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

2-Chloro-4-[(methylamino)methyl]pyridine

2-Chloro-4-(trifluoromethyl)quinoline is a polymer film that can be processed and has a high quantum efficiency. It has been shown to have efficient nonradiative energy transfer, which is due to the vibrational coupling between the polymer films. 2-Chloro-4-(trifluoromethyl)quinoline also has an efficient photophysical process and can be used in devices as a luminophore. The unoptimized theory of this material suggests that there are efficiencies in the range of 7%.

4-Chloro-6-fluoro-2-(trifluoromethyl)quinoline

Versatile small molecule scaffold

Versatile small molecule scaffold

2-Bromo-1-phenylbutan-1-one is a copper salt that yields an acceptor in the presence of acetonitrile. It is used as a diagnostic agent, yielding a blue color when reacted with diazonium salt. 2-Bromo-1-phenylbutan-1-one also reacts with dopamine to form the diagnostic dye 2,6 dibromopurpurin. This compound has been shown to be cytotoxic for mammary cancer cells and other cancer cells, but not for healthy cells. The mechanism of action of this compound may involve sulfate and copper ions, which are required for its activity.

2,3-Dimethoxybenzeneethanamine is a drug substance that belongs to the class of amines. It has been shown to have proarrhythmic effects in animal studies, and has also shown hypotensive properties. 2,3-Dimethoxybenzeneethanamine inhibits the binding of phenylephrine to adrenoceptors in rat heart tissue. This compound can be used as a chromatographic standard for dimethoxyphenethylamines and isomers due to its spectrometric properties.

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

2-Furan-2-yl-azepane

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

5-Chloro-3-methyl-1-(pyridin-2-yl)-1H-pyrazole-4-carbaldehyde is an organic compound that belongs to the class of substituted phenyl amides. It has a melting point of 187 degrees Celsius, and crystallizes in a centrosymmetric form. This substance reacts with nucleophiles through the hydrogen bonds present in its structure. The substituent on the phenyl group can be electron withdrawing or electron donating, which affects the reactivity. 5-Chloro-3-methyl-1-(pyridin-2-yl)-1H-pyrazole-4-carbaldehyde is useful for condensation reactions and can also form dimers that are stabilized by hydrogen bonding.

Versatile small molecule scaffold

Sodium 4-nitrobenzenesulfinate is a sulfonylating agent that is used in organic chemistry to synthesize dihydronaphthalene, which is an intermediate in the synthesis of naphthalenes. It can be prepared by the ring-opening reaction of sodium nitrobenzenesulfinate with a suitable nucleophile such as methylenecyclopropanes. Sodium 4-nitrobenzenesulfinate reacts with sulfur to form sulfones, which are important intermediates for the synthesis of thiazoles and benzothiazoles. This reagent has been shown to be effective for the synthesis of biomolecules, such as proteins and peptides.

Versatile small molecule scaffold

Methyl 2-methyl-3-sulfanylpropanoate is a fruity, tropical, and detergent scented ester with a fruity odor reminiscent of fruits. It is used in the manufacture of shampoo, as an acid methyl ester, or as an ethyl ester. This chemical has been used as a tobacco flavorant and can be found in the form of its methyl ester. Methyl 2-methyl-3-sulfanylpropanoate has been shown to have detergent properties when it is reacted with sodium hydroxide.

Versatile small molecule scaffold

4,4'-Bipyridine 1,1'-dioxide is a versatile compound used in various research applications. It has been found to have potential therapeutic effects in the treatment of certain diseases. This compound is commonly used as a ligand in coordination chemistry and has been studied for its ability to enhance the emission properties of other molecules. Additionally, 4,4'-Bipyridine 1,1'-dioxide has shown promise in the field of nuclear medicine as it can be labeled with positron or proton emitting isotopes for imaging purposes. Its unique structure and properties make it a valuable tool for scientists and researchers working in diverse fields such as pharmaceuticals, materials science, and biochemistry.

2-(4-Boc-piperazin-1yl)methylphenylboronic acid, pinacol

2,5-Dibromo-3-hex-1-ylthiophene

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

3-cyano-1H-indole-7-carboxylic acid is a potent, selective, and competitive inhibitor of the insulin receptor tyrosine kinase. It has been shown to be a more potent inhibitor of insulin receptor tyrosine kinase than insulin itself. 3-cyano-1H-indole-7-carboxylic acid binds to the ATP binding site on the receptor and blocks ATP binding, which prevents downstream signaling and leads to inhibition of cell proliferation. 3-cyano-1H-indole-7-carboxylic acid also inhibits the growth of cells in culture by altering cellular metabolism via inhibition of protein synthesis. The chemical structure of 3-(3'-cyanobiphenyl)-2-[(2'-propenyl)amino]-N-[4'-nitrobenzoyl]benzamide is similar to that of other known inhibitors such as piperazine and 2-(4'-nitro

Versatile small molecule scaffold

Versatile small molecule scaffold

4-Nitrophenylacetic acid is a chemical compound that belongs to the class of organic compounds known as nitrophenols. It has been shown to inhibit malonic enzyme, also known as 3-hydroxyacyl-CoA dehydrogenase. This inhibition is thought to be due to the nitro group on the molecule, which reacts with the active site cysteine residue in the enzyme. 4-Nitrophenylacetic acid can be used in the synthesis of monoclonal antibodies. The structure of 4-nitrophenylacetic acid has one hydroxyl group and two nitro groups that are separated by a methylene bridge (a carbon atom with two hydrogen atoms). The reaction solution for this substance contains diazonium salt and hydrochloric acid.

Versatile small molecule scaffold

3-Cyclopentyl-propionic acid amide is an organic compound that belongs to the group of monosubstituted, activating, dehydrating, nitrogen-containing compounds. It has medicinal properties and is used as a buffer for potassium ion in solution. 3-Cyclopentyl-propionic acid amide is also used in organic chemistry as a reagent for the synthesis of heteroaromatic rings. This compound binds to ion channels that are responsible for the initiation and conduction of impulses across nerve cells and helps eliminate both potassium ions and chloride ions from nerve cells. The connecting nitrogen atoms play a significant role in this process.

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

5-Hydroxymethyl-2'-deoxyuridine

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

7-Bromo-8-(trifluoromethyl)-1H-3,1-benzoxazine-2,4-dione

Versatile small molecule scaffold

2-(5-Bromopyridine-2-yl)-3-chloropyridine

Versatile small molecule scaffold

Versatile small molecule scaffold

Applications bis(2-Chloroethoxy)-d8-methane (cas# 93966-78-0) is a useful research chemical.

Versatile small molecule scaffold

Versatile small molecule scaffold

2,4-Dihydroxy-6-pentylbenzoic acid is a cannabinoid derivative. It is an enzyme that catalyzes the conversion of geranyl pyrophosphate to olivetolic acid. 2,4-Dihydroxy-6-pentylbenzoic acid has been shown to be a potent inhibitor of the activity of enzymes in the biosynthesis of olivetolic acid. This compound has been characterized as an inhibitor of olivetolic acid synthase and protein kinases. In vivo studies have shown that 2,4-dihydroxy-6-pentylbenzoic acid inhibits protein synthesis and induces apoptosis in some cancer cells by inhibiting protein synthesis and activating caspases.

Versatile small molecule scaffold

(5-Chloro-2-methoxy-4-pyridyl)boronic acid

Glutaric acid monoethyl ester chloride is an acid that has been used in pharmaceutical preparations and as a topical agent. It is used to treat chronic pulmonary diseases, such as asthma. The acidic properties of glutaric acid monoethyl ester chloride make it an effective agent for the treatment of autoimmune diseases, such as rheumatoid arthritis and multiple sclerosis. Glutaric acid monoethyl ester chloride also has dopamine-enhancing effects and can be used for the treatment of cancer. It is a monoclonal antibody that binds to brain infarction sites, preventing the progression of this disease. Glutaric acid monoethyl ester chloride has also been shown to have anti-inflammatory properties in bowel disease models, making it an effective treatment for inflammatory bowel disease (IBD).

2,2,6,6-Tetramethylcyclohexan-1-one is a chemical compound with the molecular formula CHO. It is a colorless liquid that boils around 100°C and has a strong odor. 2,2,6,6-Tetramethylcyclohexan-1-one can be used in the dehydrogenation of alicyclic compounds to form alkenes. The reaction proceeds by attack of the intermediate on the double bond and elimination of two hydrogen atoms from an adjacent methyl group. In this process, one molecule of water is also produced. This reaction mechanism can be postulated for homologues as well.