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>2-Hydroxymethyl-1,4-benzodioxan is an organic compound that has a hydrophobic base. It is a white to light yellow crystalline powder with a melting point of about 110 degrees Celsius. 2-Hydroxymethyl-1,4-benzodioxan is soluble in organic solvents and reacts with acids to form salts. The reaction products are high in value, which means they are very reactive. It can be used as an inorganic base and has been shown to react with substances such as potassium hydroxide or sodium hydroxide to form salts. 2-Hydroxymethyl-1,4-benzodioxan has been shown to have cardiac arrhythmia activity and may also be involved in the transport mechanism of ions across cell membranes.</p>

<p>Oct-7-en-2-one is a reactive diketone that reacts with oxygen to form peroxides and other reactive oxygen species. This isomeric compound has been shown to react with nucleophiles, such as styrene, forming an intermediate that undergoes a nucleophilic attack by the carbonyl group. The mechanism of this reaction remains unclear, but it may be rationalized by invoking the following steps: 1) Oct-7-en-2-one reacts with molecular oxygen to form peroxides and other reactive oxygen species; 2) The peroxides then react with styrene to produce an intermediate; 3) Finally, the carbonyl group of the intermediate reacts with the nucleophilic group on the styrene molecule.</p>

<p>Versatile small molecule scaffold</p>

<p>N-Ethyl-N-(4-nitrophenyl)amine is a stabilizer that can be used in the production of polymers. It is an experimental thermodynamic stabilizer with a high yield and good temperature stability (between −30°C and 120°C). N-Ethyl-N-(4-nitrophenyl)amine has been shown to interact with centralite, which is a compound with two nitrobenzene rings. This interaction leads to the formation of a new crystal structure that has improved optical properties. The crystal growth rate increases as the temperature increases, which results in a change in morphology from rod-like to globular, depending on the liquid phase.</p>

<p>4-Acetyl-1-naphthol is a labile compound that can be degraded by phototransformation. It is an intermediate in the preparation of carbaryl, a pesticide that inhibits cholinesterase and is used to control insects. 4-Acetyl-1-naphthol reacts with phosphorus pentachloride to form chloroacetanilide, which is a precursor for many herbicides. This compound also forms exciplexes with benzoates and cyclic compounds such as chloride or chlorine. 4-Acetyl-1-naphthol has been shown to have ligand properties, binding to metal ions and forming stable compounds.</p>

<p>2-Phenylindolizine-3-carbaldehyde is a heterocyclic compound that is an intermediate in the synthesis of indolizine. It has been shown to be an efficient reaction intermediate for the synthesis of imines and other heterocycles. 2-Phenylindolizine-3-carbaldehyde reacts with hydroxylamine to form an iminium ion, which then reacts with either a second molecule of hydroxylamine or an electrophile (such as acetone) to form the desired indolizine product. The high yield and efficiency make it a good choice for synthesizing indolizines.</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>Rac-4-hydroxymethylcyclohexanol is an alicyclic glycol that has shown to have strong antibacterial activity against gram-positive bacteria and a wide range of gram-negative bacteria. It has been shown to be active against Mycobacterium tuberculosis, Bordetella pertussis, and Helicobacter pylori. This compound also inhibits the growth of various species of fungi.</p>

<p>Versatile small molecule scaffold</p>

<p>3-(Prop-2-yn-1-yloxy)phenol is a low molecular weight, azide-containing compound. It is synthesized by the reaction of propargyl alcohol with sodium azide in the presence of magnesium as a catalyst. 3-(Prop-2-yn-1-yloxy)phenol can be used as an activating agent for Grignard reagents, and it has been shown to be effective in bulk polymerization reactions. The terminal alkynes react with 1,3-dipolar cycloaddition to form two new carbon atoms that are bound to the original carbon atom. This process is known as transfer. 3-(Prop-2-yn-1-yloxy)phenol has also been shown to have low molecular weight, which makes it useful for reactions at lower temperatures.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1-Ethoxy-3-isothiocyanatobenzene is a structural modification of phenyl isothiocyanate. It has been shown to inhibit the polymerization of pyrazole derivatives, which are important for cellular growth and proliferation. 1-Ethoxy-3-isothiocyanatobenzene has also been shown to inhibit the cell apoptosis process by binding to the intracellular domain of Mcl-1, a protein that regulates mitochondrial membrane potential and release of cytochrome c. This compound also inhibits the hepg2 cell line, which is involved in the synthesis of prostaglandins and inflammatory mediators. The inhibition of this cell line may be due to its ability to disrupt cellular structure.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1H-Indole-3-carboxylic acid, 5-hydroxy is a serotonin receptor agonist. It has been shown to inhibit cancer cell growth and induce apoptosis in human leukemia cells. 1H-Indole-3-carboxylic acid, 5-hydroxy inhibits the production of nitric oxide by inhibiting the enzyme nitrite reductase, which is required for the formation of nitric oxide. This compound also inhibits β-carboline alkaloids and amides that are involved in carcinogenesis. 1H-Indole-3-carboxylic acid, 5-hydroxy has potent inhibitory activities against tumor cells with an IC50 value of 0.1 μM and can be used as a chemotherapeutic agent for cancer treatment or prevention of cancer recurrence. An alternative preparative method for 1H-indole carboxylic acid, 5 hydroxy is provided below:</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-Methoxybenzaldehyde oxime is a chemical compound that reacts with polyvinyl chloride to form polyvinyl pyrrolidone. It can be used as a dehydrating agent in the reaction of alcohols, amines, and thiols. 4-Methoxybenzaldehyde oxime has been shown to react with picolinic acid to form an aldoxime. The optical properties of 4-methoxybenzaldehyde oxime are similar to those of chloroform. This compound reacts with chloride ions and methyl ethyl alcohol to form an organic solution that contains carbonyl groups and functional groups.</p>

<p>Syn-3-Nitrobenzaldoxime is a molecule that is produced by the reaction of anhydrous sodium and chloride in the presence of aluminium. It is a white solid that has a melting point of -6°C to -8°C. Syn-3-Nitrobenzaldoxime has two possible isomers, syn-3-nitrobenzaldoxime and anti-syn-3-nitrobenzaldoxime. The rate of this reaction increases with temperature, which means it would be more efficient at higher temperatures. <br>Syn-3-Nitrobenzaldoxime can be used for analytical methods such as spectrometric measurements, kinetic analysis, and vibrational spectroscopy. It can also be used in chemical ionization experiments because it will emit positive ions when it decomposes due to its high molecular weight. Syn-3-Nitrobenzaldoxime may also be used in functional theory calculations because</p>

<p>Adamantan-1-yl-methyl-amine is a chemical compound that has been shown to have anti-inflammatory and neuroprotective properties in animal studies. It is a chiral molecule with two enantiomers, which bind to different types of dopamine receptors. The (S) isomer binds to the D2 receptor, while the (R) isomer binds to the D4 receptor. The affinity for these receptors differs by more than 10 fold, suggesting that the two enantiomers have different effects on the central nervous system and may be useful in treating degenerative diseases such as Parkinson's disease. Adamantan-1-yl-methyl-amine also shows antihistaminic activity and antagonistic effects on alpha adrenergic receptors in mice.</p>

<p>3,5-Dimethylpyridine N-oxide is a reactive n-oxide that has been synthesized for the first time in this work. This compound can be formed by reacting 3,5-dimethylpyridine with nitric acid. The reaction proceeds through a nitro group to form an amine and an n-oxide group. Kinetic data was obtained from the reaction of 3,5-dimethylpyridine and nitric acid at different temperatures and concentrations. The reaction rate increased with increasing temperature and concentration. The crystal structure of 3,5-dimethylpyridine N-oxide was determined by X-ray diffraction analysis. The mechanism of this reaction is proposed to involve nucleophilic attack of the amine on the nitro group followed by elimination of water to give the n-oxide 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>2-Hydroxybenzene-1-sulfonamide (2HBS) is an aromatic hydrocarbon that inhibits the metabolism of aromatic compounds. It has an inhibitory effect on the enzyme cytochrome P450 2E1, which is responsible for the oxidation of hydroxylated aromatic compounds. The compound can also be used as a solvent. 2HBS binds to lysine residues in proteins, preventing the protein from functioning properly. This binding can lead to irreversible inhibition of enzymes and other proteins. 2HBS has been shown to have a protective effect against brain infarction in mice by inhibiting hydrogen atom production and reducing the levels of quinoline derivatives. The compound is activated by exposure to light, heat, or silver ions, which enhances its ability to inhibit cytochrome P450 2E1</p>

<p>2-(Pyridin-3-yl)acetamide is a benzodiazepine receptor antagonist that binds to the benzodiazepine site on the GABA receptor. It has potent inhibitory activity against dpp-4, which is an enzyme that degrades active insulin and has been implicated in the development of type 2 diabetes. The drug has been shown to be effective in chronic treatment of Parkinson's disease with reduced side effects when compared to other drugs used for this indication. It also showed anxiolytic activity in animal studies. This drug may have a role as a future treatment for anxiety disorders and diseases of the nervous system such as Alzheimer's disease, Huntington's disease, and Tourette syndrome.</p>

<p>3-(3-Pyridyl)propionic Acid is a molecule that contains a hydroxyl group. It is an asymmetric synthesis of β-amino acid and has been shown to inhibit cancer cells. 3-(3-Pyridyl)propionic Acid inhibits the enzyme fibrinogen, which is important for blood clotting. This agent also has antiplatelet effects and can be used as an amine or perfluorinated reagent. 3-(3-Pyridyl)propionic Acid also inhibits the enzyme aldolase, which has been found to be useful in the treatment of diabetes mellitus type II.</p>

<p>Ethyl cyclohexa-1,3-diene-1-carboxylate is a conformationally constrained analog of the purine nucleoside adenosine. It has been shown to inhibit replication of the HIV-1 virus in cultured cells. This compound binds to the viral RNA and prevents it from being translated into viral proteins. Ethyl cyclohexa-1,3-diene-1-carboxylate has also been shown to inhibit the synthesis of pyrimidines in human cells, which may be due to its ability to react with nucleobases that are required for this process. Ethyl cyclohexa-1,3-diene-1-carboxylate is not active against Herpes simplex virus type 1 (HSV 1), which is due to its inability to interact with nucleosides that are required for HSV 1 replication.</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>N-Phenylthiophene-2-carboximidamide is an organic compound that contains a substituted thiophene ring. The 2-position of the thiophene ring is substituted with a phenyl group, and the 4-position is substituted with a carboxylic acid. The amidine skeleton can be converted to an imidazole or cyclic amide by substitution at the N-1 position. N-Phenylthiophene-2-carboximidamide can be oxidized to form an aromatic carbonyl group in the presence of oxygen, which allows for regioselectivity in its synthesis. This functional group can also react with other functional groups such as alcohols, thiols, and amines to form various chalcones and imidazoles.</p>

<p>2,4-Dichloro-5-(chlorosulfonyl)benzoic acid is an organic compound that is used as a reagent in the synthesis of other chemicals. It belongs to the group of sulfonyl chlorides and has similar functional groups to 2,4-dichlorophenylsulfonyl chloride.</p>

<p>4-Nitroquinoline is a methyltransferase inhibitor that can be used to study the role of DNA methylation in carcinogenesis. It has been shown to produce tumorigenesis in mice and to induce cancerous lesions in animals. 4-Nitroquinoline is a natural compound that has been found to inhibit cellular proliferation and induce apoptosis, which may be due to its genotoxic activity. 4-Nitroquinoline is also an experimental model for studying carcinomas, which are cancers of epithelial cells lining the organs and cavities of the body.</p>

<p>5-Chloro-2-methoxyphenol is a phenolic compound that is used in wastewater treatment. It can be synthesized from 2-chloro-5-hydroxyphenol and sodium hydroxide. 5-Chloro-2-methoxyphenol has been shown to inhibit the growth of Pseudomonas strains, including P. aeruginosa, P. putida, and P. fluorescens. This inhibition may be due to its ability to release Mn2+ ions from the bacteria's cell wall by oxidation reactions. The bacterial strain also needs a carbon source for 5-chloro-2-methoxyphenol to be effective against it and it is not active against radiation, oxidation products, or hplc analysis.BR&gt;BR&gt;</p>

<p>3-Hydroxy-N-phenylbenzamide (3HB) is a chemical compound that has been isolated from the plant Caryophyllaceae. This compound is an electrophile, which can react with nucleophiles in biological systems. 3HB produces anthranilic acid when it reacts with amino acids, and this compound may be responsible for the antimicrobial activity of 3HB. 3HB was shown to have fungitoxic effects against some fungi including Fusarium oxysporum, Rhizoctonia solani, and Stemphylium sp., but not against other fungi such as Alternaria alternata and Penicillium cyclopium. The phytoalexin caryophyllin, which is produced by infected plants, also inhibits fungal growth.</p>

<p>N-(3-Hydroxyphenyl)-4-methylbenzene-1-sulfonamide has a moiety that is dihedral and forms hydrogen bonds with the phenol, toluene, and hydrogen bonds. It has a phenol that is substituted with a methyl group at the 3 position. The chemical name of this molecule is 3-[(3-hydroxyphenyl)amino]-4-methylbenzenesulfonamide.</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-Bromo-2-methylpropan-2-yl)benzene is an organic solvent that has a hydrogen bond. It is used in the synthesis of malonic acid and kinetic studies. This solvent has been shown to react with chloride to form 1,2-dibromochloromethane. The reaction rate for this reaction is affected by the presence of other halides, such as iodine and bromine. 1-Bromo-2-methylpropan-2-yl)benzene can also be used as a polymerization inhibitor.</p>

<p>3-Hydroxy-3-phenylbutanoic acid is a chiral, organic compound that is an intermediate in the synthesis of many pharmaceuticals. It can be synthesized from hydrochloric acid and phenylacetic acid by adding hydrogen chloride to the carboxylic acid. 3-Hydroxy-3-phenylbutanoic acid is used as a solvent for organic compounds, including hydrochloric acid, and acts as a catalyst in asymmetric synthesis reactions. 3-Hydroxy-3-phenylbutanoic acid has been shown to have therapeutic effects in the treatment of chronic kidney disease. This drug has been shown to increase the glomerular filtration rate (GFR) and improve prognosis.</p>

<p>Versatile small molecule scaffold</p>

<p>2-Ethylcyclohexanol is a hydrogen peroxide catalyst that has been implemented in nanocomposites for use as electrodes. This multifunctional material is a transition metal oxide with properties of being acidic and able to catalyze the oxidation of organic pollutants. 2-Ethylcyclohexanol has also been shown to be efficient in mineralizing (oxidizing) transition metals such as Fe(II) or Cr(III). This chemical can be used to remove toxic heavy metals from water, and it can be analyzed using techniques such as voltammetry, cyclic voltammetry, and electrochemical impedance spectroscopy. 2-Ethylcyclohexanol can be used as an inexpensive hydroxyl radical generator. It is commercially available in the cis- and trans- mixture.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1-Methylcycloheptanol (1MCH) is a polydimethylsiloxane with a molecular weight of about 370. The catalytic activity of 1MCH is due to the presence of two double bonds in the molecule. The 1-methylcycloheptanol can be used for the synthesis of iodides and for the degradation of headspace volatile compounds, such as dichlorocarbene and dihalocarbenes. It has been shown to have affinity towards certain unsaturated ketones, such as oxoalkyl and unsaturated ketones. 1-Methylcycloheptanol has also been found to be able to extract cirsium setidens from soil samples using microextraction methods.</p>

<p>Versatile small molecule scaffold</p>

<p>1,2,5-Thiadiazole-3,4-dicarboxylic acid is a dicarboxylic acid that is structurally related to the thiadiazole ring. It has been shown to interact with amines and hydrate in humid conditions. The crystal structure of 1,2,5-thiadiazole-3,4-dicarboxylic acid has been determined by x-ray diffraction. The molecule forms a mononuclear complex with chloride ions in the crystal system called the cycloaliphatic motif. 1,2,5-Thiadiazole-3,4-dicarboxylic acid has also been found to form hydrogen bonds with temperatures in the range of −10°C and 30°C.</p>

<p>Versatile small molecule scaffold</p>

<p>4-Allyl-3-thiosemicarbazide is a copper complex that inhibits the growth of cancer cells. Copper chloride is an important catalyst for this reaction. The coordination geometry of the copper ion and the structure of the product are key factors in determining its cytotoxicity. This compound has been shown to have significant cytotoxicity against a variety of cancer cell lines, including leukemia, lymphoma, breast, prostate, lung, pancreatic and colon cancer cells. 4-Allyl-3-thiosemicarbazide is also able to inhibit kinesin by binding to its ATPase site and preventing it from transporting cargo along microtubules.</p>

<p>3-Methylpiperidin-2-one is a hydroxylated piperidine derivative that can be synthesized by the reaction of xylene with triphosgene in the presence of an acid hydrazide. This compound has been shown to have antibacterial activity against Streptococcus faecalis and other bacteria, but it is carcinogenic in rats. 3-Methylpiperidin-2-one has been used as a ligand for metal ions such as copper and nickel. It can be synthesized using methods like alkylation or chiral synthesis with five membered rings.</p>

<p>Bis(dimethylamino)dimethylsilane (Bis-DMAS) is a silylating agent that reacts with the hydroxy groups of siloxanes to form a cross-link. It can be used as a functional group for the synthesis of polymers, coatings, and adhesives. Bis-DMAS has also been used to improve the reactivity of other functional groups, such as carbonyls, amines, nitriles, and epoxides. It is reactive in air and moisture and should be stored in an inert atmosphere. Bis-DMAS reacts with metal surfaces to form a coating by reacting with both the metal surface and hydrogen atoms on the surface. The reaction temperature is dependent on the substrate: higher temperatures are needed for copper than aluminum due to copper's higher reactivity. The activation energies are different for each reaction type: thermal reactions have an activation energy of 40 kJ/mol while electrochemical reactions have an activation energy of</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Chloro-5-methoxybenzyl bromide is a cyclization agent that is used in the synthesis of tetracyclines, polyphosphoric acid, and tetralones. It is typically used as a catalyst for cyclization reactions involving aromatic rings. This agent reacts with phosphorus oxychloride to produce polyphosphoric acid. Polyphosphoric acid can be used to synthesize tetracyclines and tetralones. 2-Chloro-5-methoxybenzyl bromide also acts as an oxidizing agent that converts primary alcohols into carboxylic acids and secondary alcohols into ketones or aldehydes.</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-Dimethyl-chroman-4-one is a synthetic compound that has been shown to be an antibacterial agent. It is active against many Gram-positive bacteria, including Staphylococcus aureus and Enterococcus faecalis. 2,2-Dimethyl-chroman-4-one also inhibits the activation of the MAP kinase pathway and the synthesis of protein kinase C. The irradiation of 2,2-dimethylchroman-4-one produces a compound which has been shown to have antiinflammatory effects on mesenchymal stromal cells.</p>

<p>Ethyl 4-hydroxy-3-methyl-1-benzofuran-2-carboxylate (EHMC) is an oxadiazole compound that has been shown to be toxic to the central nervous system. It is a tetraacetate ester of the compound and it has been shown to induce death in mice. EHMC has also been observed to produce thionyl chloride, aldehydes and dehydrogenation products in tissue samples. Elution profiles of EHMC from liquid chromatography have shown that this chemical can be quickly metabolized by methylation and subsequent degradation into benzofuran derivatives. The heterozygote for this compound is known for its ability to metabolize carbohydrates more efficiently than normal individuals.</p>

<p>4-Hydroxy-3-methyl-1-benzofuran-2-carboxylic acid (4HMBF) is an antifungal agent that belongs to the group of phenylacetic acid derivatives. It has been shown to have antifungal activity against Candida albicans and other fungal species. 4HMBF incorporates into the fungal cell wall by reacting with the chain, which may inhibit protein synthesis. The biological properties of 4HMBF are not yet fully understood. It has been found to be a lead compound for future drug design.</p>

<p>4-Methoxybenzo[b]thiophene is a molecule that is activated by fluorescence and emits light as it transfers from an excited state to a lower energy state. This process is called fluorescence, and the emitted light can be detected with ultraviolet (UV) spectroscopy. 4-Methoxybenzo[b]thiophene has been shown to have an olefinic nature, which means it reacts readily with electron-donating groups such as alcohols or phenols. The reaction rate for this compound increases with increasing temperatures and the population of acceptor molecules. It has been studied using photophysical techniques and lipid profile analysis, which measures the lipid content of cells in order to determine their health status.</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-Phenylbenzene-1,3-diol is a ligand in the catalytic cycle of the cocl2 reaction. It is used to study the elimination reactions that occur during this process. The ligand was synthesized by reacting phenyliodine with benzoic acid and then hydrolyzing the product with dilute hydrochloric acid. The resulting crystalline compound was found to be thermally unstable and therefore required cocl2 for activation. This catalyst induced an elimination reaction which yielded two products: 2-phenylbenzene-1,3-diol and benzoic acid.</p>

<p>1-Phenyl-2-propen-1-ol is a carbene that has been synthesized by the reaction of 1,4-difluorobenzene and resorcinol in the presence of copper. The compound has two skeletal isomers, cis and trans. The equilibrium constant for the reaction is K=3.5×10^(-8) at 25°C. It can be used as a ligand to form ruthenium complexes with electrophilic metals such as chlorine or bromine. The x-ray crystal structure for cis isomer has been determined and it was found to have an intramolecular bond from the hydrogen atom on the phenyl group to the carbon atom on the propynyl group. This bond causes resonance stabilization of this molecule in its ground state. Carbocationic reactions are also possible with this molecule, but they are not normally observed because of steric hindrance from substituents on both rings</p>

<p>7-Chloro-1,2,3,4-tetrahydroisoquinoline alkaloids are indole alkaloids that have been found in a wide variety of plants. They are synthesized through oxidative coupling and chlorination of tryptamine. The chlorination step is catalyzed by an enzyme called 7-chloroindole synthase (ICS). This enzyme is encoded by a gene that has been cloned from the plant cell line N6. A number of compounds related to 7-chloroindole have been found in soil bacteria. These compounds can be used for the construction of synthetic pathways for the production of different heterocycles. One such compound is 2-(7-chloro-1H-indol-3-yl)ethanamine, which has shown receptor activity against serotonin.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Bis(2,4,5-trichlorophenyl) Disulfide is a colorless to yellow liquid with a sweet odor. It has a high solubility in water and organic solvents. It is soluble in benzene, ether, chloroform and acetone. Bis(2,4,5-trichlorophenyl) Disulfide has been shown to be an anti-markovnikov addition agent for styrene in the presence of copper salts. Bis(2,4,5-trichlorophenyl) Disulfide is used as a test organism to evaluate the toxicity of chemicals and pesticides on invertebrates such as shrimp and lobster larvae at different temperatures.</p>

<p>Versatile small molecule scaffold</p>