Building Blocks

<p>1-Amino-2-methylnaphthalene Hydrochloride is a crystalline solid that belongs to the class of supramolecular assembly. Crystals are colorless and have a melting point of 183 °C. It is soluble in ether, acetone, and other solvents. 1-Amino-2-methylnaphthalene Hydrochloride may be used as an intermediate of other organic compounds.</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>

<p>Versatile small molecule scaffold</p>

<p>Perfluorophenyl methanesulfonate is an organic solvent. It is a colorless liquid that is soluble in water and in most organic solvents. The chemical formula for perfluorophenyl methanesulfonate is C6F5OCH3SO3Cl. This compound has the structural formula of CH2=C(O)CH2-CF3SO3Cl. Perfluorophenyl methanesulfonate can be used as a formylating agent to convert alcohols, amines, or carboxylic acids into their corresponding formates, amides, or acid chlorides. It can also be used as an additive to petroleum products to increase the boiling point of hydrocarbons by adding a formyl group to the hydrocarbon chain. Other uses include as a divalent hydrocarbon in alkynyl groups and alkoxycarbonyl groups and as a skeleton for phosphoryl groups.</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>2-Methyl-2-p-tolyl-propylamine (MPTP) is an aromatic compound that has been shown to have some biologic activity. MPTP was first synthesized in the lab of Dr. K.B. Sharpless and his team at Duke University in 1979, who were attempting to make an inhibitor for monoamine oxidase B (MAO-B). MAO-B is a type of enzyme that breaks down the neurotransmitter dopamine, which is involved in the regulation of movement and emotions. The synthesis of MPTP was abandoned when it was found that the compound was instead metabolized into a neurotoxin called 1-methyl-4-phenylpyridinium (MPP+), which caused Parkinson's disease in mice.<br>MPTP causes cell death by inhibiting mitochondrial complex I, which produces adenosine triphosphate (ATP) needed for cell function, leading to cell death through apoptosis or necrosis</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>3-[({[4-(Ethoxycarbonyl)phenyl]carbamoyl}methyl)sulfanyl]propanoic acid is a research tool that is used as an activator of various receptors, ligands, and ion channels. This compound binds to the ligand binding site of the receptor and causes activation by increasing the rate of ligand-receptor interactions. 3-[({[4-(Ethoxycarbonyl)phenyl]carbamoyl}methyl)sulfanyl]propanoic acid has been shown to inhibit protein synthesis in cells by inhibiting peptide bond formation.</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>2-Amino-5-(2-fluorophenyl)-4-methyl-1H-pyrrole-3-carbonitrile is a white crystalline powder that has a pyrrole ring structure. It has been found to be stable in air and light, but not soluble in water. The infrared absorption spectrum of this compound shows bands at 3140 cm−1, 1650 cm−1, 1560 cm−1, and 880 cm−1. 2-Amino-5-(2-fluorophenyl)-4-methyl-1H-pyrrole-3-carbonitrile is not soluble in water but can be dissolved in methanol or ethanol. It is an organic chemical with a molecular weight of 198.2 g/mol and a melting point of 184°C.</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>4-Amino-N-methoxy-N-methylbenzamide is a ligand that has been used to catalyze the aminocarbonylation of iodides with phosphine. It has been shown to be stable in air and water, and is active under heterogeneous conditions, such as in the presence of palladium on carbon. 4-Amino-N-methoxy-N-methylbenzamide is also a ligand for the palladium, which can be used to catalyze carbonylative coupling reactions. This ligand has shown high activity for aryl bromides.</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>2-(Ethoxymethylidene)-3-oxobutanenitrile (EMC) is a programmed, activated, and caspase-trifunctional synthetic compound. It has been shown to induce apoptosis in leukemia cells by inhibiting the mitochondrial membrane potential and activating reactive oxygen species. EMC also induces death in tumour cells by inducing the release of cytochrome c from mitochondria into the cytosol, which activates caspases. EMC binds to 2-nitrobenzaldehyde (2-NBA) to form a stable complex that inhibits the enzyme nitroreductase, which is involved in carcinogenesis. The binding of 2-NBA also prevents the formation of reactive intermediates that would otherwise undergo spontaneous reactions and cause cell damage.</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>