Building Blocks

Versatile small molecule scaffold

2-Chloro-6-methoxyquinoline-3-methanol is a supramolecular compound that is made up of a quinoline derivative and an alcohol. It has two isomers, which can be distinguished by observing their reaction time. The synthesis of 2-chloro-6-methoxyquinoline-3-methanol begins with the reaction of synthons and zinc oxide nanoparticles. This reaction produces a helical structure, which is then heated to produce acrylonitrile. The final step in the synthesis of 2CQM is the dehydration of the acrylonitrile using hydrogen bond interactions and heat to give 2CQM. Crystal x-ray diffraction studies have shown that 2CQM has a conformational skeletal structure with a ZnO core surrounded by four chloride ions and six methoxy groups on each side.

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

4H,5H-[1,2,4]Triazolo[4,3-a]quinazolin-5-one is a quinazolinone drug that inhibits bacterial growth by binding to the DNA gyrase enzyme. It is active against Gram-positive and Gram-negative bacteria. 4H,5H-[1,2,4]Triazolo[4,3-a]quinazolin-5-one has been shown to have broad antimicrobial activity against both aerobic and anaerobic organisms. This compound also has a low toxicity to mammalian cells in culture. The mechanism of action of this drug is not fully understood but may be related to its ability to inhibit cell growth by interfering with protein synthesis or cell division.

Versatile small molecule scaffold

1-(4-Fluorophenyl)-3-methylbut-2-en-1-one is a conformationally constrained analogue of diethyl malonate. It is an analog of diethyl malonate that has been stabilized by the addition of a fluorine atom in the para position. This molecule has three chiral centers, and its crystal structure has been determined using X-ray crystallography. The molecule has a planar surface with one hydroxyl group and one methyl group on each side of the plane. The molecule can be used as a fingerprinting probe and as an intermediate for organic synthesis.

Versatile small molecule scaffold

4-Cyclopropyl-6-methylpyrimidin-2-amine is a nitrogenous compound that can be taken up by plants through their roots and transported to other parts of the plant. It is used as a fungicide and is labelled for use on anaerobic soils, which are not suitable for many agricultural purposes. The uptake of 4-cyclopropyl-6-methylpyrimidin-2-amine has been shown to be initially high in the presence of oxygen, but decreases with time. It is also radioactive, emitting γ rays at a rate of 0.0003% per hour. 4-Cyclopropyl-6-methylpyrimidin-2-amine reacts with cyprodinil to form a pyrimidine intermediate, which then reacts with oxygen to form a final product that can be detected by radioactivity. In addition, this molecule has been found to have antiinflammatory effects in mice.

3-Methoxy-4-nitrobenzamide is an intermediate in the synthesis of drugs, dyes, and other organic chemicals. It is produced by the reaction of methoxyacetic acid with nitric acid. This compound is used as a starting material for the production of many pharmaceuticals, such as 3-methoxy-4-(2-chlorophenyl)benzamide, 3-methoxy-4-(2,6-dichlorophenyl)benzamide, and 3-methoxy-4-(3,4,5-trimethoxyphenyl)benzamide. 3MMB can also be used to synthesize acrylonitrile.

Geosmin is a volatile organic compound that is produced by certain types of bacteria, such as actinomycetes, and can be found in soil, water, and air. Geosmin has been identified as the cause of "earthy" or "musty" flavors in drinking water. Geosmin can be detected by olfactometry techniques and quantified using gas chromatography-mass spectrometry (GC-MS). The technique involves spiking a sample with an appropriate amount of geosmin to achieve the desired concentration for analysis. Geosmin can also be removed from samples using desorption methods. This process involves heating the sample at a high temperature to release geosmin from the surface adsorbed on the solid phase into the vapor phase where it can be collected on a trap. This method is used to analyze geosmin levels in environmental samples such as groundwater or surface water.