Building Blocks

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Please enquire for more information about 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone including the price, delivery time and more detailed product information at the technical inquiry form on this page

3,4-Dichlorosulfolane is a chemical compound that has been shown to have both carcinogenic and non-carcinogenic effects in animals. It is an anthropogenic gas with a high global warming potential. The rate of formation of 3,4-Dichlorosulfolane depends on the concentration of atmospheric ozone. This gas also has a role in the regulation of physiological functions and growth factors in plants. 3,4-Dichlorosulfolane can be detected by mass spectrometry and plasma, which are used for chemical analyses.

Versatile small molecule scaffold

Cycloheptane-1,2-dione is an organic solvent that has a hydroxyl group and a methyl ethyl group. It is used as a reaction medium in the preparation of dioxime from ketones. Cycloheptane-1,2-dione is also used as an inhibitor in the kinetic study of reactions because it can be removed by physical methods or by adding a chlorine atom to form a compound with a nitro group. Cycloheptane-1,2-dione is also used in diagnosis tests for inhibition of compounds that are damaging to dry weight or for which radiation enhances their activity. These inhibitory compounds can be identified using cycloheptane-1,2-dione as the reagent. Cycloheptane-1,2-dione can be synthesized in large quantities and at low cost by reacting chlorine gas with dimethylcyclohexanone.

Tetramethyl-1,3-cyclobutanediol is a diacid that can be used as a monomer for the production of polyesters. It has conformational properties that are different from other diols. Tetramethyl-1,3-cyclobutanediol is soluble in hydrochloric acid and reacts with coatings containing dibutyltin oxide to produce residues. This chemical also reacts with copper oxide, resulting in the formation of copper cyclohexanol and dibutyltin oxide. Tetramethyl-1,3-cyclobutanediol is able to react with carboxylic acids to form esters. This compound has been shown to be employed in the synthesis of polycarboxylic acids such as adipic acid and sebacic acid. Tetramethyl-1,3-cyclobutanediol has been used in the production of polyester resins by reacting with ethylene glycol and tere

Versatile small molecule scaffold

2-Azaadamantane is a naphthalene derivative that is used as a precursor for the synthesis of other compounds. It undergoes catalytic hydrocarboxylation with hydrogen peroxide and ammonia to form 2-hydroxyadamantane. 2-Azaadamantane can also be oxidized to form 2-azaadamantane hcl. It has been shown that this compound can be used as an alternative to germanium in raman spectroscopy studies. 2-Azaadamantane hcl has a catalytic activity for hydrocarbons and iodinated compounds at temperatures below 200°C and pressures below 1 bar.

N-Anilinocarbonylglycine is a synthetic, optical, ethyl ester of hydantoin. It is produced by the reaction of aniline and glyoxylic acid in the presence of acetic anhydride and pyridine. The compound undergoes hydrolysis when treated with alkaline hydroxide solution. The kinetics of the reaction can be studied using a hydroxide solution as the base catalyst. In addition, N-Anilinocarbonylglycine has been shown to have membrane-stabilizing properties which may be due to its monocarboxylic acid group. This compound also undergoes catalytic deuterium isotope exchange reactions with chlorine gas in chloroform solution at room temperature.

Benzothiazoles and benzoxazoles are two classes of heterocyclic compounds that can be used to synthesize other biologically active molecules. 2-Bromo-3-methyl-2-butene is a coupling product that can be used in the synthesis of benzothiazole and benzoxazole. 2-Bromo-3-methyl-2-butene is an environmentally friendly reactant that gives high yields with alkenyl and heteroaromatic bromides. In addition, it can produce trisubstituted products with bromides as the only reagent.

1-Phenyl-1,2,3,4-tetrahydronaphthalene is a hydroxylated aromatic hydrocarbon that is used as a monomer in polymerization reactions. It is used in the production of styrene, which is an important chemical for the manufacture of polymers. 1-Phenyl-1,2,3,4-tetrahydronaphthalene has been shown to be effective as a polymerization initiator and can be used in pharmaceutical formulations. This compound can also be used as a solvent for hydrocarbons such as benzene and toluene. The particle size of 1-phenyl-1,2,3,4-tetrahydronaphthalene dictates its processability in the manufacturing process. The smaller the particle size of 1-phenyl-1,2,3,4-tetrahydronaphthalene particles are processed at a slower rate than larger particles

2-Ethylsulfanyl-6-methyl-pyrimidin-4-ol is a nitrogen heterocycle that can be used as a research chemical. It has been shown to have tumor necrosis factor activity and 6-methyluracil, which is an adamantyl substituent. This compound may also be an activator of hydrocarbon exocyclic radicals.

3-Bromo-2-hydroxycyclopent-2-en-1-one is used as a cycloaddition and aldol reaction catalyst. It has been shown to produce the highest yields in both reactions, with excellent synlett yields of β-unsaturated aldehydes and cyclopentenones. 3-Bromo-2-hydroxycyclopent-2-en-1-one can be used for the synthesis of tetracyclic, dihydrofuran, and other compounds that contain functional groups. 3Bromo 2HCPE is also lithiated to produce an intermediate in the synthesis of pharmaceuticals.

3,4-Dichlorobenzoyl chloride is an organic compound that is used as a building block in the synthesis of other compounds. It reacts with amines to form benzamides. 3,4-Dichlorobenzoyl chloride is also used to synthesize 5-nitrosalicylic acid, which is used for the treatment of degenerative diseases. 3,4-Dichlorobenzoyl chloride has been shown to inhibit efflux pumps in bacteria and inflammatory diseases by interacting with ATP binding cassette transporters. This compound can also reversibly oxidize nitrogen atoms in an electron reduction reaction.