1228050-59-6

Basic information

• Product Name: C₁₇H₁₈
• Synonyms: C₁₇H₁₈
• CAS NO: 1228050-59-6
• Molecular Weight: 222.33
• Mol File: 1228050-59-6.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: C₁₇H₁₈(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₇H₁₈(1228050-59-6)
• EPA Substance Registry System: C₁₇H₁₈(1228050-59-6)

Safety Data

• Hazardous Substances Data: 1228050-59-6(Hazardous Substances Data)

Upstream product

• 77134-00-0 3-(4-methylphenyl)prop-2-enyl acetate 
• 5142-75-6 tri(p-tolyl)bismuth 
• 55-21-0 benzamide 
• 766-97-2 4-n-methylphenylacetylene 
• 624-31-7 4-tolyl iodide 
• 5720-05-8 4-methylphenylboronic acid 
• 104-09-6 4-methylphenylacetaldehyde 
• 699-02-5 4-Methylphenethyl alcohol 
• 166824-04-0 4-methyl-α-[(1E)-2-(4-methylphenyl)ethenyl]benzenemethanol 
• 122-00-9 para-methylacetophenone 
• 104-87-0 4-methyl-benzaldehyde 
• 13565-37-2 trans-4,4'-dimethylchalcone 
• 13677-51-5 1,3-bis(4-methylphenyl)prop-2-en-1-ol 

Downstream Products

• 942029-54-1 2,4-di-p-tolyl-4H,5H-pyrano[3,2-c]chromen-5-one 
• 1235117-69-7 4,4'-((1E,4E)-5-chloro-5-phenylpenta-1,4-diene-1,3-diyl)bis(methylbenzene) 
• 1356470-27-3 (E)-N,3-di-p-tolylacrylamide 
• 87797-64-6 6-methyl-2,4-di-(p-tolyl)quinoline 

Relevant articles and documents

Deoxygenative coupling of 2-aryl-ethanols catalyzed by unsymmetrical pyrazolyl-pyridinyl-triazole ruthenium

A pyrazolyl-pyridinyl-triazole Ru complex was synthesized from unsymmetrical pyrazolyl-pyridinyl-triazole (PPT) skeleton ligand and characterized through X-ray crystallography. The corresponding heterogeneous pyrazolyl-pyridinyl-triazole Ru complexes on γ

Oxygenation of Simple Olefins through Selective Allylic C?C Bond Cleavage: A Direct Approach to Cinnamyl Aldehydes

A novel metal-free allylic C?C σ-bond cleavage of simple olefins to give valuable cinnamyl aldehydes is reported. 1,2-Aryl or alkyl migration through allylic C?C bond cleavage occurs in this transformation, which is assisted by an alkyl azide reagent. This method enables O-atom incorporation into simple unfunctionalized olefins to construct cinnamyl aldehydes. The reaction features simple hydrocarbon substrates, metal-free conditions, and high regio- and stereoselectivity.

FeCl3·6H2O-catalyzed selective reduction of allylic halides to alkenes with concomitant oxidation of benzylic alcohols to aldehydes

Iron-catalyzed direct reduction of allylic halides with benzylic alcohol was achieved, providing a new, simple, and efficient method for conducting highly regioselective hydrodehalogenation. This method not only features a readily available reductant, an