28469-48-9

Basic information

• Product Name: 6-hydroxycyclohex-1-enecarbonitrile
• Synonyms: 6-hydroxycyclohex-1-enecarbonitrile
• CAS NO: 28469-48-9
• Molecular Weight: 123.155
• Mol File: 28469-48-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 6-hydroxycyclohex-1-enecarbonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 6-hydroxycyclohex-1-enecarbonitrile(28469-48-9)
• EPA Substance Registry System: 6-hydroxycyclohex-1-enecarbonitrile(28469-48-9)

Safety Data

• Hazardous Substances Data: 28469-48-9(Hazardous Substances Data)

Upstream product

• 764-59-0 hex-5-en-1-al 
• 2537-48-6 diethyl 1-cyanomethylphosphonate 
• 111-30-8 Glutaraldehyde 

Downstream Products

• 721449-61-2 6-(4-methoxyphenyl)-1-cyclohexene-1-carbonitrile 
• 129527-97-5 1,4,5,6-tetrahydro-[1,1'-biphenyl]-2-carbonitrile 
• 14210-94-7 2-Cyan-1,3-cyclohexadien 
• 2050-68-2 4,4'-dichlorobiphenyl 
• 581-80-6 4,4'-bis(trifluoromethyl)biphenyl 
• 613-33-2 (4,4'-dimethyl-1,1'-biphenyl) 
• 92-52-4 biphenyl 
• 130251-99-9 6-acetoxy-1-cyclohexene-1-carbonitrile 

Relevant articles and documents

Intramolecular Morita-Baylis-Hillman adducts via sequential MBH and ring-closing-metathesis reactions

Using a tandem Morita-Baylis-Hillman (MBH) and ring-closing-metathesis (RCM) sequence, an alternative high yielding method for the construction of intramolecular Morita-Baylis-Hillman (IMBH) mono- and bicyclic functionalized cycloalkenols is reported.

Development of aliphatic alcohols as nucleophiles for palladium-catalyzed DYKAT reactions: Total synthesis of (+)-hippospongic acid A

The ability to use aliphatic alcohols as competent nucleophiles in the palladium-catalyzed dynamic kinetic asymmetric transformation of Baylis-Hillman adducts is explored. High yield and enantioselectivity is obtained for both the kinetic transformation a

THE WITTIG-HORNER REACTION IN HETEROGENOUS MEDIA VIII. CYCLIZATION DURING THE ALDOLISATION STEP FROM AQUEOUS GLUTARALDEHYDE

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