Building Blocks

1-Chloroisoquinolin-4-ol is a phenylpyrimidine with anti-inflammatory properties. It is used in the treatment of sensitivity and mediated diseases, such as osteoarthritis, rheumatoid arthritis, and ankylosing spondylitis. 1-Chloroisoquinolin-4-ol inhibits the enzymatic activity of matrix metalloproteinases (MMPs), which are enzymes that break down collagen and other proteins in the body. The inhibition of MMPs by 1-chloroisoquinolin-4-ol leads to reduced inflammation and pain. This compound is also an effective inhibitor of the activities of chloride channels involved in acid secretion by cells in the stomach lining, thus inhibiting acid production. 1-Chloroisoquinolin-4-ol has been shown to have anticholesterolemic effects on liver cells due to its ability to inhibit cholesterol synthesis through inhibition of HMG CoA

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

N-(2-Phenylethyl)benzenesulfonamide is a biodegradable and aerobic catalyst that is used in the production of nitrates. It can be recycled and has a high solubility, which allows for efficient extraction from wastewater effluents. The reactor system can be operated at an aerobic or anaerobic conditions. N-(2-Phenylethyl)benzenesulfonamide is soluble in water and can be hydrolyzed by acids or bases to release ammonia gas. The process can also be sustainable due to the use of renewable energy sources such as solar, wind, tidal, or biomass power.

Versatile small molecule scaffold

Versatile small molecule scaffold

Rac-2,2'-Methylenebis(4-oxatricyclo[5.2.1.0,2,6]dec-8-ene)-3,5-dione is a polyvalent anhydride that has been used as a crosslinking agent in epoxy resin systems and as a viscosity modifier in polymerizable systems. It is also used as an additive to improve the properties of powder coatings and to produce polycarboxylic acid dispersions for use in alkyd resins and oil field chemical additives. The material is supplied as a colloidal suspension in water with a particle size of less than 1 micron. Racemic 2,2'-Methylenebis(4-oxatricyclo[5.2.1.0,2,6]dec-8-ene)-3,5-dione (rac-(1R,2S,6R,7S)-

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

2-Methylbenzene-1,3-dicarbaldehyde is a divalent hydrocarbon that has an oxidation catalyst. This compound is used as an intermediate in the production of drugs and pharmaceuticals. It has been shown to have cardiovascular disorders, such as vasodilatation and hypotension. The mechanism of action is not fully understood but may be related to its ability to act as a nitrovasodilator by increasing nitric oxide (NO) release. 2-Methylbenzene-1,3-dicarbaldehyde also produces psychotic disorders when long term exposure occurs. This compound has been shown to have neurotoxic effects in animal models with long term exposure.

4-Acetylmorpholine is a recycled amide that is synthesized from an alkanolamine and an acylation reaction. It has been used in the dehydrating of organic compounds, such as reaction solution, and for the preparation of acrylamide. 4-Acetylmorpholine is also used as a viscosity control agent in the extraction of aromatic hydrocarbons. Its chemical structure consists of a carbonyl group and an aromatic hydrocarbon. 4-Acetylmorpholine can be synthesized by reacting acetaldehyde with ammonia or thiourea with methyl chloride or ethylene oxide.

Dec-9-ynoic acid is a synthetic fatty acid that is a precursor to several biologically important substances. It is labile and easily oxidized by air, light, or heat. Dec-9-ynoic acid has been shown to be a central metabolic intermediate for the biosynthesis of polyunsaturated fatty acids. It can also be converted into linolenic acid, which is an essential fatty acid that cannot be synthesized by humans. Dec-9-ynoic acid exists in two geometric isomers: cis and trans. The cis form exhibits kinetic properties that are different from the trans form. Dec-9-ynoic acid has been studied as a potential treatment for human diseases such as diabetes mellitus type 2, Parkinson's disease, Alzheimer's disease, schizophrenia, and depression.

4-Hydroxy-2-naphthoic acid is a hydrocarbon with a carboxylic acid group. It can act as an antagonist to the hydrocarbon receptor (HCR). 4-Hydroxy-2-naphthoic acid has been shown to be effective in treating colon cancer cells in vitro, and has been shown to inhibit the growth of cancer cells in vivo. This compound is also effective at inhibiting the proliferation of human colon cancer cells (Caco2) that have been exposed to benzo(a)pyrene, an aromatic hydrocarbon found in cigarette smoke. The mechanism by which this drug inhibits cell proliferation is not fully understood but may involve inhibition of cytochrome P450 1A1 (CYP1A1), which metabolizes benzo(a)pyrene into carcinogenic intermediates. 4-Hydroxy-2-naphthoic acid has also been shown to be anisotropic and microreactor, meaning

3-Fluorobenzene-1-sulfonyl fluoride is a chemical compound that can be used as a catalyst to synthesize organic compounds. It is a colorless liquid, which is soluble in water and organic solvents. This catalyst has been shown to be more efficient than the traditional catalysts, such as tetraphenylphosphonium chloride, potassium fluoride or sodium borohydride. 3-Fluorobenzene-1-sulfonyl fluoride also reacts with nitro groups to produce dinitro compounds, which are valuable synthetic intermediates for the production of dyes and pharmaceuticals. The synthesis of this compound can be carried out in high yields with stoichiometric amounts of reactants.

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

(3,3,3-Trifluoroprop-1-yn-1-yl)benzene is a reaction product that can be used to inhibit the activity of metalloprotease and as an anti-cancer agent. This compound inhibits the enzyme that causes chronic kidney disease and degenerative diseases. It is a potent inhibitor of metalloprotease, which is involved in cancer progression, fatty acid synthesis and bone formation. The effective dose for this drug is between 1 and 10mg/kg body weight. It has been shown to have an asymmetric synthesis with the use of amido groups. (3,3,3-Trifluoroprop-1-yn-1-yl)benzene also has antirheumatic properties due to its ability to inhibit proteases such as matrix metalloproteinases and cathepsins.

Research has shown that (4-Ethoxy-3-methoxybenzyl)amine (EMBA) is a potent inhibitor of bacterial growth. The alkylation of EMBA with methylamine and benzene leads to the formation of aureus, which is an antibiotic that can be used to treat staphylococcus infections. In addition, EMBA can also be methylated with hydroxylamine to form benzylamine, a compound that inhibits the synthesis of the cell wall in bacteria. These properties make EMBA an effective antimicrobial agent.

Versatile small molecule scaffold

(S)-(+)-1-Bromo-2-methylbutane is a chiral molecule with two stereoisomers, the cis and trans forms. The cis form has been observed to be the more stable of the two. It is a functional theory that these two forms are not mirror images of each other because they have different conformations. (S)-(+)-1-Bromo-2-methylbutane has been used in the synthesis of a number of important molecules. The stereoisomers can be distinguished by conformational analysis and optical microscopy. (S)-(+)-1-Bromo-2-methylbutane also has an application in biotechnology for use as a precursor for hydrazones, which are important in organic chemistry and molecular biology, such as DNA sequencing.

Versatile small molecule scaffold

Versatile small molecule scaffold

Ethyl 5-oxoheptanoate is a clear, colorless liquid that can be synthesized by reacting benzene with acetone. The synthesis of ethyl 5-oxoheptanoate is an example of a Friedel-Crafts reaction. This chemical is soluble in organic solvents such as acetone and cyclohexane and has low toxicity. It can be used as a reagent for the preparation of esters from alcohols, phenols, or carboxylic acids. Ethyl 5-oxoheptanoate can also be used to prepare resorcinol, which is a precursor to polymers and dyes, by hydrogenation of the molecule. Preparative methods are often used to produce this product because it has limited solubility in water.

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

4'-(Methylsulfonyl)acetanilide is an organic compound that has been shown to have antibacterial and antiviral activity. It targets the benzene nucleus, and inhibits the synthesis of nucleic acids by inhibiting the enzyme ribonucleotide reductase. 4'-(Methylsulfonyl)acetanilide also inhibits viral replication, by binding to the active site of a viral protein (a DNA polymerase), which blocks the incorporation of nucleotides into the virus's DNA. In addition, 4'-(methylsulfonyl)acetanilide is an anti-helminthic agent, as it can inhibit worm motility and kill larvae in vitro. The structure-activity relationships between this molecule and other benzimidazole derivatives were analysed in order to identify new potential drugs for treating diseases caused by viruses or parasites.

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

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%.

1-Hydroxycyclopentane-1-carbonitrile is a monomer that is hydrolyzed to form benzoin and cyanohydrins. It can be used in the production of scifinder as a monomer or dimerizer.

3-Hydroxy-5-methylpyridine (3HMP) is a chemical substance that has been classified as an amine. It is a product of the metabolism of purines, which are nitrogenous bases found in DNA and RNA. 3HMP is produced by aerogenic bacteria (such as Enterobacter), and can be used to estimate the number of these bacteria present in water samples. 3HMP has been shown to have antiviral properties against influenza virus, and can be used as a biomarker for the presence of other viruses in animals. 3HMP also has mineralization properties, which have been studied extensively, particularly with regards to pancreatic disease.

Please enquire for more information about 4,5-Dihydro-1H-imidazol-2-amine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

Versatile small molecule scaffold

4,5-Dihydroxy-2,3-pentanedione is a carbonyl compound that is the product of the oxidation of ascorbic acid. It is used in wastewater treatment and has antimicrobial properties against infectious diseases. This compound has been shown to inhibit protein synthesis by binding to the ribosome and preventing the formation of peptide bonds between amino acids. 4,5-Dihydroxy-2,3-pentanedione has also been shown to bind to plasma proteins, which may be due to its acyl chain structure. 4,5-Dihydroxy-2,3-pentanedione can be synthesized in a catalytic mechanism that involves dehydroascorbic acid and molecular oxygen.

Piperyline is an alkanoic acid that has shown to be effective against skin cancer. It also has antimicrobial properties, which may be due to its ability to bind metal ions and form polymeric compounds. Piperyline inhibits microbial growth by inhibiting the synthesis of proteins and nucleic acids. The antimicrobial activity is related to its cationic polymerization with hydroxyl groups, which forms a structure that can inhibit microbial enzymes and disrupt microbial cell membranes. This compound also interacts with the skin's natural lipids, making it difficult for microorganisms to attach and grow on the skin. Piperyline is synthesized in organic chemistry laboratories as an amide precursor of other pharmaceuticals such as penicillin.