42052-30-2

Basic information

• Product Name: 2-Cyclononen-1-one, (2Z)-
• CAS NO: 42052-30-2
• Molecular Formula: C9H14O
• Molecular Weight: 138.21
• Mol File: 42052-30-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-Cyclononen-1-one, (2Z)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Cyclononen-1-one, (2Z)-(42052-30-2)
• EPA Substance Registry System: 2-Cyclononen-1-one, (2Z)-(42052-30-2)

Safety Data

• Hazardous Substances Data: 42052-30-2(Hazardous Substances Data)

Upstream product

• 74173-14-1 1-Trimethylsilyloxy-1-cyclononen 

Downstream Products

• 72357-98-3 cyclonon-2-en-1-one tosylhydrazone 
• 10060-20-5 (Z)-3-cyclodecen-1-one 
• 10035-96-8 trans-Cyclodec-3-en-1-on 
• 540-08-9 heptadecan-9-one 
• 462-18-0 tridecan-7-one 
• 120571-67-7 3-(2-Oxo-2-phenylethyl)cyclononanone 
• 98-86-2 acetophenone 
• 120571-65-5 6-phenyl-⁽⁶⁾(2,4)pyridinophane 
• 352304-41-7 butylcycloheptylprodigiosin 
• 124267-78-3 3-Methylcyclonon-2-en-1-one tosylhydrazone 
• 62221-44-7 1,5-dicyclohexyl-3-pentanone 

Relevant articles and documents

Sensitized Photooxygenation of Silyl Enol Ethers of Cyclic Ketones

α,β-Unsaturated and α-hydroxy ketones are accessible in prototropic ene-reactions with singlet oxygen by sensitized photooxygenation of cyclic silyl enol ethers and subsequent reduction and solvolysis.In a competing silatropic ene-reaction α-silyloxyketones are formed.Formation of different products depends on ring size, configuration and substitution.At C-6 chirally substituted 2-cyclohexenones are synthesized for the first time by sensitized photooxygenation of chiral silyl enol ethers of optically active starting ketones.