141184-48-7

Basic information

• Product Name: 1-(3-(CYCLOPENTYLOXY)-4-METHOXYPHENYL)ETHANONE
• Synonyms: 1-(3-(CYCLOPENTYLOXY)-4-METHOXYPHENYL)ETHANONE
• CAS NO: 141184-48-7
• Molecular Formula: C₁₄H₁₈O₃
• Molecular Weight: 234.29
• Mol File: 141184-48-7.mol
• Article Data: 10

Chemical Properties

• Melting Point: 127-129 °C(Solv: ethyl acetate (141-78-6))
• Boiling Point: 356.6±22.0 °C(Predicted)
• Appearance: /
• Density: 1.096±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1-(3-(CYCLOPENTYLOXY)-4-METHOXYPHENYL)ETHANONE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3-(CYCLOPENTYLOXY)-4-METHOXYPHENYL)ETHANONE(141184-48-7)
• EPA Substance Registry System: 1-(3-(CYCLOPENTYLOXY)-4-METHOXYPHENYL)ETHANONE(141184-48-7)

Safety Data

• Hazardous Substances Data: 141184-48-7(Hazardous Substances Data)

Usage

General Description

1-(3-(cyclopentyloxy)-4-methoxyphenyl)ethanone is a chemical compound with the molecular formula C14H18O3. It is a ketone derivative, with a cyclopentyloxy group attached to the phenyl ring. 1-(3-(CYCLOPENTYLOXY)-4-METHOXYPHENYL)ETHANONE is commonly used in organic synthesis and pharmaceutical research as a building block or intermediate in the production of various drugs and other organic compounds. Its specific properties and potential uses may vary depending on the context in which it is being employed, but its structure suggests it may have applications in the development of pharmaceuticals, agrochemicals, and other materials. Further research and experimentation are likely needed to fully understand and exploit the potential of this compound.

Upstream product

• 67387-76-2 3-cyclopentyloxy-4-methoxybenzylaldehyde 
• 141184-47-6 1-methoxy-2-cyclopentyloxy-4-(1-hydroxyethyl)benzene 
• 917-54-4 methyllithium 
• 144036-17-9 3-cyclopentyloxy-4-methoxy benzoic acid 
• 676-58-4 methylmagnesium chloride 
• 60-29-7 diethyl ether 
• 121-33-5 vanillin 
• 137-43-9 Cyclopentyl bromide 
• 621-59-0 isovanillin 

Downstream Products

• 180992-27-2 [[1-(3-Cyclopentyloxy-4-methoxyphenyl)-1-ethenyl]oxy]trimethylsilane 
• 141184-49-8 3-cyclopentyloxy-4-methoxyacetophenone oxime 
• 1334336-05-8 6-(3-(cyclopentyloxy)-4-methoxyphenyl)-3-phenyl-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine 
• 1334336-04-7 6-(3-(cyclopentyloxy)-4-methoxyphenyl)-3-p-tolyl-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine 
• 1334336-03-6 6-(3-(cyclopentyloxy)-4-methoxyphenyl)-3-(3-methoxyphenyl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine 
• 1172617-18-3 6-(3-(cyclopentyloxy)-4-methoxyphenyl)-3-(2-methoxyphenyl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine 

Relevant articles and documents

Design, synthesis, biological evaluation and structural characterization of novel GEBR library PDE4D inhibitors

Memory and cognitive functions depend on the cerebral levels of cyclic adenosine monophosphate (cAMP), which are regulated by the phosphodiesterase 4 (PDE4) family of enzymes. Selected rolipram-related PDE4 inhibitors, members of the GEBR library, have been shown to increase hippocampal cAMP levels, providing pro-cognitive benefits with a safe pharmacological profile. In a recent SAR investigation involving a subset of GEBR library compounds, we have demonstrated that, depending on length and flexibility, ligands can either adopt a twisted, an extended or a protruding conformation, the latter allowing the ligand to form stabilizing contacts with the regulatory domain of the enzyme. Here, based on those findings, we describe further chemical modifications of the protruding subset of GEBR library inhibitors and their effects on ligand conformation and potency. In particular, we demonstrate that the insertion of a methyl group in the flexible linker region connecting the catechol portion and the basic end of the molecules enhances the ability of the ligand to interact with both the catalytic and the regulatory domains of the enzyme.

INHIBITORS OF PHOSPHODIESTERASE TYPE-IV

The present invention relates to oxazine derivatives, which can be used as selective inhibitors of phosphodiesterase (PDE) type IV. Compounds disclosed herein can be useful in the treatment of CMS disorders, AIDS, asthma, arthritis, bronchitis, chronic ob

Co-catalyzed reductive cyclization of azido and cyano substituted α,β-unsaturated esters with NaBH4: enantioselective synthesis of (R)-baclofen and (R)-rolipram

Sodium borohydride in combination with a catalytic amount of CoCl2 has been found to be an excellent catalytic system in reductive cyclizations of suitably substituted azido and cyano groups of α,β-unsaturated esters to afford γ and δ-lactams in high yields. The process has been demonstrated for the enantioselective synthesis of (R)-baclofen, (R)-rolipram, and (R)-4-fluorophenylpiperidinone, a key intermediate for (-)-paroxetine.