Ketones

4-Methoxy-2,5-dimethyl-3(2H)-furanone is a natural product that is found in the essential oil of the leaves and bark of several species of trees. It has been shown to have hypoglycemic effects and may be useful for the treatment of diabetes. This compound is extracted from plant tissues using solid phase microextraction (SPME) and analyzed by NMR spectroscopy. The chemical structure of 4-methoxy-2,5-dimethyl-3(2H)-furanone has been determined by gas chromatography/mass spectrometry (GC/MS). 4-Methoxy-2,5-dimethyl-3(2H)-furanone has also been shown to inhibit the growth of some cancer cells in tissue culture models. In addition, it can be used as a model protein for methyl anthranilate, which is an intermediate in the reaction pathway that produces this compound.

Please enquire for more information about (2Z)-6-Hydroxy-2-(4-methylbenzylidene)-1-benzofuran-3(2H)-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

2,2-Dimethyl-1,3-dioxolan-4-one is a dioxolane compound that can be used as a monomer in the polymerization of vinyl acetate with other vinyl compounds. It is also a ring-opening agent for the synthesis of methyl methacrylate from vinyl acetate and methacrylic anhydride. 2,2-Dimethyl-1,3-dioxolan-4-one copolymerizes with amines to form polymers. It can also be used to prepare styrene copolymers by reacting it with styrene and chlorobenzene.

3,8-Dihydroxy-6H-benzo[c]chromen-6-one (3,8 DHC) is a natural compound that has been shown to have antioxidant and anti-inflammatory properties. It increases the production of ATP (cellular energy) by activating the ATP binding cassette transporter and increasing autophagy. 3,8 DHC may also inhibit apoptosis (cell death), which has been observed in studies involving balloon injury and atherosclerotic lesions. This compound may also have potential therapeutic benefits for bowel disease, cancer, and neuronal death.

6alpha-Fluoro-11beta,17,21-Trihydroxypregna-1,4-Diene-3,20-Dione 17-Valerate is a hydrogenated and esterified form of 6alpha-fluoro-11beta,17,21-trihydroxypregna1,4diene3,20dione. It is an oil with a fatty acid ester that has been synthetically modified to be more hydrophobic. 6alpha-Fluoro-11beta,17,21-Trihydroxypregna1,4diene3,20dione 17valerate is used in the synthesis of pharmaceuticals and hormones. It can also be used as an enhancer for the stability of pharmaceutical preparations.

Please enquire for more information about 3-(4-Piperidinyl)-1,3-benzoxazol-2(3H)-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 5-(4-Butoxyphenyl)-1-(3,4-dimethylphenyl)-3-[(3,4-dimethylphenyl)amino]-1,5-dihydro-2H-pyrrol-2-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

Clascoterone is a topical antiandrogen, which is a synthetic steroidal product with mechanisms focused on inhibiting androgen receptors. Derived from a modified steroid structure, this compound exhibits a targeted approach to addressing conditions influenced by androgen activity, particularly in cutaneous applications. The mode of action of Clascoterone involves competitive inhibition at the androgen receptor sites, thereby reducing the impact of dihydrotestosterone, which plays a significant role in the pathophysiology of acne. Clascoterone is primarily utilized in the treatment of acne vulgaris. By decreasing sebum production and inflammatory responses mediated by androgens in the skin, it offers a non-systemic option for individuals experiencing this dermatological condition. The topical application allows for direct action on affected areas, minimizing systemic absorption and potential side effects associated with oral antiandrogens. This makes it a promising alternative for patients seeking targeted therapy with fewer systemic implications. Overall, Clascoterone offers a novel approach to acne management through its unique mode of local androgen suppression.

1,2,6,7-Tetrahydro-8H-indeno[5,4-b]furan-8-one is a synthetic compound that is used in the synthesis of melatonin receptor ligands. The group of compounds are designed to be trackable by positron emission tomography (PET) and computed tomography (CT) imaging. This compound has been shown to undergo debromination and hydrogenolysis with raney nickel to give 1,2-dibromoethane. Friedel-Crafts acylation produces tert-butyl 2-(1,2,6,7-tetrahydro-8H-[5′]-indeno[5′′]furan)-8-carboxylate after catalytic reduction. The elimination of tert butyl 2-(1,2,6,7-tetrahydro-8H-[5′]-indeno[5′′]fur

5-Nonanone is a fatty acid that has been shown to have significant interactions with hydrogen fluoride. It reacts with a hydroxyl group to form an ester and hydrogen fluoride, which may be due to the presence of a reactive methylene group. 5-Nonanone can also react with methyl ethyl or methyl pentanoate in the presence of hydrochloric acid, forming particle or phase transition temperature. The acute toxicity of 5-nonanone is low and there are no known chronic exposure effects.

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Please enquire for more information about (5E)-2-Mercapto-5-(3-methoxybenzylidene)-1,3-thiazol-4(5H)-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about (5-Amino-2-butylbenzofuran-3-yl)(4-(3-(dibutylamino)propoxy)phenyl)methanone oxalate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 1-[1-(2-Aminoethyl)-1H-indol-3-yl]ethanone oxalate including the price, delivery time and more detailed product information at the technical inquiry form on this page

2,6-Dimethyl-4H-pyran-4-one is a monosubstituted carbonyl compound that has hydrogen bond and redox potential characteristics. It is a reactive species that can be reduced to the corresponding methylene and oxidized to the corresponding carboxylic acid. The 2,6-dimethylpyranone has been used in coordination chemistry to form metal complexes. This molecule can also react with hydrochloric acid to form 2,6-dimethylhydrochloric acid or with sodium hydroxide to form 2,6-dimethylacetate. 2,6-Dimethylpyranone is typically used as an organic solvent in the production of fatty acids due to its ability to dissolve oils. It can also be used as a reagent in optical experiments due to its fluorescent properties.

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