![2-[(2,4-dichlorophenyl)methylidene]-6-[(4-fluorobenzyl)oxy]-1-benzofuran-3(2H)-one](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fcas-image%2Fthumb-webp%2F10372-2-24-dichlorophenyl-methylidene-6-4-fluorobenzyl-oxy-1-benzofuran-3-2h-one.webp&w=3840&q=75)
CAS 7048-40-0: 2-[(2,4-dichlorophenyl)methylidene]-6-[(4-fluorobenzyl)oxy]-1-benzofuran-3(2H)-one
Formula:C22H13Cl2FO3
InChI:InChI=1/C22H13Cl2FO3/c23-15-4-3-14(19(24)10-15)9-21-22(26)18-8-7-17(11-20(18)28-21)27-12-13-1-5-16(25)6-2-13/h1-11H,12H2
SMILES:c1cc(ccc1COc1ccc2c(c1)OC(=Cc1ccc(cc1Cl)Cl)C2=O)F
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(2-methoxy-5-methylphenyl)methanol
CAS:(2-methoxy-5-methylphenyl)methanol is a compound that interacts with the 5-HT1A receptor, which is a subtype of serotonin receptor. It has been shown to have an affinity for the 5-HT1A receptor and can be used as a 5-HT1A receptor antagonist. The compound has been shown to inhibit adenylyl cyclase activity and also interact with this enzyme. (2-methoxy-5-methylphenyl)methanol has been shown to be an effective inhibitor of cyclic AMP production in membranes when used at high concentrations. This drug also inhibits the binding of 8-OHDPAT, a synthetic compound, to the 5HT1A receptor and can be used in assays to examine the effects of drugs on 5HT1A receptors. (2-methoxy-5-methylphenyl)methanol also binds selectively to membranes and inhibits cyclase activity.Formula:C9H12O2Purity:Min. 95%Molecular weight:152.19 g/mol(2-Methoxy-5-methylphenyl)methanol
CAS:Formula:C9H12O2Purity:98%Color and Shape:LiquidMolecular weight:152.19042-Methoxy-5-methylbenzyl alcohol
CAS:2-Methoxy-5-methylbenzyl alcoholPurity:95%Molecular weight:152.19g/mol