Building Blocks

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

5,6-Dichloro-3-nitropyridin-2-amine is a potent antiviral agent that is active against a broad spectrum of viruses. It has been shown to have selectivity for intracellular viruses, such as cytomegalovirus and herpes simplex virus type 1, and high cytotoxicity. 5,6-Dichloro-3-nitropyridin-2-amine interferes with the function of viral RNA by binding to the enzyme ribonucleotide reductase. This inhibits the synthesis of viral DNA and RNA, thereby inhibiting viral replication and transcription. The drug has also been shown to be encapsidated, making it resistant to degradation by serum enzymes and the proteolytic enzymes found in the gastrointestinal tract.

Chroman-6-carboxylic acid is a hydroxamic acid that is used in the production of carboxylate emulsions. It is an active substance that has been shown to inhibit the growth of bacteria and fungi. Chroman-6-carboxylic acid has also been shown to be a strong oxidizing agent, which can generate hydrogen peroxide in alkaline media. This agent also has functional groups such as carboxylate, chloride, and carboxylic acid.

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

2-Bromohexane is an organic compound and a chemical building block. It is produced by the reaction of 1,3-dibromohexane with copper. 2-Bromohexane is used in the production of epoxides and other chemicals. The synthesis of 2-bromohexane starts with the addition of bromine to 1,3-dibromohexane followed by the addition of copper (II) chloride. This reaction produces 3-bromohexane as a byproduct which can be removed from the reaction mixture using a Dean–Stark trap. In this process, two moles of hydrogen are used to convert one mole of bromine into one mole of hydrogen bromide gas, which can be easily condensed into liquid form. The monoalkylation product 2-bromohexane reacts with an alkyl halide to produce a mixture containing two different alkyl halides. These

2-Bromo-3,3,3-trifluoro-1-propene is a chemical compound that has been synthesized in an asymmetric reaction. The reactant is bromopropane and the product is 2,2,2-trifluoropropene. The methylene group on the propene molecule is activated by the nucleophilic attack of a fluoride ion from hydrogen fluoride to form a cavity with a highly strained bond. The kinetic study of this reaction revealed that the activation energy for the reaction is 42 kJ/mol. Palladium-catalyzed coupling reactions are catalyzed by palladium and require nonpolar solvents such as toluene or dichloromethane. This type of reaction has been shown to be exothermic with an isolated yield of 1%.

2-Phenoxyaniline is a nitro compound that can be converted to the corresponding palladium complexes. It is an inhibitor of the acylation reaction, which is a type of chemical reaction in which an organic molecule reacts with an acid. The inhibition of this reaction has been shown to have an effect on heart disease, specifically by lowering cholesterol levels and reducing atherosclerosis. 2-Phenoxyaniline has also been shown to inhibit the activation energy for electron transfer reactions, making it useful as a catalyst in analytical methods. 2-Phenoxyaniline also undergoes vibrational spectroscopy when exposed to liquid chromatography and other analytical methods.

Trans-1,2-Dichloroethylene is a chlorinated hydrocarbon that is used in the production of polyvinyl chloride plastics. When ingested at dietary concentrations, trans-1,2-Dichloroethylene may cause liver damage and death in CD-1 mice. Trans-1,2-Dichloroethylene has been shown to react with nucleophilic substitutions and produce toxic reaction products. This chemical also causes polymerase chain reactions that can lead to cell death. The effective dose for this chemical is unknown because it has not been tested in clinical trials.

Ethyl 3-formyl-1H-pyrrole-2-carboxylate is a formyl compound with the molecular formula C8H8O3. It is a colorless liquid that has a strong odor. The compound can be obtained by the reaction of ethyl acetoacetate and pyrrole in the presence of aluminum chloride. The compound has been studied for its nuclear magnetic resonance (NMR) properties. It has two conformers, which are distinguished by their different chemical shifts, and this difference can be used to study coupling between the carbonyl group and other groups in the molecule.

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

2,2',4,4'-tetrahydroxybenzophenone is a hydroxylated benzophenone that has immunomodulatory effects. It binds to the receptor in the immune system and can cause an increase in cytokine production. 2,2',4,4'-tetrahydroxybenzophenone is cytotoxic and has significant toxicity in vitro. The molecule has been shown to disrupt mitochondrial membrane potential. This may be due to its ability to form hydrogen bonds with molecules on the mitochondrial membrane. 2,2',4,4'-tetrahydroxybenzophenone also modulates transcriptional regulation of genes involved in cell proliferation and apoptosis. The drug is detectable at low levels by mass spectrometry and is not known to have any toxicological effects.END>>

2-Acetylbenzoic acid is a functional molecule that contains an acetyl group. It can form hydrogen bonds with other molecules and has been shown to induce apoptosis in cells. The reaction products of 2-acetylbenzoic acid are malonic acid, acetylsalicylic acid, and 2-benzoylbenzoic acid. These three compounds are made by the addition of hydrogen or hydroxide to the molecule 2-acetylbenzoic acid. The molecule has two functional groups: a carbonyl group and an acetyl group. The chemical structure of this molecule can be seen in the figure below.
2-Acetylbenzoic Acid

Versatile small molecule scaffold

Isononyl alcohol is a polycarboxylic acid that has been used in the treatment of skin conditions, such as atopic dermatitis and psoriasis. It has been shown to penetrate the skin and stimulate the production of sebum. Isononyl alcohol is also used as a plasticizer for polyvinyl chloride (PVC) and other plastics, which increases their flexibility. This chemical also has a hydrophobic effect, which may be due to its hydroxyl group. The unsaturated alkyl chain on this chemical also makes it susceptible to oxidation by ozone in air and water vapor in air. Isononyl alcohol is metabolized by humans through conjugation with glucuronic acid or sulfate esters.

Versatile small molecule scaffold

Versatile small molecule scaffold

Please enquire for more information about H-Ser-Ala-Glu-Glu-Tyr-Glu-Tyr-Pro-Ser OH trifluoroacetate including the price, delivery time and more detailed product information at the technical inquiry form on this page