Building Blocks

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-Chloro-5-methylbenzonitrile belongs to the class of carboxylic arylboronic acids, which are used in the synthesis of amides, ketones, and esters. The transformation of 3-chloro-5-methylbenzonitrile can be achieved by nitriles or tetrazoles. Nitriles are converted into cyanation products by treatment with hydrogen cyanide (HCN). Tetrazole is converted into a heteroarene by treatment with sodium azide (NaN3). The resulting heteroarenes can react with an ester to produce a substituted benzene.</p>

<p>5-Methyl-2-(tributylstannyl)pyridine (MTBP) is a ligand that has been used to polymerize ethylene. It is synthesized by the hydrosilylation of 2-bromopyridine with tributyltin hydride, followed by reaction with trimethylaluminium in a cavity. MTBP has been shown to be an effective catalyst for the hydrosilylation of olefins, where it can be used as a replacement for bulky and expensive transition metals such as platinum. 5-Methyl-2-(tributylstannyl)pyridine can also be used to catalyze the synthesis of supramolecular structures and photophysical processes.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>5-(Difluoromethyl)furan-2-carboxylic acid (5FFA) is a metabolite of the nitrofurantoin antibiotic. It is an orally bioavailable diuretic that has significant enhancement of urinary excretion of water and electrolytes. 5FFA inhibits the activity of the sodium ion transporter, which is responsible for reabsorption of sodium ions in the kidney tubules, and thus increases the excretion rate of sodium ions. In addition, 5FFA inhibits the activity of the potassium ion transporter, and enhances potassium ion excretion. This drug has been shown to have a long-term inhibitory effect on urinary tract infections due to its ability to inhibit bacterial growth. The oral bioavailability of 5FFA is significantly enhanced by combining it with diuretics such as furosemide or ethacrynic acid.<br>5FFA targets bacterial DNA gyrase, topoisomerase IV, and human organic</p>

<p>2-Bromo-3-methyl-5-formylthiophene is a photovoltaic material that can be used in dye-sensitized solar cells. It absorbs light at wavelengths of 300 to 800 nanometers and has a high efficiency of more than 10%. The compound's photophysical properties are sensitive to irradiation, which may be a concern for its use in solar cells. The compound is made up of nanocrystalline thin films that are deposited on an acrylic acid substrate. This process can be done systematically to produce a large number of 2B3MTs.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>N-Methyl-6-nitropyridin-3-amine is a pyridine derivative that can stabilize the geometry and conformation of other molecules. It also has a high sensitivity to changes in the environment and is able to react with nitro groups. The nitro group is an electron donor, which stabilizes the nitro group's electrons. This makes it possible for NMPNA to be used as a crystallization agent or to analyze the structure of crystals. The molecule's crystal structure is composed of a pyridine ring with three nitro groups. A parametric analysis was conducted on the effects of different parameters on crystal structures and their diffraction patterns.</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>1,5-Dichloro-2-iodo-3-nitrobenzene is a molecule with a benzene ring and a nitro group. This compound has a dihedral angle of 180° and crystallizes as the orthorhombic system. The crystal structure contains molecules of 1,5-dichloro-2-iodo-3-nitrobenzene that are linked by sharing an edge or corner. The molecule has two chlorines located on the same side of the benzene ring, which gives it a double bond between these two atoms. One of the iodine atoms is located in the 5 position on the benzene ring, while the other is in the 3 position. The nitro group is in the 2 position on the benzene ring. This compound's molecular formula is C 6 H 4 Cl 2 I 2 N 2 O 2 .</p>

<p>N-(4-Aminophenyl)-3-methylbutanamide is a chloride ionophore that is used as an antimicrobial agent. It has been shown to be active against E. coli, Staphylococcus aureus, and Proteus mirabilis. The addition of N-(4-aminophenyl)-3-methylbutanamide to the growth medium leads to an increase in the number of protonated molecules on the surface of bacterial cells. This increased proton concentration increases the permeability of bacteria to chloride ions and other halides, thereby causing cell death by osmotic lysis. The activity of this compound is also enhanced by magnetic fields and fluconazole or sulphonamides.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>2-Bromo-5-[(Z)-2-bromo-2-nitroethenyl]furan is a new antibiotic that has been shown to be effective against Staphylococcus aureus and other organisms. The mechanism of action is not yet known, but it seems to work by binding to DNA, preventing transcription and replication. It has been shown to induce necrosis in S. aureus and other bacteria, which may be due to its ability to induce the production of proinflammatory cytokines such as TNFα and IL-1β in vitro. This drug also has cytotoxic effects on human cells and may have the potential for use as an anticancer agent.<br>!-- END OF DESCRIPTION --&gt;</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1-Ethynyl-4-isocyanatobenzene is a compound that is used in spectroelectrochemistry. It is a nonpolar, electron donor and has a radical cation that can dimerize. This chemical has functionalities such as osmium and ligands. 1-Ethynyl-4-isocyanatobenzene can reversibly transfer an electron to ruthenium, which then oxidizes the solvent. The solvent may then be removed by solvents such as ether or tetrahydrofuran.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>