Cetonas

2-Amino-7,8-dihydroquinazolin-5(6H)-one is a research chemical that belongs to the group of quinazolinones. It is a useful building block for the synthesis of other compounds. This compound can be reacted with various reagents to form new compounds. 2-Amino-7,8-dihydroquinazolin-5(6H)-one has been used as a starting material in the synthesis of PET imaging agents for diagnostic and therapeutic purposes. This compound is also used as a reaction component in organic chemistry research.

4-Aminopyridazin-3(2H)-one is an antiplatelet drug that has been shown to have a pharmacological effect on the central nervous system. It is also used as a chemotherapeutic agent for the treatment of certain types of cancer. 4-Aminopyridazin-3(2H)-one contains two nitrogen atoms that are substituted with methyl groups, which can be hydrolyzed by liver enzymes to form pyridazine and 4-aminopyridine. 4-Aminopyridazin-3(2H)-one inhibits bacterial growth by inhibiting protein synthesis and cell division at the ribosome level. This drug also has antimicrobial activity against Gram-positive bacteria and fungi, but is not active against Gram-negative bacteria such as Escherichia coli.

3-Fluoro-2-methylphenylacetone is a reaction component and reagent that is useful in the synthesis of complex compounds. 3-Fluoro-2-methylphenylacetone, also known as 2-fluoromethylbenzaldehyde, is a versatile building block that can be used to synthesize a wide variety of chemical compounds. It has been shown to be an excellent intermediate and building block for the synthesis of pharmaceuticals, pesticides, agrochemicals, specialty chemicals, and other organic compounds. 3-Fluoro-2-methylphenylacetone is a fine chemical that has CAS No. 1017060-34-2.

4,6-Dimethoxy-1H-1,3,5-triazin-2-one is a conjugate of pyridinium with an amide. The compound has been used as a disinfectant for surfaces and in the treatment of wounds. It is also used as a biocide in water treatment. This compound has shown to be effective against Staphylococcus aureus and other bacteria, as well as some fungi. 4,6-Dimethoxy-1H-1,3,5-triazin-2-one can be synthesized from 2-(4'-methoxyphenyl)acetonitrile and chloral hydrate. The compound contains functionalities such as amines and oligosaccharides that are important for its antimicrobial activity.

5-Pyridin-2-yl-1H-pyridin-2-one is a chemical compound that belongs to the group of reactive dyes. It is a stable process that can be used for coupling with methoxy groups. This product has been shown to be a stable, high yield chemical that can be used in industrial large scale production. It is also considered an environmentally safe chemical because it does not pollute the environment and has low toxicity. 5-Pyridin-2-yl-1H-pyridin-2-one undergoes bromination reactions and has been shown to have nucleophilic properties.

2,2,4-Trimethylcyclopentanone is a cyclic ketone with the molecular formula CH(CH)3CO. It has a tautomeric equilibrium with 2,2-dimethylcyclohexanone. The compound is prepared by the addition of acetyl chloride to an aldehyde in the presence of base. The compound exhibits UV absorption at 270 nm and an uv spectrum indicative of a cyclic ketone. The compound can be synthesized from 2-methylcyclohexanol and formaldehyde in the presence of potassium hydroxide or sodium hydroxide. 2,2,4-Trimethylcyclopentanone has been used as a synthetic intermediate for other cyclic ketones as well as for pharmaceuticals, flavoring agents, and fragrances.

5-Ethoxy-2(5H)-furanone is an oxidation product of 5-ethoxy-2(5H)-furanone. It has an isomeric, stereospecific, regiospecifically, and a tautomeric relationship with furfural. 5-Ethoxy-2(5H)-furanone can be produced by the oxidation of furfural with boron trifluoride etherate in the presence of iodosobenzene. The reaction mechanism involves the addition of hydrogen peroxide to the boron trifluoride etherate to form hydroperoxydiborane. This compound then reacts with iodosobenzene to produce 5-ethoxy-2(5H)-furanone and 2,5-dihydroxybenzaldehyde. The reaction produces a mixture of diastereomers that contain different numbers of carbon atoms due to the regiospecific

Iprodione is an ester hydrochloride that belongs to the class of fungicides. It has been shown to have high resistance and is used in vitro assays to detect mutants with a high degree of resistance. Iprodione inhibits the growth of wild-type strains, but not resistant mutants, by inhibiting protein synthesis at the ribosome level, blocking the polymerase chain reaction and DNA replication. This prevents transcription and replication of genetic material. Iprodione also inhibits nitrite ion production in wild-type strains and has genotoxic effects on cultured human cells. The drug is metabolized through a number of metabolic transformations, including hydrolysis by esterases or glucuronidases, oxidation by cytochrome P450 enzymes, reduction by glutathione reductase, or conjugation with glucuronic acid.

Boc-(3S)-3-amino-4-phenyl-2-butanone is a chemical intermediate that is useful as a building block in organic synthesis. It has been used as a reaction component, reagent and high quality research chemical. Boc-(3S)-3-amino-4-phenyl-2-butanone is also a versatile building block and useful intermediate for the preparation of complex compounds. This chemical has shown to have speciality applications in fine chemicals such as pharmaceuticals and agrochemicals.

3-Ethyl-4-methyl-3-pyrrolin-2-one is a sulfonated dione that can be synthesized from chloroformates. The product yields are high and the compound is stable to heat, light, and hydrolysis. The compound crystallizes in a single pure form and does not contain any impurities. 3-Ethyl-4-methyl-3-pyrrolin-2-one has been used as a precursor for the synthesis of various other organic compounds. It can also be used to synthesize dimers with an aryl group at the end of the molecule.