Building Blocks

<p>2-Aminocarbonylnicotinic acid is a nicotinic acid amide with a 3-quinolinecarboxylic acid moiety. It is synthesized by the reaction of isocyanates and succinamide, followed by cyclization. 2-Aminocarbonylnicotinic acid has been used to produce benzoic acids, amides, and dicarboxylic acids. This compound has also been shown to be an effective inhibitor of bacterial growth in vitro. 2-Aminocarbonylnicotinic acid is an unsubstituted molecule that can be used as a starting material for the synthesis of other compounds.</p>

<p>Versatile small molecule scaffold</p>

<p>The herbicide 3-Hydroxy-2-phenylcyclopent-2-en-1-one is a phenoxy compound that inhibits the enzyme acetolactate synthase, which is required for the biosynthesis of branched chain amino acids. This inhibition leads to a shortage of these amino acids and growth inhibition in plants.</p>

<p>The compound 2,4-dimethylpentanoic acid is a monocarboxylic acid that can be used as a conditioner in refrigeration fluids. It has been shown to have a significant effect on the fluid's ability to transfer heat by lowering its viscosity. This compound is also an acid catalyst that has been used in the production of polyesters and other plastics. The carboxyl groups on this substance allow it to act as a weak base.</p>

<p>Versatile small molecule scaffold</p>

<p>3-Aminoquinolin-2(1H)-one is a synthetic compound. It has been prepared by condensation of 2-aminoacrylic acid with 1,3-diaminopropane. This reaction yields an imine that can be hydrolyzed to the corresponding amine. 3-Aminoquinolin-2(1H)-one has been used as an efficient method for the synthesis of hippuric acid and its isomers. The spectra of 3-aminoquinolin-2(1H)-one show three peaks at m/z=193, 182 and 144, which correspond to the molecular ion peak (m/z=193), the corresponding methylene peak (m/z=182) and the protonated amine peak (m/z=144). The mass spectrum shows two major peaks: one at m/z=193 and one at m/z=145. These peaks are due to fragmentation</p>

<p>2-Ethynylcyclohexan-1-ol is a cyclohexanol derivative that is synthesized by the intramolecular coupling of two phenylsulfonyl acetates. It has been shown to be an acid and base conjugate. 2-Ethynylcyclohexan-1-ol has a photophysical profile that includes fluorescence, which makes it useful for detection. This compound also yields ketones and carbocycles, making it useful in synthesis.</p>

<p>N,N-Diethylaniline hydrochloride is an organic chemical compound that is a derivative of aniline. It is used as a precursor to other chemicals and as a polymerization initiator. N,N-Diethylaniline hydrochloride has been shown to be soluble in chloroform and ethanol, insoluble in water. The processability of this compound can be improved by the addition of chlorine or cyclopentadienyl chloride to the reaction vessel. This chemical has a high melting point and is soluble in certain solvents.</p>

<p>2-[Acetyl(methyl)amino]acetic acid is a serine protease inhibitor that has been shown to be effective against inflammation. It is an organic compound with the chemical formula CH3CO2CHCONH2. 2-[Acetyl(methyl)amino]acetic acid has a hydroxyl group, two fatty acids, and an intramolecular hydrogen bond. The alkylsulfonyl group and the sulfonic acid group are attached to the hydroxy group on one side of the molecule. This drug inhibits the activity of serine proteases by blocking their active site.</p>

<p>Versatile small molecule scaffold</p>

<p>N-tert-Butylbenzamide is a functional group with the chemical formula C6H10N2O. It has the amide, n-oxide and chloride functional groups. N-tert-Butylbenzamide is synthesized by reacting an aromatic hydrocarbon with an acid catalyst in the presence of aluminium. The reaction mechanism for this chemical is nucleophilic substitution. NMR spectra are used to identify the product formed by this reaction and to determine its purity. This efficient method of synthesis can be applied to other organic compounds as well.</p>

<p>3-Iododibenzofuran is a fluorescent compound that has been used as a probe for the study of neutral endopeptidase activity. The compound is characterized by a high degree of thermal stability and an inhibitory potency at pH 7.0 that is approximately 3 orders of magnitude greater than that of the active site inhibitor, anthracene. 3-Iododibenzofuran can be synthesized using chemoenzymatic methods, with efficiencies and profiles that are similar to those obtained in the conventional method. This probe can also be used to investigate the functional role of proteins in living cells or tissues.<br>3-Iodobenzofuran has been shown to have pressor effects in rats and can cause tetrazole (a type of explosive) to detonate when heated, which makes it unsuitable for use in devices such as explosives or pyrotechnics.</p>

<p>5-bromo-3-methylfuran-2-carboxylic acid (BMFC) is a furan that acts as a catalyst for the isomerization of ethyl diazoacetate to methyl diazoacetate. BMFC is also used in organic synthesis, specifically as an intermediate in the production of pharmaceuticals.</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-Acetamido-4-chlorobenzoic acid is a synthetic drug that is used as an ester in pharmaceuticals. It was first synthesized in 1958 and has been shown to have tuberculostatic activity, but it does not bind to DNA or RNA. 2-Acetamido-4-chlorobenzoic acid inhibits protein synthesis by binding to the 30S ribosomal subunit, inhibiting peptidyl transferase. It also inhibits bacterial growth by binding to the 50S ribosomal subunit and competes with aminobenzoic acid for binding sites on the enzyme alcohol dehydrogenase.<br>2-Acetamido-4-chlorobenzoic acid is used in veterinary medicine as a treatment for Mycobacterium avium complex (MAC), which causes chronic respiratory disease in cats. The drug has also been shown to inhibit cancer cells by interfering with cell division at the G2/M</p>