Building Blocks

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Methyl 4-aminobenzoate hydrochloride is a compound that is soluble in water and has a molecular weight of 155.14 g/mol. The compound has an acidic nature, with the pKa being 2.5, which makes it a proton donor and an acid catalyst. It can be used to synthesize retinoic acid, which is used to treat acne, by reacting with glycinamide ribonucleotide. Methyl 4-aminobenzoate hydrochloride can also be used for sample pretreatment before analysis by gas chromatography (GC), liquid chromatography (LC) or mass spectrometry (MS). This compound is not highly polar and can therefore be dissolved in non-polar solvents such as hexane or dichloromethane. Methyl 4-aminobenzoate hydrochloride reacts with anthracene and amines to form methyl derivatives.</p>

<p>Versatile small molecule scaffold</p>

<p>1-Iodo-4-methoxy-2-methylbenzene (1IMMB) is an iodide which has been used as a precursor in the synthesis of carbonyl groups. This compound has also been shown to have high yields and mechanistic. The carbonyl group is located at the 1,3 positions and the methoxy group is located at the 2 position. This compound reacts with acetonitrile to form a naphthalene derivative. 1IMMB also reacts with an alcohol to form a cyclic ether with regiospecificity. It can also be used as a catalyst in the synthesis of unsymmetrical compounds that contain both carbonyl groups and alcohols.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1-(2-Ethylhexyl) 4-methyl benzene-1,4-dicarboxylate is a silylated, polysulphide sealant with good adhesion to many plastics and metals. It is also used as a plasticizer for acrylates and a sealant for polyurethanes. This product has been shown to be an effective sealant for terephthalate and polyethers. The molecule contains two ester groups that react with the hydroxyl groups on the surface of the substrate to form the crosslinked network.</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>8-Chloro-1H-benzo[D][1,3]oxazine-2,4-dione is an organic chemical used as a precursor to pharmaceuticals. It is produced by the esterification of an acid chloride with a carboxylic acid. This chemical can be converted into other products through hydrogenation or hydrochlorination. 8-Chloro-1H-benzo[D][1,3]oxazine-2,4-dione is also used in the production of xylene and dichlorobenzene. This compound has two isomers that differ in their reactivity due to steric hindrance. The less reactive isomer has been shown to have antiinflammatory effects in mice.</p>

<p>Cyclobutane-1,3-diol is an organic compound that is a viscous liquid at room temperature. It is used in the production of polyesters and coatings. Cyclobutane-1,3-diol has been shown to be a good ligation partner with ethylene glycol in the liquid phase. It also has been used as an impurity scavenger and as a skeleton for other compounds. Cyclobutane-1,3-diol can be purified by distillation or crystallization, but it may contain fluorine or alkali metal residues that are difficult to remove. There are two stereoisomers of cyclobutane-1,3-diol: D-(+)-cyclobutane-1,3-diol and L-(+)-cyclobutane-1,3-diol.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-(4-Nitrophenyl)-5-phenyl-1H-pyrazole is a dipole tautomeric proton tautomer with a fluorescence photophysical. It has a molecular orbital that is acidic. 3-(4-Nitrophenyl)-5-phenyl-1H-pyrazole has the following transfer functional groups: nitro, fluorescence, and photophysical. 3-(4-Nitrophenyl)-5-phenyl-1H-pyrazole is an experimentally determined molecule with a molecular orbitals of acidic. It has two tautomers, which are the dipole and tautomers. The dipole tautomeric proton tautomer is the more stable form of 3-(4-Nitrophenyl)-5-phenyl-1H-pyrazole in solution.</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-Bromo-3-methoxybenzoic acid is a fluorescent acridine that can be used as a reagent, an analogue of acridone, and a ligand for macrocycles. It can also be used to synthesize fluorophores that are glycols. 2-Bromo-3-methoxybenzoic acid is cyclised to form the acridine ring system with two methoxy groups on the 2 and 3 positions. The bromine atom on the 2 position is replaced by a hydrogen atom in the final product.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Ethyl 5-hydroxy-1,2-oxazole-3-carboxylate is an antidepressant drug that belongs to the isoxazole class of compounds. It has been shown to have antidepressant-like effects in a number of functional assays and animal models. This compound has been shown to bind with high affinity to nicotinic acetylcholine receptors as well as serotonin transporters. In addition, ethyl 5-hydroxy-1,2-oxazole-3-carboxylate prevents the reuptake of both acetylcholine and serotonin in rat brain synaptosomes. These results suggest that this compound may be useful for the treatment of depression and other neurological disorders related to neurotransmitter dysfunction.</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>4-(Methylsulfanyl)butanamide is a chiral compound that is derived from the amino acids valine, threonine, and methionine. It has been shown to inhibit the growth of Rhodococcus erythropolis in culture by blocking nitrile synthesis and hydrolysis. The mechanism of action for 4-(methylsulfanyl)butanamide is not clear. However, it has been shown to contain sequences related to those found in other amino acid sequences that are known to be involved in cell division.</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-Bromo-4-methylheptane is a chiral molecule with two stereogenic centers. It has been used as a pheromone in the study of insect behavior, and has been shown to have a similar effect on humans. It has been found that human subjects responded more strongly to an enantiomeric mixture than to either of the pure enantiomers. This suggests that 1-bromo-4-methylheptane is a racemate, or a molecule with two different configurations.</p>

<p>5-Fluoro-8-methylquinoline is a catalytic agent that participates in the formation of 8-methylquinoline. It is prepared by reacting benzyl chloride with ethanolamine in the presence of phosphine, chlorine and catalytic amounts of iodine. The reaction product is purified by fractional distillation to yield 5-fluoro-8-methylquinoline. This compound can also be synthesized from chlorination of cyclic or carbonyl compounds with phosphine and chlorine, as well as from iodides and sulfate.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>5-Chloro-1H-[1,2,3]triazole-4-carbonitrile is a chemical compound that can be prepared by reacting ethyl orthoformate with an acetal of ethylene. This chemical compound has the formula CHClN and can be described by three isomers, namely 5-chloro-1H-[1,2,3]triazole-4-carbonitrile, 5-chloro[1,2,3]-triazole-4-carbonitrile and 5-[1,2,3]-triazole-4-carbonitrile. It has been used in the synthesis of ethylene acetals as well as in alkylation reactions to produce ethyl orthoformates. The reaction product of this chemical compound with methyl iodide produces acetaldehyde dimethylacetal. This chemical compound also reacts with diethylzinc to form methyl azide and diethyl ether.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>5-Amino-2-methoxybenzenesulfonamide is an optical copolymer that belongs to the group of liquid crystalline polymers. It consists of a chiral, thermotropic monomer and a copolymerized, non-chiral monomer. 5-Amino-2-methoxybenzenesulfonamide has a crystal melting point of 195°C and is soluble in organic solvents. This polymer has been shown to form liquid crystalline phases with different optical properties depending on the composition of the mixture.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-Methylisothiazole-5-carboxaldehyde is a potent antiviral agent that has been shown to be active against human viruses in vitro. It has also been shown to have an inhibitory effect on the infectivity of influenza virus in mice. 3-Methylisothiazole-5-carboxaldehyde prevents the virus from penetrating the cell membrane, thereby preventing viral replication and inhibiting the release of new viruses into the host. This compound can be used as a chemotherapeutic agent for respiratory infections because it is orally bioavailable and inhibits viral replication.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Pyrimidine-2-carboxamide is an amide that has been shown to have antiinflammatory activity. It has been clinically studied for the treatment of diabetic neuropathy, inflammatory bowel disease, and autoimmune diseases. Pyrimidine-2-carboxamide inhibits the production of proinflammatory cytokines by inhibiting hydrogen bond formation between the amide group and DNA bases. This compound also has a number of other biological activities, including antiviral effects against HIV infection and cancer. Pyrimidine-2-carboxamide is a chemotherapeutic agent that has been used in clinical trials for bladder cancer and bowel disease.</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-(Methoxymethyl)benzoic acid is a natural product that has been shown to have antibacterial activity. It is an ethylene precursor and is synthesized by the alkaline hydrolysis of 2-hydroxybenzoic acid. 2-(Methoxymethyl)benzoic acid has been shown to inhibit the growth of bacteria, such as E. coli, in the presence of hexanoic or octanoic acids. This compound also inhibits the growth of other bacterial species, including lamiaceae and eugenol, at low concentrations. The inhibitory effect may be due to its ability to bind to hydrophobic sites on bacterial cell membranes. 2-(Methoxymethyl)benzoic acid acts as a phenolic compound with a hydrocarbon group.</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>Ethyl 2-(carbamoyloxy)benzoate (EMCB) is a prodrug that is hydrolyzed in vivo to the active form, fenoprofen. It has been shown to inhibit prostaglandin synthesis and to have analgesic, antipyretic, and anti-inflammatory properties. EMBC inhibits the enzyme cyclooxygenase which converts arachidonic acid into prostaglandins. In humans, EMBC is absorbed from the gastrointestinal tract and excreted in the urine unchanged or as metabolites. The drug has been found to be effective against activated platelets and plasma albumin, but not against intestinal enzymes such as ileal or pancreatic amylases. EMBC also has contraceptive properties and can be used as an oral contraceptive for up to three months at a time. EMBC may interact with other drugs that are broken down by cytochrome P450 enzymes, including acetylsalicylic acid and corticoster</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>