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>

<p>Versatile small molecule scaffold</p>

<p>Tadalafil is a synthetic drug that is used as a treatment for erectile dysfunction. It works by inhibiting the PDE5 enzyme, which is responsible for breaking down cGMP. Tadalafil has been shown to be effective in the treatment of male erectile dysfunction and pulmonary hypertension, with few side effects. This drug is taken orally, with a meal or without one, and can be administered with or without food. To improve absorption, tadalafil should be taken at least 30 minutes before sexual activity. The dosage of tadalafil ranges from 2.5 to 20 mg, and it should not exceed 40 mg per day.</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-Pyridin-2-yl)piperidin-4-amine is a drug that acts as an anorexiant. It binds to the serotonin 5HT3 receptor, which is involved in the regulation of appetite and mood. It also blocks the action of serotonin at the 5HT4 receptor, which is involved in mediating intestinal motility. This agent has been shown to have a potent antagonist effect on the 1-4c alkyl group of serotonin receptors. The phenoxy group and methyl group are also responsible for binding with serotonin receptors and blocking their activity.</p>

<p>Versatile small molecule scaffold</p>

<p>2-Amino-3-methoxypropanoic acid hydrochloride is a mitochondrial enzyme inhibitor that is used as a research tool to study protein synthesis. It binds to the cytochrome b2 subunit of the mitochondrial respiratory chain, inhibiting the oxidation of pyruvate and affecting the production of ATP. 2-Amino-3-methoxypropanoic acid hydrochloride has been shown to induce apoptosis in human liver cells by triggering caspase 3, which is an important enzyme in the apoptotic pathway. 2-Amino-3-methoxypropanoic acid hydrochloride also has a number of chemical properties that make it useful for analytical chemistry. For example, 2-amino-3-methoxypropanoic acid hydrochloride can be used to measure carboxylic acids, acetylation reactions, hydrogen bonds and hydroxyl groups. It can also be used as a nucle</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-(Morpholin-4-yl)acetyl chloride hydrochloride is a fine chemical that is used as a building block for the synthesis of other compounds. It can be used in research and development, or as a reagent. 2-(Morpholin-4-yl)acetyl chloride hydrochloride has high purity and is easily soluble in water. This compound can be used as an intermediate to synthesize other compounds, or it can be used as a scaffold for the formation of complex structures.</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-(1H-Pyrazol-4-yl)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidine is a synthetic compound that can be used to discriminate between the left and right hands of the body. It has been shown to have a high affinity for the enzyme kinases with an IC50 of 0.5 μM. 4-(1H-Pyrazol-4-yl)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidine has been used as a tool in elucidating the mechanism of action of these enzymes by measuring their kinase activity and identifying their substrate specificity. It also has applications in inflammatory diseases as it shifts immune cells from a proinflammatory state to an antiinflammatory state.</p>

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<p>(2S)-3-Hydroxy-2-phenylpropanoic acid is an unlabelled, naturally occurring compound. It is the citric acid analog of L-phenylalanine. The structure of (2S)-3-Hydroxy-2-phenylpropanoic acid is a skeleton that consists of one hydroxyl group and one carboxylic acid group. The carboxylic acid group has a double bond in the alpha position to the carboxyl carbon, which gives this molecule an acidic character. The chloride ion is also present in this structure. This molecule can be synthesized by a kinetic reaction that involves fatty acids and brugmansia as catalysts. It can also be synthesized through a catalysed reaction using thionyl chloride as a catalyst.</p>

<p>2-Hydroxy-3-(1-methylethyl)-butanedioic acid is an organic compound that is a metabolite of the amino acid methionine. It is formed by the oxidation of the methyl group on the 2 position in methionine. The protein subunits are expressed in liver cells and it has been shown to have antioxidant properties. The analytical methods used for this compound include LC-MS/MS, which separates it into its individual isomers. This method can be used to determine the purity of 2-hydroxy-3-(1-methylethyl)-butanedioic acid. The carbonyl group in this molecule makes it susceptible to steric interactions with other molecules, which may lead to it being oxidized or reduced. It has been found that 2-hydroxy-3-(1-methylethyl)-butanedioic acid shows thermophilic and enterocolitic properties.</p>

<p>N-Carbethoxy-4-hydroxypiperidine is a drug substance that is a h1 receptor antagonist. It is used as an antihistamine to treat the symptoms of hay fever and other allergic reactions. N-Carbethoxy-4-hydroxypiperidine is available in two enantiomers, or mirror images, which are labelled S and R. The R enantiomer is more potent than the S enantiomer for inhibiting histamine h1 receptors. This drug has been shown to inhibit the growth of tuberculosis bacteria in cell culture and animal models, but not against Mycobacterium avium complex. N-Carbethoxy-4-hydroxypiperidine has also been shown to have significant antibacterial activity against Clostridium perfringens with minimal toxicity in mice.</p>

<p>Versatile small molecule scaffold</p>

<p>3,4-Dihydroxyphenylalanine (3,4-DOPA) is a non-protein amino acid that is an intermediate in the synthesis of dopamine and norepinephrine. 3,4-DOPA is metabolized by the enzyme dopa decarboxylase to dopamine and then by catechol-O-methyl transferase to norepinephrine. 3,4-DOPA has antioxidant properties and has been shown to have anticancer effects in animals. It also has been shown to interact with other biomolecules such as proteins and nucleic acids. 3,4-DOPA binds strongly to metal ions through its carboxylic acid group and can chelate metals such as copper or iron. This property may be used for coatings on metal surfaces or for interacting with other molecules.br&gt;br&gt; 3,4-Dopa contains a chiral center due to the presence of two stereogenic carbons on the phen</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Ethyl 3-formyl-1H-pyrrole-2-carboxylate is a formyl compound with the molecular formula C8H8O3. It is a colorless liquid that has a strong odor. The compound can be obtained by the reaction of ethyl acetoacetate and pyrrole in the presence of aluminum chloride. The compound has been studied for its nuclear magnetic resonance (NMR) properties. It has two conformers, which are distinguished by their different chemical shifts, and this difference can be used to study coupling between the carbonyl group and other groups in the molecule.</p>

<p>1-chloro-4-fluoroisoquinoline is a chlorinating agent that has been used as a synthetic method for the synthesis of oxychloride. It is typically used in the presence of palladium catalyst, in the presence of phosphorus and under reductive conditions. The chlorination reaction is initiated by addition of hydrochloric acid or phosphorous oxychloride. The 1-hydroxyisoquinoline reacts with phosphorus to form a chloroformate, which reacts with fluorine gas to produce an intermediate chlorofluorinate. This intermediate then reacts with chlorine gas in the presence of palladium catalyst to generate the desired product, 1-chloro-4-fluoroisoquinoline.</p>

<p>Versatile small molecule scaffold</p>

<p>3,5-Bis(trifluoromethyl)-1H-pyrazole-4-carboxylic acid is a chiral compound that has been shown to be an active building block for coordination frameworks. It is prepared from the reaction of 3,5-bis(trifluoromethyl)-1H-pyrazole with a carboxylic acid and can be used in the synthesis of metalloporphyrins. 3,5-Bis(trifluoromethyl)-1H-pyrazole-4-carboxylic acid has been shown to form stable coordination complexes with ligands such as bidentate or tridentate phosphoramidites and dimethylammonium chloride. This compound undergoes thermal treatment during the preparation process and reacts with various solvents and reagents.</p>

<p>3-Methoxythiophene-2-carbaldehyde is a ligand that has been shown to form a stable complex with potassium chloride. This compound is also reactive, and can be stabilized in the reaction vessel. In the presence of sulfate ions, 3-methoxythiophene-2-carbaldehyde will react to form a phosphotungstic acid precipitate. The dehydrated salt can be recrystallized by adding phosphotungstic acid, which stabilizes the product.</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>Benzyl N,N,N',N'-tetraisopropylphosphorodiamidite is a reagent that reacts with hydroxybenzyl amine to form an ester. This product is used for the synthesis of phosphoramidites and benzyl esters. It is also used as a catalyst for the synthesis of diesters.</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>2,2',4,4'-tetrahydroxybenzophenone is a hydroxylated benzophenone that has immunomodulatory effects. It binds to the receptor in the immune system and can cause an increase in cytokine production. 2,2',4,4'-tetrahydroxybenzophenone is cytotoxic and has significant toxicity in vitro. The molecule has been shown to disrupt mitochondrial membrane potential. This may be due to its ability to form hydrogen bonds with molecules on the mitochondrial membrane. 2,2',4,4'-tetrahydroxybenzophenone also modulates transcriptional regulation of genes involved in cell proliferation and apoptosis. The drug is detectable at low levels by mass spectrometry and is not known to have any toxicological effects.END&gt;&gt;</p>

<p>2,4,6-Trichloropyrimidine is an antimicrobial agent that belongs to the chemical class of pyrimidine compounds. It inhibits bacterial growth by cross-linking with amino acids and nucleic acids in the cell wall, thereby inhibiting protein synthesis. 2,4,6-Trichloropyrimidine is also a cross-linking agent for polymers such as polyurethane and vinyl chloride. This compound has been shown to be effective against P. aeruginosa and other bacteria that are resistant to antibiotics. 2,4,6-Trichloropyrimidine reacts with water vapor or oxygen nucleophiles to form hydrogen chloride and amine groups. These reactions can be used for identification of this compound in the laboratory.</p>

<p>1-Trityl-1H-imidazole-4-carbaldehyde is a phosphorane that has been synthesized in the laboratory. It is an organometallic compound with a chloroformate ligand and a mononuclear, dimethylformamide complex. 1-Trityl-1H-imidazole-4-carbaldehyde has shown to be an electrophile and binds to receptor sites with high affinity. This may be due to its ability to form hydrogen bonds with the receptor site, which often occurs for pharmacokinetic profiles.</p>

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<p>Metal-chelating agent</p>

<p>2,3-Pyridinedicarboxylic acid dimethylester (PDDE) is a methylated derivative of 3-nitrophthalic anhydride. It has been shown to be a stereoselective receptor blocker that binds to the glutamate site of the N-methyl-D-aspartate receptor. PDDE has also been shown to have high affinity for the cerebral cortex and is able to penetrate the blood brain barrier. PDDE blocks the NMDA receptor by binding to it and preventing ion flow, which leads to inhibition of neurotransmitter release. This drug is used as an injectable methyl derivative with a molecule weight of 217. The ionization detector can detect PDDE in tetrahydrofuran at concentrations of 1,000 ng/mL or less.</p>

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<p>2-Mercapto-N-methylbenzamide is a synthetic compound that has been shown to have inhibitory activities against activated brain cells and cell lines. This drug has been used in the synthesis of axitinib, a cancer drug that inhibits cellular growth. 2-Mercapto-N-methylbenzamide is also used as a preservative in cosmetics and can be found in carbonated drinks and foods. It has been shown to inhibit the production of serotonin in microbicidal reactions by inhibiting the enzyme hydroxymethyl transferase, which catalyzes the conversion of 5-hydroxytryptophan to serotonin. It also prevents the reaction products from being formed by reacting with hypoxanthine, xanthine, and phosphoribosyl pyrophosphate (PRPP). 2-Mercapto-N-methylbenzamide also reacts with plasma samples to form ethylmercaptoacetate, which is then oxidized to merc</p>

<p>Methyl 3,4-dimethoxybenzoate is an acetate extract that has been shown to inhibit tyrosinase activity. This compound also has a potent inhibitory effect on the production of p-hydroxybenzoic acid. Methyl 3,4-dimethoxybenzoate can be synthesized from protocatechuic acid and methoxy groups. It is a chemical reaction involving three steps: condensation, dehydration, and reduction. Tyrosinase is an enzyme in the melanin biosynthetic pathway that catalyzes the conversion of tyrosine to dopaquinone. Tyrosinase activity can be inhibited by methyl 3,4-dimethoxybenzoate through competitive inhibition or by its ability to reduce the availability of substrate for this enzyme.</p>

<p>1-Methyl-1,2,4-triazole is a molecule containing nitrogen atoms. It can be used as a monomer in the preparation of polymers or materials. 1-Methyl-1,2,4-triazole has been shown to be effective for the equilibration of mixtures of organic compounds in analytical methods and matrix effect studies. The reaction vessel must be unsymmetrical to prevent the polymer from sticking to it and causing potential problems with the separation process.</p>

<p>Leu-Leu-Leu-OH is a pentapeptide that is used in cancer treatment to inhibit the growth of cancer cells. It prevents the production of proteins and, as a result, cell division. Leu-Leu-Leu-OH has been shown to be effective against tumor cells with an antibody that binds to the surface of cells. The monoclonal antibody is taken up by the cancer cells through receptor mediated endocytosis, which leads to inhibition of protein synthesis and cell death.</p>

<p>N-alpha-Z-L-lysine methyl ester hydrochloride is a preparation that is used as a methyl ester. It is an ester of lysine and methyl chloride. This product has a molecular weight of 170.16 g/mol and the chemical formula CH3CONHCH2CH(NH)CO2CH3. The structural data has not been confirmed by X-ray crystallography, but it can be assumed to be in the form of a zwitterion. N-alpha-Z-L-lysine methyl ester hydrochloride can be used for the synthesis of peptides, which are building blocks for proteins and enzymes. N-alpha-Z-L-lysine methyl ester hydrochloride is also used in the production of certain kinds of drugs and organic acids such as acetylsalicylic acid (aspirin).</p>

<p>Isocytosine is a prodrug that has been synthesized with the intramolecular hydrogen on the nitrogen atoms, which makes it more chemically stable. Isocytosine is a reactive molecule, and can react with tautomers to form isocytosine derivatives. Isocytosine contains three hydrogen atoms that are transferable through reactions to other molecules. The chemical stability of isocytosine allows for its use in wastewater treatment. It also has metabolic effects, such as the inhibition of colorectal adenocarcinoma and metabolic disorders. Isocytosine can be used as a model system for studying transfer reactions and reaction mechanisms.</p>

<p>2-Iodobenzoic acid is a synthetic compound that is used in the treatment of wastewater. It is produced by the reaction of benzoate and nitrite in the presence of sodium hydroxide. The intramolecular hydrogen atom transfer from the 2-iodobenzoic acid to benzoate is a reversible reaction. This process can be catalyzed by palladium, which has been shown to be effective in coupling 2-iodobenzoic acid with other compounds to produce cyclic peptides. The use of 2-iodobenzoic acid as a contraceptive has been investigated for its ability to inhibit acetylcholinesterase activity, which may lead to increased levels of acetylcholine and inhibition of muscle contractions.</p>

<p>2-Iodobenzoic acid methyl ester is a palladium complex that can be used as a catalyst for the hydrolysis of ketoesters, imines, and halides. The reaction mechanism involves the coordination of the metal center to the carboxylate or amine group on the substrate, followed by a nucleophilic attack at the benzoate or chloride group. The resulting product is an alkyl halide. 2-Iodobenzoic acid methyl ester has been shown to catalyze the cross-coupling of diphenyl ethers with various amines in water and in organic solvents.</p>

<p>Versatile small molecule scaffold</p>

<p>5-Hydroxypyrazine-2-carboxylic acid is a drug that inhibits the activation of proteins involved in cell signaling pathways. It has been shown to have an inhibitory effect on the activation of protein kinase C, which plays a key role in the proliferation and differentiation of cells. 5-Hydroxypyrazine-2-carboxylic acid also inhibits sorafenib, a drug used for the treatment of cancer. Sorafenib is metabolized in rats by cytochrome P450 (CYP) enzymes, which are found in human liver tissue as well. The metabolism rate of sorafenib can be reduced by coadministration with caffeine or other substances that induce CYP activity. 5-Hydroxypyrazine-2-carboxylic acid is not active against pyrazinoic acid and pyrazine-2 carboxylate, which are metabolites produced by CYP enzymes.</p>

<p>Versatile small molecule scaffold</p>

<p>Used in the preparation of metal-diene reagents (e.g. for carbocyclization)</p>

<p>Trans-1,2-Dichloroethylene is a chlorinated hydrocarbon that is used in the production of polyvinyl chloride plastics. When ingested at dietary concentrations, trans-1,2-Dichloroethylene may cause liver damage and death in CD-1 mice. Trans-1,2-Dichloroethylene has been shown to react with nucleophilic substitutions and produce toxic reaction products. This chemical also causes polymerase chain reactions that can lead to cell death. The effective dose for this chemical is unknown because it has not been tested in clinical trials.</p>

<p>1,1-Dibromo-2,2-bis(chloromethyl)cyclopropane is a synthetic chemical that can be used to synthesize lactams. It is a member of the class of enolates and has two isomers: sulfoxide and sulfone. The synthesis process begins with an amination reaction between 1,1-dibromo-2,2-bis(chloromethyl)cyclopropane and an amine in the presence of magnesium chloride. This reaction produces a sulfide intermediate that reacts with an aldehyde or ketone to form the desired lactam. The reaction time varies depending on the reactivity of the reactants, but it typically takes less than one hour at room temperature. Magnesium metal is needed as a catalyst for this reaction because it will not take place without it. 1,1-Dibromo-2,2-bis(chloromethyl)cyclopropane also reacts easily</p>

<p>2,2'-Dithiodianiline is a redox-active molecule with a redox potential of -0.08 V. It has been shown to inhibit the polymerase chain reaction by binding to DNA and inhibiting the enzyme DNA polymerase. 2,2'-Dithiodianiline is a potent inhibitor of bacterial growth in vitro, and has been shown to be cytotoxic in vivo. 2,2'-Dithiodianiline inhibits the growth of resistant mutants that are resistant to other antibiotics such as penicillin and ampicillin. This compound binds to molybdenum at an optimum concentration of 0.5 mM and coordinates through electrostatic interactions with the molybdenum atom. Structural analysis reveals that 2,2'-dithiodianiline forms hydrogen bonds with adenine residues in DNA and interacts with guanine residues in RNA through π-π stacking interactions. This interaction prevents transcription by blocking the binding</p>

<p>3-(Difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylic acid is a synthetic chemical that is used as a pesticide. This chemical has been found to be more effective than other pesticides because it can inhibit the synthesis of fatty acids, which are necessary for the growth of insect larvae. 3-(Difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylic acid is synthesized by reacting sodium hydroxide solution with triethyl orthoformate in the presence of hexamethylenetetramine. This reaction produces a mixture of diethyl ester and carboxylate esters, which are then separated from each other. The resulting carboxylate ester is then oxidized to produce 3-(difluoromethyl)-1-methyl-1H pyrazole 4 carboxylic acid.</p>

<p>Diiodomethane is a chemical compound with the molecular formula CHI. It is a colorless gas that can be obtained by reacting methyl ethyl and hydroxyl group in the presence of an oxidant such as boron nitride. Diiodomethane has been used as a substrate film for n-dimethyl formamide and reaction solution, which have been studied using spectroscopic data. The product of this reaction is water vapor that leaves the system due to its low boiling point. Reaction mechanism for this process is thought to be due to the kinetic energy of the particles that collide and produce diiodomethane molecules.</p>

<p>2,4-Dibromothiazole is a nicotinic acetylcholine receptor (nAChR) antagonist which selectively blocks the binding of acetylcholine to nAChRs. It has been shown to be effective in treating inflammatory bowel disease by inhibiting the production of inflammatory mediators. This drug also has anti-inflammatory effects and can be used for the treatment of autoimmune diseases such as Crohn's disease. 2,4-Dibromothiazole also has low energy properties and is used in palladium complexes for cross-coupling reactions. It can also be used as a cancer chemotherapeutic agent and as a cardiac drug.</p>

<p>4,6-Dichloro-5-nitropyrimidine is an intermediate in the synthesis of Tenofovir, a nucleophilic drug that inhibits HIV. It is produced by the reaction of chloride with amines and nitro compounds in the presence of ammonium chloride. 4,6-Dichloro-5-nitropyrimidine has been shown to have anticancer activity against human lymphocytes and other cancer cells. It can also be used for the treatment of AIDS. The biological properties of this compound are dose dependent and are dependent on the size of chlorine atoms attached to nitrogen atoms.</p>

<p>2,4-Diamino-5-nitropyrimidine is a synthetic molecule that belongs to the class of heterocyclic amines. It has been shown to be a potent antiproliferative agent and has been found to inhibit hepg2 cell growth in vitro. This compound was also found to inhibit cancer cells, including mcf-7. 2,4-Diamino-5-nitropyrimidine binds nucleophilic sites on proteins and inhibits enzymes involved in DNA synthesis. The inhibition of these enzymes leads to cell death by preventing the production of new proteins needed for cell division.</p>

<p>4,4'-Diamino-2,2'-bipyridine (DABP) is a redox-active compound that is synthesized to be used as a single-stranded DNA probe. It has been shown to have high affinity for nucleic acids and can be used in many applications including the detection of mutations in human ovarian carcinoma cells. DABP can also be used as a model protein for studying interactions with other biomolecules. The immobilization of DABP on an electrode surface allows for the study of its electrochemical properties. This includes the correlation between the redox potential and luminescence intensity and the dependence on pH or ionic strength. DABP can also be used to detect oxygen concentration or ATP levels in mitochondria through its ability to absorb light at wavelengths from 400 nm to 800 nm which is then converted into light at lower wavelengths by uv irradiation.</p>

<p>2,5-Dibromo-3-aminopyrazine is an experimental drug with anticancer activity. It has been shown to have a high affinity for DNA and inhibit the growth of tumor cells in vivo. 2,5-Dibromo-3-aminopyrazine has undergone stability tests in vivo and in vitro and also completed clinical trials. This drug binds to DNA and inhibits the enzyme protein kinase C, leading to suppression of cellular proliferation. The pharmacokinetics of this drug were evaluated by measuring the concentration of 2,5-dibromo-3-aminopyrazine in plasma after oral administration to mice. This study found that the maximum concentration was achieved at 1 hour post dose and that there was a decrease in concentration over time. The drug has been shown to bind to the dimethoxybenzene metabolic pathway, which is involved in regulating cell proliferation.<br>2,5-Dibromo-3-aminopyrazine</p>

<p>1-Cyano-4-(dimethylamino)benzene is a molecule that has been shown to inhibit the growth of hamster v79 cells. It also inhibits the synthesis of DNA and RNA. The binding constants for this molecule have been determined to be 1.0 x 10^9 M^-1, with an n-octanol/water partition coefficient (log P) of 5.5. This molecule is soluble in nonpolar solvents and may be used as a model system for hydrogen bonding interactions or reaction mechanisms in organic chemistry. This compound contains a deuterium isotope and can be used to study the effects of hydrogen bonding on reactions in organic chemistry at high temperatures, with the use of preparative hplc.</p>

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<p>R-(-)-3-Chloro-1,2-propanediol is a chiral epoxide that is used in the synthesis of other chemicals. It has been shown to be active against bacterial strains such as corynebacterium and coryneform bacteria. This chemical can be synthesized from hydrochloric acid and chlorinated propane with an asymmetric synthesis. The R-(-)-3-Chloro-1,2-propanediol can also be synthesized through electrochemical methods using chloride ion as the reducing agent. This compound is soluble in water and shows kinetic activity with carbon sources when used as an antibiotic.</p>