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>2,6-Dichloropyridine-3-carboxamide is a boronic acid that is used in organic synthesis. It is a cross-coupling partner in Suzuki and Sonogashira reactions. 2,6-Dichloropyridine-3-carboxamide can be prepared by the reaction of an aryl boronic acid with 2,6-dichloropyridine. This reaction proceeds smoothly at room temperature and has been shown to proceed with high yield. The compound was also found to inhibit tyrosine kinase activity when expressed in cells. It is an organometallic molecule that contains a pyridinium group and an alkene section. The metathesis reactions of this compound have been studied extensively and it has been shown to undergo both metathesis reactions under different conditions.</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>But-1-yn-1-yltrimethylsilane is a sulfonation byproduct that can be found in tetrahydrofuran. It is an organic compound with the formula CH3(CH2)3SiOSO3H. This product has been shown to produce sulfonate, which is a keyword for this product.</p>

<p>Cyclohex-2-ene-1-carboxylic acid is a solute that is soluble in water. It has a molecular weight of 142.11 g/mol and a boiling point of 169°C. It is also soluble in ethanol, ether, chloroform, and acetone. Cyclohex-2-ene-1-carboxylic acid is synthesized from the hydrolysis of cyclohexane carboxylic acid via the hydration reaction with water. The hydroxy group on the molecule makes it an excellent solvent for various organic compounds as well as lipids and proteins.</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-Chloro-5-phenyloxazole is an organic compound that belongs to the class of c2-6 alkenyl, acyloxyalkyl, and formyl compounds. It is also a carboxylic acid derivative. 2-Chloro-5-phenyloxazole has been shown to be active against bacteria such as Staphylococcus aureus and Pseudomonas aeruginosa. This drug has been shown to have antibacterial properties against a variety of organisms, including gram positive and gram negative bacteria.</p>

<p>Methyl 9H-purine-6-carboxylate is a methyl ester of a purine. It is an organic compound that can be synthesized from the corresponding amine by reacting it with methanol and carbon monoxide in the presence of a palladium catalyst. The methyl group on this molecule is a substituent that has been shown to increase the rate of reaction with diazonium salts, which are used in the synthesis of other purines. This ester is also used as a precursor for the synthesis of other purines.</p>

<p>4-Oxo-4-(pyridin-2-ylamino)butanoic acid is an amide compound that is synthesized by reacting a pyridine with butanoic acid. This heterocyclic compound has been shown to have magnetic properties and it can be used as a synthon to generate other heterocyclic compounds. 4-Oxo-4-(pyridin-2-ylamino)butanoic acid can be oxidized to form the nitrate salt. The square planar geometry of this molecule displays four chiral centers, which gives it the ability to bind to metal ions in order to form complexes. This chemical is also known as a ligand, because it binds reversibly with a metal ion, such as copper or silver.</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-Bromopicolinic hydrazide is a chemical compound that has antibacterial activity. It is active against bacteria like B. subtilis, P. pneumoniae, and S. aureus as well as fungi such as M. macrophomina and A. fumigatus. 4-Bromopicolinic hydrazide is effective against bacterial strains like phaseolina, K. pneumoniae, and C. sclerotium, but not against E. coli or other Gram-negative bacteria that have been shown to be resistant to ampicillin in vitro studies. It also has antifungal properties which are active against A. fumigatus and M. macrophomina in vitro studies.br&gt;br&gt;<br>4-Bromopicolinic hydrazide inhibits the synthesis of DNA by binding to the enzyme DNA polymerase and preventing it from making copies of the bacterial DNA during replication.br&gt;br&gt;<br>This drug has</p>

<p>Versatile small molecule scaffold</p>

<p>3-Ethylbenzenethiol is a chlorinated derivative of benzenethiol that is used as a reagent in organic synthesis. It has been used to synthesize potassium and copper chlorides, and it has also been used in the preparation of 2-iodobenzoic acid. 3-Ethylbenzenethiol is a strong bronchodilator with cataleptic properties that can be used to control coughs. It has been shown to have antitussive effects when given at high doses, with no adverse side effects.</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-Methoxymethyl-phenyl)-methanol is an inorganic chemical. It is a synthetic compound that has been used as an experimental result to study the effects of introducing chloride into mosquitoes. The nitro group on the molecule was found to be of particular interest, as it may be able to react with a variety of organic compounds, including pyrethroid insecticides. 4-Methoxymethyl-phenyl)-methanol can be synthesized by reacting methoxymethyl chloride with potassium hydroxide in a constant temperature reaction.</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-Amino-1-benzofuran-2-carbonitrile is a heterocyclic compound that belongs to the isothiocyanate family. It has been shown to be an analog of phenyl isothiocyanate by x-ray crystallography, and it reacts with selenium dioxide in a 1:1 ratio to form selenides. The reaction mechanism is believed to be analogous to the reaction of phenyl isothiocyanate, although this has not yet been confirmed. The reaction proceeds with a refluxing pyridine as solvent, which crystallizes on cooling.</p>

<p>Methyl 4-isothiocyanatobutanoate (MITC) is a synthetic insecticide that is used in agriculture and against pests of brassica plants. MITC has been shown to be toxic to human pathogens, such as Salmonella enterica, Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus. MITC has a high volatility and can be applied to the leaves of plants. It has also been shown to have microbicidal properties against insects that are resistant to other insecticides.</p>

<p>2-(2,5-Dioxo-2,5-dihydro-1H-pyrrol-1-yl)-3-phenylpropanoic acid is a chemical that can be used as a reactional or catalyst in the production of aspartame. It is synthesized from toluenesulfonic acid and l-aspartic acid. 2-(2,5-Dioxo-2,5-dihydro-1H-pyrrol-1-yl)-3-phenylpropanoic acid is also used in the production of other chemical substances such as sulfuric acid and phosphoric acid.</p>

<p>Versatile small molecule scaffold</p>

<p>2-Oxocyclopentane-1-carboxamide is an organic compound that is used in the synthesis of cycloalkanols. It has been shown to be a suitable catalyst for the asymmetric synthesis of hydroxyamides and cyclic alcohols. 2-Oxocyclopentane-1-carboxamide is an organocatalytic, catalytic reagent that can be used in chemoenzymatic reactions with a high degree of enantiopurity. It can also be used to produce chiral compounds, such as epoxides, oxazolidines, and hydrazones. This chemical has been shown to have yields up to 98%.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>6-Chlorothieno[2,3-b]pyridine is a mechanistic probe that can be used to rationalize the mechanism of organic reactions. It has been shown to undergo fragmentation in an electron-initiated reaction.</p>

<p>Versatile small molecule scaffold</p>

<p>3-Aminoquinolin-2-yl ethyl carbonate is a versatile compound that has various applications in different fields. It is commonly used for crystallization purposes, as it helps to facilitate the formation of crystals in chemical reactions. Additionally, it has antimuscarinic properties and can be used as an ingredient in medications like tolterodine tartrate, which is used to treat urinary incontinence.</p>

<p>3-(Bromomethyl)quinoxalin-2(1H)-one is an organic compound that reacts with a variety of aromatic amines and is obtained by condensation of phthalimide with piperidine. This white crystalline solid has been shown to be soluble in water, ethanol, acetone, and ether. The salt of this compound can be prepared by the reaction of 3-(bromomethyl)quinoxalin-2(1H)-one with sodium methoxide or sodium in dimethyl sulfate. 3-(Bromomethyl)quinoxalin-2(1H)-one is used as a reagent for the synthesis of other organic compounds.</p>

<p>3-Phenyl-2,3-dihydro-1H-indole is a dichlorophenyl that can be oxidized to yield ethylene. It has been shown to have pharmacological properties and potential use as a pharmacological agent. 3-Phenyl-2,3-dihydro-1H-indole is also an anilino heterocycle. It exhibits intestinal activity and coagulant properties.</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-Amino-2-phenylpropan-1-ol is a compound that is the product of the reaction between an amine and an aldehyde. It can be synthesized by reacting an amine with an aldehyde in the presence of hydrochloric acid, and it can be used to produce other compounds such as lysergic acid and 3-hydroxypropylamine. This compound has been shown to react with isocyanates to form oximes, which are useful in organic synthesis. 3-Amino-2-phenylpropan-1-ol also reacts with amines to form imines, which have been shown to have antihistamine effects on rats. 3-Amino-2-phenylpropan-1-ol has been modified structurally, including by modification of its chloride group or by formation of cyclic structures such as lactams or lactones.</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>(3R)-5-Oxothiomorpholine-3-carboxylic acid is a lactam antibiotic that inhibits the growth of bacteria by binding to ribosomes. It acts as an analogue of penicillin, but has a higher affinity for the ribosome. The chemical structure of (3R)-5-oxothiomorpholine-3-carboxylic acid consists of a trifluoroacetate ester at the 3 position, which is responsible for its acidic properties. This drug also contains two functional groups at the 5 position, which are responsible for its ability to interact with sulfoxides and eluting chemicals in chromatography. (3R)-5-Oxothiomorpholine-3-carboxylic acid is used in analytical chemistry as a model for other compounds with similar structures.</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-5-ethylthiophene is a brominated electron donor that has been used as an electron delocalizer in macrocyclic compounds. The electron delocalization is due to the coplanarity of the bithienyl and tetramer rings. 2-Bromo-5-ethylthiophene can be used for the synthesis of polymeric materials, such as polyimides, by lowering the melting point. It is also an excellent reagent for MALDI-TOF analysis in mass spectroscopy.</p>

<p>Versatile small molecule scaffold</p>

<p>4-(2-Dimethylamino-ethoxy)-phenylamine is a synthetic, sustainable, membrane lipid that can form hydrophobic liposomes. These lipids are amphiphilic and form lamellar phases with one or two layers of molecules. The cavity in these phases can be filled with water, which may be useful for optical microscopy. The polymerase chain reaction (PCR) catalyzes the replication of DNA and RNA strands using 4-(2-dimethylamino-ethoxy)-phenylamine to coat the surface of the DNA template strand. This process allows for amplification of small amounts of target DNA sequences for research purposes.</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>(2S)-3-Cyclohexyl-2-hydroxypropanoic acid is an organic compound with the chemical formula CHCHOHCOH. It is a white solid that is soluble in water and polar organic solvents. (2S)-3-Cyclohexyl-2-hydroxypropanoic acid has been used for the synthesis of phenylpyruvic acid, which is an intermediate for the production of pharmaceuticals. The molecule has an acidic hydrolysis, which can be carried out through a nucleophilic substitution reaction with cyanide ion. The product of this reaction is phenylacetaldehyde, which can be converted to benzaldehyde. This process is enantioselective because it produces only one chiral form of benzaldehyde from a racemic mixture.</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-Methoxyethyl)(pyridin-2-ylmethyl)amine is a coordination compound that has the ability to bind metal ions. It crystallizes in an orthorhombic system, and its color is light yellow. The oxygen atoms are bound to two halides, which are connected by four tetradentate ligands. 2-Methoxyethyl)(pyridin-2-ylmethyl)amine has a phenolic group with an oxygen atom that forms a molecule with a mononuclear ligand. This substance can be used as a ligand for coordination compounds.</p>

<p>1,2-Bis(4-methoxyphenyl)ethan-1-amine hydrochloride is an optical isomer of the industrial chemical 1,2-diaminobenzene. It has been shown to be a proton source in metal halides, and can be used as a kinetic probe of proton transfer reactions. The functionalities of this compound have been demonstrated by its ability to form carboxylic acids with different functional groups and isomers. The C=N bonds are highly reactive, which leads to the formation of diborane. This molecule has also been shown to be a competitive inhibitor of 6-membered ring enzymes such as reversed-phase HPLC and kinetically competitive inhibition.</p>

<p>1-(2-Bromophenyl)propan-1-one is a chemical compound that is generated from the reaction of bromobenzene and lithium. It is a useful intermediate for the synthesis of various organic compounds, such as cyclopentanones and butyllithium. The reaction proceeds through an intramolecular cyclization in which a ketone reacts with a lithium enolate to form a lactam.</p>

<p>Versatile small molecule scaffold</p>

<p>1-(3-Methoxyphenyl)ethylamine is an enantiomer of the amino acid phenylalanine, and it has been used in the synthesis of racemic drugs. The optical properties of 1-(3-methoxyphenyl)ethylamine are different from those of other amino acids and can be used to create a chiral environment. This molecule can also be used as a calcimimetic that stimulates bone formation by increasing osteoblasts. It also inhibits aminotransferases and increases the production of malic acid, which is important for the synthesis of lactic acid. In addition, this molecule can be used as an efficient method for asymmetric synthesis with organic solvents such as amines or crystallography.</p>

<p>6-Amino-5-oxohexanoic acid hydrochloride is a metabolite of the amino acid 6-aminohexanoic acid. It is excreted in the urine and can be detected by resonance spectroscopy, ion-exchange chromatography, and magnetic resonance spectroscopy. The metabolite has been found to have acidic properties, which can be determined by gas-liquid chromatography. 6-Amino-5-oxohexanoic acid hydrochloride can be used as a biomarker for cerebrospinal fluid and has also been used in biochemical studies to explore the equilibrium between ionized and nonionized forms of acids.</p>