16538-85-5

Basic information

• Product Name: Cyclooctane, phenyl-
• CAS NO: 16538-85-5
• Molecular Formula: C14H20
• Molecular Weight: 188.313
• Mol File: 16538-85-5.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Cyclooctane, phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclooctane, phenyl-(16538-85-5)
• EPA Substance Registry System: Cyclooctane, phenyl-(16538-85-5)

Safety Data

• Hazardous Substances Data: 16538-85-5(Hazardous Substances Data)

Upstream product

• 14996-79-3 2-phenylcyclooctan-1-one 
• 4603-00-3 phenyl-cyclooctatetraene 
• 25328-90-9 1-phenylcyclooct-1-ene 
• 1552-12-1 1,5-cis,cis-cyclooctadiene 
• 100-56-1 phenylmercury(II) chloride 
• 7287-06-1 1-phenyl-1-cyclooctanol 
• 137407-47-7 (E)-1-phenylcyclooctene 
• 1556-09-8 cyclooctyl bromide 
• 368-47-8 phenyltrifluorosilane 
• 477773-51-6 cyclooctatetraene 
• 833-55-6 4-phenylheptanedinitrile 
• 931-88-4 1,2-cyclooctene 
• 71-43-2 benzene 
• 838-31-3 2-Cyan-1-amino-5-phenyl-cycloocten-⁽¹⁾ 

Downstream Products

• 82700-60-5 4-Cyclooctylbenzaldehyde 
• 137407-47-7 (E)-1-phenylcyclooctene 
• 1674-37-9 n-octanophenone 
• 171623-32-8 4-Cyclooctylacetophenone 
• 128309-63-7 4-Cyclooctyl-N,N-dimethyl-benzenesulfonamide 
• 128309-40-0 2-Cyclooctyl-N,N-dimethyl-benzenesulfonamide 
• 128309-54-6 3-Cyclooctyl-N,N-dimethyl-benzenesulfonamide 
• 187737-37-7 propene 
• 34557-54-5 methane 
• 74-85-1 ethene 
• 106-99-0 buta-1,3-diene 
• 95-13-6 1-indene 
• 71-43-2 benzene 
• 7287-06-1 1-phenyl-1-cyclooctanol 

Relevant articles and documents

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Indium Tribromide-Catalysed Transfer-Hydrogenation: Expanding the Scope of the Hydrogenation and of the Regiodivergent DH or HD Addition to Alkenes

The transfer-hydrogenation as well as the regioselective and regiodivergent addition of H?D from regiospecific deuterated dihydroaromatic compounds to a variety of 1,1-di- and trisubstituted alkenes was realised with InBr3 in dichloro(m)ethane. In comparison with the previously reported BF3?Et2O-catalysed process, electron-deficient aryl-substituents can be applied reliably and thereby several restrictions could be lifted, and new types of substrates could be transformed successfully in hydrodeuterogenation as well as deuterohydrogenation transfer-hydrogenation reactions.

Amino alcohols as ligands for nickel-catalyzed Suzuki reactions of unactivated alkyl halides, including secondary alkyl chlorides, with arylboronic acids

Suzuki cross-coupling reactions of an unprecedented array of unactivated primary and secondary alkyl halides (including challenging alkyl chlorides) can be accomplished through the use of nickel/amino alcohol-based catalysts. Both the nickel precatalyst and the amino alcohols (prolinol or trans-2-aminocyclohexanol) are commercially available and air-stable. In view of the remarkable diversity of amino alcohols that are readily accessible, this discovery may open the door to the rapid development of versatile catalysts for a wide range of cross-coupling processes. Copyright

Synthesis of Certain Mesogenic Azomethines Derived from 4-Cycloalkylanilines and from 4-Cycloalkylbenzaldehydes

General procedures are described for the synthesis of members of five pairs of related homologous series of mesogenic azomethines differing in the mode of linkage of the CH=N group and containing a cycloalkyl group in a terminal position.