1 cyclohexanone 
• 5323-87-5 3-Ethoxycyclohex-2-en-1-one 
• 117360-96-0 3-<(1-methylpropyl)oxy>-2-cyclohexen-1-one 
• 15321-51-4 diiron nonacarbonyl 

Downstream Products

• 107203-08-7 3-(4-methoxyphenyl)cyclohexanone 
• 29097-92-5 3-(4-hydroxyphenyl)-2-cyclohexen-1-one 
• 60901-15-7 (+/-)-cis-3-(4-Methoxy-phenyl)-cyclohexanol 
• 101595-63-5 [4-(4-methoxy-phenyl)-2-oxo-cyclohex-3-enyl]-glyoxylic acid ethyl ester 
• 259662-70-9 (RS)-[3-(4-methoxy-phenyl)-cyclohex-2-enyl]-(3-phenyl-propyl)-amine 
• 259662-64-1 (RS)-[3-(4-methoxy-phenyl)-cyclohex-2-enyl]-phenethyl-amine 
• 1092571-57-7 (R)-3-(4-methoxyphenyl)-3-methylcyclohexan-1-one 
• 1251958-62-9 C₁₄H₁₈O₂ 
• 1199807-35-6 (S)-3-ethyl-3-(4-methoxyphenyl)cyclohexanone 
• 1251958-61-8 C₁₅H₂₀O₂ 
• 1415503-53-5 4-allyl-4'-methoxy-5,6-dihydro-[1,1'-bi(phenyl)]-3(4H)-one 
• 1415503-74-0 4-allyl-4'-methoxy-5,6-dihydro-[1,1'-bi(phenyl)]-3-yl 2-chloroacetate 
• 53059-28-2 4'-methoxy-[1,1'-biphenyl]-3-amine 
• 156334-43-9 C₁₃H₁₅NO₂ 

Relevant articles and documents

A practical route to arylated dihydroacridine derivatives via nickel boride mediated intramolecular reductive cyclization-concomitant dehydration

A facile and highly efficient route towards 3-aryl-1,2-dihydroacridine derivatives from an aldol adduct of o-nitrobenzaldehyde and cyclohexenone derivatives has been described. In situ generated nickel boride was found to be an excellent reagent to construct the acridine framework via an intramolecular reductive cyclization reaction at ambient temperature under acid-free conditions. The reaction is proved to be compatible from the milligram to multigram scale. Operational simplicity, good yields, a broad substrate scope, and scalability make this protocol a valuable addition to the existing methods for acridine derivatives.

Arene Trifunctionalization with Highly Fused Ring Systems through a Domino Aryne Nucleophilic and Diels–Alder Cascade

A convenient and efficient domino aryne process was developed under transition-metal-free conditions to generate a range of tetra- and pentacyclic ring systems. This transformation was realized via a 1,2-benzdiyne through a nucleophilic and Diels–Alder reaction cascade using styrene as the diene moiety. Three new chemical bonds, namely one C?N and two C?C bonds, and two benzofused rings could be constructed concomitantly, which was made possible by distinct chemoselective control at both the 1,2-aryne and 2,3-aryne stages. Moreover, in-depth studies were carried out on the domino aryne precursors and controlling the diastereoselectivity.

ANTICONVULSANT COMPOUNDS

The present application relates to compounds and methods for reducing the severity of convulsant activity or epileptic seizures, or for the treatment of chronic or acute pain.