127047-17-0

Basic information

• Product Name: 5-(4-methoxyphenyl)pentan-1-al
• Synonyms: 5-(4-methoxyphenyl)pentan-1-al
• CAS NO: 127047-17-0
• Molecular Weight: 192.258
• Mol File: 127047-17-0.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: 5-(4-methoxyphenyl)pentan-1-al(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(4-methoxyphenyl)pentan-1-al(127047-17-0)
• EPA Substance Registry System: 5-(4-methoxyphenyl)pentan-1-al(127047-17-0)

Safety Data

• Hazardous Substances Data: 127047-17-0(Hazardous Substances Data)

Upstream product

• 854401-87-9 1,10-bis-(4-methoxy-phenyl)-decane-5,6-diol 
• 546-67-8 lead(IV) tetraacetate 
• 71-43-2 benzene 
• 821-09-0 n-Pent-4-enyl alcohol 
• 696-62-8 para-iodoanisole 
• 52220-42-5 1-((E)-4-Chloro-but-2-enyl)-4-methoxy-benzene 
• 30448-78-3 p-methoxyphenylbutadiene 
• 201230-82-2 carbon monoxide 
• 140-67-0 Estragole 
• 101268-18-2 methyl 5-(4-methoxyphenyl)pentanoate 
• 123-11-5 4-methoxy-benzaldehyde 
• 344360-08-3 5-(4-methoxyphenyl)pent-2-enoic acid ethyl ester 
• 20401-88-1 3-(4-methoxyphenyl)propional 
• 5406-18-8 3-(p-methoxyphenyl)-1-propanol 

Relevant articles and documents

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Method for synthesizing fluorescent dye intermediate aldehyde by hydroformylation of 1,3-diene compound

The invention discloses a method for synthesizing a fluorescent dye intermediate aldehyde by hydroformylation of 1,3-diene compound. The method comprises the following steps: S1, sequentially adding 0.01 mmol (1 mol%) of [Rh(cod)Cl]2, 0.1 mmol of a phosphine ligand(P/Rh=10/1) and 1 mmol of diene into a reaction flask, adding 1 ml of a solvent DMF, putting the reaction flask into a high-pressure reaction kettle, after the reaction is finished, transferring a mixed solution into a 25 mL glass bottle with 200 microliters of n-tridecane as an internal standard by using a rubber head dropper, and detecting; and S2, determining the product yield and the structure through a gas chromatograph and a nuclear magnetic resonance spectrum, wherein the obtained olefin conversion rate is larger than 99%, the aldehyde yield ranges from 61% to 99%, and the regioselectivity of the product aldehyde ranges from 70/30 to 100/0. According to the method disclosed by the invention, the separation and purification steps of aldehyde products are simplified, and the substrate of the dialkene hydroformylation reaction is excellent in universality.

Rhodium-Catalyzed Remote C(sp3)?H Borylation of Silyl Enol Ethers

A rhodium-catalyzed remote C(sp3)?H borylation of silyl enol ethers (SEEs, E/Z mixtures) by alkene isomerization and hydroboration is reported. The reaction exhibits mild reaction conditions and excellent functional-group tolerance. This method is compatible with an array of SEEs, including linear and branched SEEs derived from aldehydes and ketones, and provides direct access to a broad range of structurally diverse 1,n-borylethers in excellent regioselectivities and good yields. These compounds are precursors to various valuable chemicals, such as 1,n-diols and aminoalcohols.

Synthesis, in vitro and in silico evaluation of diaryl heptanones as potential 5LOX enzyme inhibitors

A new series of diaryl heptanones (12a-q) were synthesized and their structures were confirmed by its 1H, 13C NMR and Mass spectral data. These analogs were evaluated for their anti-oxidant activity and potential to inhibit 5-lipoxygenase. Compounds 12k and 12o showed potent in vitro 5-lipoxygenase enzyme inhibitory activity with IC50 values of 22.2, 21.5 μM, which are comparable to curcumin (24.4 μM). Further they also have shown significant antioxidant activity. Molecular docking studies clearly showed correlation between binding energy and potency of these compounds.