365553-73-7

Basic information

• Product Name: 1,4-Dioxaspiro[4.5]decan-8-ol, 8-(3-methoxyphenyl)-
• CAS NO: 365553-73-7
• Molecular Formula: C15H20O4
• Molecular Weight: 264.321
• Mol File: 365553-73-7.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: 1,4-Dioxaspiro[4.5]decan-8-ol, 8-(3-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-Dioxaspiro[4.5]decan-8-ol, 8-(3-methoxyphenyl)-(365553-73-7)
• EPA Substance Registry System: 1,4-Dioxaspiro[4.5]decan-8-ol, 8-(3-methoxyphenyl)-(365553-73-7)

Safety Data

• Hazardous Substances Data: 365553-73-7(Hazardous Substances Data)

Upstream product

• 4746-97-8 cyclohexanedione monoethylene ketal 
• 2398-37-0 3-methoxyphenyl bromide 
• 36282-40-3 (3-methoxyphenyl)magnesium bromide 

Downstream Products

• 40503-16-0 4-hydroxy-4-(3-methoxy-phenyl)-cyclohexanone 
• 147678-65-7 8-(3-methoxyphenyl)-1,4-dioxaspiro[4.5]dec-7-ene 
• 365553-76-0 8-(3-methoxyphenyl)-1,4-dioxaspiro[4.5]decane 
• 868142-19-2 8-(3-methoxy-phenyl)-1,3-diaza-spiro[4.5]decane-2,4-dione 
• 868142-49-8 8-(3-methoxy-phenyl)-2,4-dioxo-1,3-diaza-spiro[4.5]decane-1,3-dicarboxylic acid di-tert-butyl ester 
• 40503-91-1 4-(3-methoxyphenyl)cyclohexan-1-one 
• 147678-66-8 C₁₃H₁₄O₂ 
• 1297474-30-6 C₁₆H₁₈N₂O₂S 
• 1297474-39-5 C₁₆H₁₄N₂O₂S 
• 1297474-48-6 C₂₈H₂₄N₂O₆S 
• 1297474-14-6 C₂₆H₂₀N₂O₆S 
• 1402080-49-2 5-(3-methoxyphenyl)oxepan-2-one 

Relevant articles and documents

Desymmetrizing Isomerization of Alkene via Thiazolinyl Iminoquinoline Cobalt Catalysis

We report a cobalt-catalyzed desymmetrizing isomerization of exo-cyclic alkenes to generate chiral 1-methylcyclohexene derivatives with good yields and enantioselectivities. A novel chiral thiazolinyl iminoquinoline ligand and its cobalt complex were desi

Optimization of TRPV6 calcium channel inhibitors using a 3D ligand-based virtual screening method

Herein, we report the discovery of the first potent and selective inhibitor of TRPV6, a calcium channel overexpressed in breast and prostate cancer, and its use to test the effect of blocking TRPV6-mediated Ca2+-influx on cell growth. The inhib

Enantioselective baeyer-villiger oxidation: Desymmetrization of meso cyclic ketones and kinetic resolution of racemic 2-arylcyclohexanones

Catalytic enantioselective Baeyer-Villiger (BV) oxidations of racemic and meso cyclic ketones were achieved in the presence of chiral N,N'-dioxide-Sc III complex catalysts. The BV oxidations of prochiral cyclohexanones and cyclobutanones afforded series of optically active μ- and γ-lactones, respectively, in up to 99% yield and 95% ee. Meanwhile, the kinetic resolution of racemic 2-arylcyclohexanones was also realized via an abnormal BV oxidation. Enantioenriched 3-aryloxepan-2-ones, whose formation is counter to the migratory aptitude, were obtained preferentially. Both the lactones and the unreacted ketones were obtained with high ee values.