Building Blocks

<p>Versatile small molecule scaffold</p>

<p>4-[1-(4-Aminophenyl)-1-methylethyl]-phenol is a processable organic solvent that can be used in temperatures between -20°C and 100°C. It has a transition temperature of -10°C and exhibits an unsymmetrical boiling point distribution. 4-[1-(4-Aminophenyl)-1-methylethyl]-phenol has high viscosity and is catalytic, showing nucleophilic properties with techniques such as catalytic reduction or catalytic hydrogenation. The solvents are also soluble in many other solvents, which makes it useful for diffraction techniques. 4-[1-(4-Aminophenyl)-1-methylethyl]-phenol is soluble in many solvents including water, acetone, and tetrahydrofuran (THF).</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-Aminostilbene is a fluorescent stilbene derivative that is used as a synthetic estrogen. It has been shown to possess anti-inflammatory properties and inhibit the production of reactive oxygen species in target tissues. 4-Aminostilbene also possesses anti-cancer properties and has been shown to be effective against Pseudomonas aeruginosa. The mechanism of action for this compound is thought to be via its ability to react with amines, forming diazonium salts in an organic solution.</p>

<p>3-(Pentafluorosulfanyl)benzoic acid (3PFSA) is a quinoline derivative used as an agrochemical. It is a research chemical that has not been tested for neurotoxicity, but it is suspected to be neurotoxic due to its structural similarity to other neurotoxic substances. 3PFSA has the potential to be an analog of the synthetic drug pentafluorobenzoic acid (5FBBA). The structure of 3PFSA includes a trifluoromethyl group, which is a functional group that can make compounds more permeable in the brain and could contribute to neurotoxicity.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-(Pentafluorosulfanyl)benzoic acid is a benzoic acid derivative that has been synthesized by oxidation of the corresponding aniline. It is used as a starting material for the synthesis of other benzoic acid derivatives, such as 4-fluorobenzoic acid and 4-fluorobenzenesulfonic acid. The compound crystallizes with two molecules in the asymmetric unit, each with one fluorine atom. The molecule has a trigonal planar geometry and contains two sulfonyl groups on the para position of the phenyl ring. The compound has been characterized by X-ray diffraction analysis.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>5-Methoxy-2,3-dimethyl-1H-indole is an indole that is used as a drug. It has anti-inflammatory activity and belongs to the class of intermolecular drugs. It works by inhibiting cyclooxygenase (COX) enzymes, which are involved in the synthesis of prostaglandins. 5-Methoxy-2,3-dimethyl-1H-indole can be found as crystals and has a crystal structure that contains a five membered ring with one double bond and one methyl group on each side of the ring.</p>

<p>5-(2-Chloro-phenyl)-[1,3,4]thiadiazol-2-ylamine is a chemical compound that is a member of the heterocyclic family of compounds. It has been shown to be an excellent catalyst for the condensation reaction between amines and aldehydes or ketones. 5-(2-Chloro-phenyl)-[1,3,4]thiadiazol-2-ylamine has also been found to be an efficient catalyst for the hydrogenation of carboxylic acids. The elemental analysis of this product shows that it is composed of carbon (C), chlorine (Cl), hydrogen (H), and nitrogen (N).</p>

<p>Versatile small molecule scaffold</p>

<p>4-Methyl-2-phenylimidazole is a molecule that has a functional theory. It is used as an inhibitor of corrosion and has been shown to inhibit the activity of magnesium oxide in photoelectron spectroscopy. The molecule has two tautomeric forms, which are the keto form and the enol form. When the molecule is irradiated with light, it absorbs photons and changes into its keto form. Its vibrational modes are also observed in infrared spectroscopy. 4-Methyl-2-phenylimidazole has an activation energy of 6.8 eV and can be classified as stable because it does not decompose at room temperature.</p>

<p>2-(dimethylamino)-2-phenyl-acetonitrile is a chiral, electron-rich reagent that can be used for the synthesis of chiral anions. It is a basic reagent and can react with halides to form alkylating agents. The electron-transfer property of this compound makes it useful in organic synthesis as an intermediate in the alkylation of alcohols and phenols with electrophilic reagents.</p>

<p>Versatile small molecule scaffold</p>

<p>2,4-Dibromo-6-nitroaniline is a nitro compound that has been used in the production of dyes. It is also used as a component in the synthesis of other organic compounds. 2,4-Dibromo-6-nitroaniline can be produced by electrolysis of an acid solution containing radical cations and benzene. The radical cations are formed by proton transfer from the acid to the benzene, followed by electron transfer from benzene to the electrode. This process results in the formation of nitro groups on the benzene ring, which undergoes oxidation to form 2,4-dibromo-6-nitroaniline. The cyclic voltammetry shows that this process occurs via two pathways: one with a fast rate and one with a slow rate. The mechanism for this reaction is not yet known.</p>

<p>Versatile small molecule scaffold</p>

<p>Trimethyl-1,3,5-triazinane-2,4,6-trione is a molecule that belongs to the class of aliphatic hydrocarbons. It is an ester compound that has reactive properties and can be used as a crosslinking agent. Trimethyl-1,3,5-triazinane-2,4,6-trione reacts with calcium carbonate to form trimethylcalcium carbonate. The reactive properties of this molecule are due to the presence of nitrogen atoms and divalent hydrocarbon groups. Trimethyl-1,3,5-triazinane-2,4,6-trione also reacts with fatty acids to produce monocarboxylic acid and fatty acid molecules. Molecular modelling studies have shown that trimethyl-1,3,5-triazinane-2,4,6-trione forms linear molecules. Linear regression analysis has been used to determine</p>

2-Methyl-3,4-dihydro-2H-1-benzothiopyran-4-one is a synthetic compound that is used in the synthesis of thioflavones. It can be prepared by cyclodehydration of acetophenone with chlorides and sulfur. This reagent has been shown to react selectively with nucleophiles such as lithium diisopropylamide and triflic acid at the 2 position of the aromatic ring to form an intramolecular cyclic compound. Cyclodehydration of 2-methylbenzothiophene can also produce this compound.

<p>5-Methyl-4-phenyl-1H-imidazole is an epoxy that is used as a medicine. It is a hardener in the form of ammonium salt and has vasodilating properties. It is used to treat cerebral and vascular diseases, such as hypertension and atherosclerosis. 5-Methyl-4-phenyl-1H-imidazole is toxic for the liver and kidneys when administered orally. This compound also has a high affinity for absorbing certain gases, such as dichlorobenzaldehyde, which may be due to its ability to bind with oxygen molecules.</p>

<p>1-Benzosuberone is an organic compound that is reactive. It has been shown to have inhibitory properties in pharmaceutical preparations. The 1-benzosuberone molecule binds to the active site of the enzyme methyl ketones, which catalyzes the oxidation of methyl ketones to form mcf-7. The binding of 1-benzosuberone inhibits this reaction, reducing the production of mcf-7. This reactive form may also be responsible for significant cytotoxicity and asymmetric synthesis in amines. 1-Benzosuberone has been shown to have receptor activity against cervical cancer cells and antimicrobial agents such as dimethyl fumarate and hydroxyl group.</p>

<p>Versatile small molecule scaffold</p>

<p>2-Methyl-2-phenylpropanamide (2MPPA) is a δ-opioid receptor agonist that has been shown to have anorectic and antinociceptive properties. It also interacts with other protein targets, such as the proton pump, in addition to its interactions with the δ opioid receptor. 2MPPA was also found to be safe when tested on mice, although studies are needed to identify its mechanism of action. A functional theory suggests that 2MPPA may act by binding to the δ opioid receptor, which would lead to a decrease in the release of neurotransmitters such as dopamine and serotonin. This would result in an anti-depressant effect and decreased appetite.</p>

<p>Bicyclo[2.2.2]octane-1,4-diyldimethanol is a new macrocyclic compound that has been shown to have hypotensive effects in animal models. This molecule binds to G protein coupled receptors and activates the ganglionic system. The molecular modelling of this compound has shown that it interacts with the binding site of the receptor, which leads to inhibition of the G protein coupled receptor signaling pathway and activation of the ganglionic system.</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>2-{Bicyclo[2.2.1]hept-5-en-2-yl}acetic acid is a monomer that is able to be encapsulated. This monomer has been shown to have selective functionalities in the polymerization of ethylene and other reactive monomers. It has also been shown to react with chlorine, leading to increased stability in the presence of light and heat, as well as being able to act as a catalyst for polymerization reactions. It can also be used as a fluorescent probe because fluorescence intensity increases upon interaction with biomolecules. 2-{Bicyclo[2.2.1]hept-5-en-2-yl}acetic acid may be effective against cancer cells due to its ability to prevent adipose tissue from accumulating in mice by inhibiting lipogenesis and stimulating lipolysis, or breakdown of fat cells, respectively. It also has been shown to stimulate reconstructive tissue formation by</p>

<p>Versatile small molecule scaffold</p>

<p>2-Phenyl-1,3,4-oxadiazole is a 2-phenyloxazole with an oxygen atom at the 1 position. It is a white crystalline solid that is soluble in water and has antibacterial properties. This chemical can be used as a catalyst for the synthesis of organic compounds. 2-Phenyl-1,3,4-oxadiazole reacts with nitro groups to form oxime derivatives and has been shown to inhibit the growth of fungi such as Candida albicans and Aspergillus niger. 2-Phenyl-1,3,4-oxadiazole can also be used as an antifungal agent against Trichophyton rubrum.<br>2-Phenyl-1,3,4-oxadiazole may be synthesized by reacting phenol with acetone in the presence of nitric acid or sulfuric acid. The structural formula for this compound is</p>

<p>Cyclopent-1-en-1-yl)benzene is an aliphatic hydrocarbon that is a cyclopentyl molecule. It is acidic and reacts with water vapor in the atmosphere to produce an ion-exchange reaction. Cyclopent-1-en-1-yl)benzene has been shown to react with aziridine, which may form ring opening products. This chemical has optical properties that are similar to those of benzene, which can be used as a reference for identification. Cyclopent-1-en-1-yl)benzene is an alicyclic aromatic hydrocarbon and it is an acid catalyst for chemical reactions like esterification and saponification. Cyclopent-1-en-1-yl)benzene also has enantiomer, which means that the molecules have different shapes when they rotate around their axis.</p>

<p>Decahydro-2-naphthol is an organic compound that belongs to the group of aromatic compounds. It has two isomers, known as 2,6-decahydronaphthalene and 2,7-decahydronaphthalene. Decahydro-2-naphthol can be obtained by the oxidation of decahydronaphthalene with an oxidation catalyst, such as platinum dioxide. The risk group for this substance is unknown. Decahydro-2-naphthol has anticancer activity as it binds to the carbonyl group on DNA and inhibits nucleic acid synthesis by inhibiting the enzyme ribonucleotide reductase. This substance also has been shown to have a rate enhancement effect on chemical reactions such as substrate binding when mixed with other substances in a ternary complex.</p>

<p>1-Benzothiophene 1,1-dioxide is a potential drug target for the treatment of cryptococcus neoformans. It inhibits bacterial growth by inhibiting the transport properties of the bacteria, which in turn leads to cell death. This compound has been shown to have potent antitumor activity and may be activated through x-ray diffraction data analysis. The compound also has fluorescence properties and hydrogen bond formation, which may aid in its chemical structure.</p>

<p>Versatile small molecule scaffold</p>

<p>Cyclopentylidenecyclopentan-1-one is a synthetic chemical with bioactive properties. It is a predictable and reliable reagent for the synthesis of Grignard reagents and x-ray structures. It can be used as a starting material to synthesize unsaturated ketones through thermal isomerization, which leads to reaction time and transfer reactions.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Methyl-2,3-dihydro-1H-indene is a synthetic compound that has been shown to have hypolipidemic effects in animal models. It has been found to stimulate the activity of phosphatase and increase the levels of isoeugenol in plasma. 2-Methyl-2,3-dihydro-1H-indene also has hepatotoxic effects and can cause nausea, vomiting, and diarrhea when consumed by humans. The chemical is activated by spin resonance and can be used as an insecticide.</p>

<p>Versatile small molecule scaffold</p>

<p>2-Nitrophenol sodium salt is a polymer film that is used for wastewater treatment. It prevents the growth of bacteria by interacting with active substances in the polymer matrix. 2-Nitrophenol sodium salt can also be used as a nutrient solution for plants, such as solanum tuberosum, which is a potato species. The polymer film has been shown to have a pH of 3 and 4, which makes it acidic. When mixed with hydroxide solution, it becomes basic, with a pH of 10 or 11. The interaction between 2-nitrophenol sodium salt and the hydroxide solution creates hydrogen bonding interactions that are necessary to maintain its acidity or basicity.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1-Cyclohexylethanone is an oxidation catalyst for organic substrates. It has been shown to be a potent inhibitor of the synthesis of fatty acids, as well as an effective agent against Mycobacterium tuberculosis and other bacteria. 1-Cyclohexylethanone has been shown to have a high affinity for the lipid bilayer in membranes, where it forms a reversible covalent bond with the hydroxyl group on the fatty acid chain. It also has receptor activity with ferroelectric materials that may make it useful in biological sensors and drug delivery systems.</p>

<p>2-Bromo-5-nitrofuran is a labile, reactive chemical that can be used in a number of different reactions. This chemical has been shown to be an effective antibacterial agent against Gram-positive and Gram-negative bacteria. The mechanism of action for this drug is not well understood, but it may act as a competitive inhibitor of the enzyme protein synthesis by binding to the amine group of amino acids. 2-Bromo-5-nitrofuran has been used in analytical HPLC and is useful in the determination of carbonyl groups.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-(prop-2-yn-1-yl)oxazolidin-2-one is a synthetic compound that is used as a pharmacological tool. The chemical structure of this compound closely resembles that of nucleobases and it has been shown to be a potent antiproliferative agent in cancer cell lines. 3-(prop-2-yn-1-yl)oxazolidin-2-one induces apoptosis through the activation of caspase 3 and 9, which cleaves poly(ADP ribose) polymerase (PARP). This compound also activates the DNA damage response pathway and induces G1 arrest. 3-(prop-2-yn-1-yl)oxazolidin-2-one has shown promising results in preclinical studies on animal models of breast cancer.</p>

<p>2-Methylthiopyrimidine is a pyrimido compound that has been shown to inhibit the growth of herpes simplex virus type-1. The synthesis of this molecule is based on an anthranilic acid derivative, which can be reacted with amines to form 2-methylthiopyrimidine and its isomers. This drug has been shown to react with chloride ions and carbon disulphide in metathesis reactions. 2-Methylthiopyrimidine has a pharmacophore that resembles the structure of nucleosides, which are found in many viruses. The chlorine atoms in the 2-methylthiopyrimidine molecule are positioned in such a way that they can bind to the phosphate groups on the surface of the virus, thereby blocking its ability to replicate.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Cyclohex-2-en-1-ol is a chiral compound with a molecular formula of C8H12O. It has an empirical mass of 114.19 g/mol and a molecular weight of 114.2120 g/mol. Cyclohex-2-en-1-ol is manufactured by the reaction between lactic acid and cyclohexanol in the presence of tartaric acid as a catalyst, which leads to the formation of an amide bond. This chemical reaction can be described by the following equation:</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Methyl 4-methoxypentanoate is an ester with a chemical formula of CH3O(CH2)4CO2. It can be used as a building block for the synthesis of other chemicals. Methyl 4-methoxypentanoate is insoluble in water, and has been shown to form zeolite crystals. This product has been analysed using advances in carbonate chemistry, which provides new knowledge on the catalytic properties of this compound. It has also been synthesized from gamma-valerolactone by catalytic hydrogenation, and is a potential biofuel candidate due to its high carbon content.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Diethyl glutarate is a hydroxyl-containing antimicrobial agent that has been shown to be a strong inhibitor of bacterial growth. It also exhibits strong bactericidal activity against Gram-positive and Gram-negative bacteria. Diethyl glutarate is used in the treatment of microbial infections and was found to be effective against organisms resistant to other antibiotics. It inhibits bacterial growth by reacting with metal ions, forming an insoluble film around the cells that prevents the passage of nutrients into the cell. This process can also lead to the formation of ethylmalonic acid, which is a substrate for mammalian tissue. The use of diethyl glutarate as an antimicrobial agent has potential application in food preservation, especially in meat products such as bacon and ham.</p>

<p>8-Pentadecanone is a light-sensitive, film-forming polymer that undergoes a phase transition from solid to liquid at 26.1°C. The melting point of 8-pentadecanone is 36–38°C and it has a diameter of 0.5 nm. It has been shown to be effective as a light-sensitive coating for the prevention of malonic acid formation in rat liver microsomes and glycol ether degradation in carbonyl group containing compounds such as methyl ethyl acetate and methyl pentanoate. 8-Pentadecanone also has receptor activity, which can be used to detect or quantify other molecules or ions in the sample.</p>

<p>4-Methylheptan-1-ol is an alcohol that is a volatile and monohydric. It is found in the pheromones of insects, such as the triatomine bug, which transmit Chagas disease and also in the volatiles of plants such as cottonseed oil. This chemical has been shown to be an effective insecticide against reduviidae, a group of insects that includes mosquitoes and ticks. 4-Methylheptan-1-ol is also used as a nutritional additive for livestock feed to prevent losses due to insects. This chemical may serve as a chiral building block for the synthesis of other compounds with beneficial properties.</p>

<p>1-Bromopentan-2-one is a chemical compound that has been shown to have significant activity in the prevention of bone loss. It has also been shown to inhibit the cross-linking of collagen, which may be due to its ability to act as an amine scavenger. 1-Bromopentan-2-one is a fluorescent chemical that can be used for research purposes. It has been demonstrated to inhibit the production of lysine and lysine residues when incubated with lysines and amines, which may be due to its ability to act as an amine scavenger. This compound has been shown in model studies to inhibit biochemical reactions such as dicarbonyl formation and protein cross linking.</p>

<p>Versatile small molecule scaffold</p>

<p>Dodecanal is an odorant that can be used as a trifluoroacetic acid (TFA) fluorescence probe. It has been shown to inhibit the growth of human pathogens and human serum, and it also has antimicrobial properties. Dodecanal binds to the hydroxyl group of TFA and forms a covalent bond with the cysteine residues in proteins, inhibiting their function. The optimum concentration for dodecanal is 0.1 mM in human serum. Dodecanal will bind to caproic acid at concentrations of 2 mM or greater, which may affect its fluorescence properties. Dodecanal also binds to CD-1 mice when exposed to concentrations of 1 mM or greater, which may cause some interference with its fluorescence properties.</p>

<p>1-Undecanol is a colorless liquid that is insoluble in water and soluble in organic solvents. It has been shown to be an effective absorption enhancer for the analysis of p-hydroxybenzoic acid with zirconium oxide as a solid phase extraction material. 1-Undecanol has been used as a reaction solution for the polymerase chain reaction (PCR) technique and has been shown to be an effective extractant for fatty acids and hydroxyl groups. It also functions as an antimicrobial agent, cationic surfactant, and polymerase chain reaction enhancer.</p>

<p>1-Decanol is a fatty acid that is soluble in water and has a hydroxyl group. It is used as a raw material for the production of surfactants and other products. 1-Decanol has significant interactions with hydrogen bond, hydrochloric acid, cationic surfactants, biological products, water vapor, and surfaces. The surface methodology for 1-decanol includes surface tension measurements, contact angle measurements, and surface morphology characterization. The hydroxyl group on 1-decanol can react with oxygen or other molecules to form peroxides or other reactive intermediates. Kinetic data for 1-decanol include the rate of reaction with chlorine at various concentrations of hydrogen chloride in an inert atmosphere. Stability data for 1-decanol include thermal expansion coefficients at different temperatures from −10°C to 100°C. Caproic acid is an impurity found in 1-decanol that can form during its production or by degradation during storage.</p>

<p>Methyl 2-octynoate is a chemical that has been shown to bind to the nicotinic acetylcholine receptor. Methyl 2-octynoate has been shown to have antitumor activity in various types of cancer cells, including breast, prostate, and lung cancer cells. This chemical is not known to be chemically stable or film-forming. It also disrupts mitochondrial membrane potential and reduces the endpoints of oxidative phosphorylation. Methyl 2-octynoate was found to have low potency against cancer cells in vitro and in vivo.</p>

<p>Diisobutylamine is an antimicrobial agent that is used in the treatment of infectious diseases. It is a reactive chemical that reacts with inorganic acids to form soluble salts. Diisobutylamine inhibits the production of amines and enzymes, which may lead to the development of autoimmune diseases. Diisobutylamine also has a hydroxyl group and nitrogen atoms, which are essential for its antimicrobial properties. This drug is insoluble in water and polymerizes when heated or exposed to light.</p>

<p>3-Isopropoxy-1-propanol is a molecule that consists of a hydroxyl group, three isopropoxy groups, and a carboxylic acid. It has two functionalities: the hydroxyl group can act as an alcohol, while the carboxylic acid can act as an acid. 3-Isopropoxy-1-propanol can be used in the synthesis of malonic acid with copper (II) chloride. It also has a role in purification of glycol ethers and fatty acids by radiation. This molecule is used as a crosslinking agent for polymeric matrices and it reacts with hydrogen fluoride to form intramolecular hydrogen bonds. 3-Isopropoxy-1-propanol reacts with carbonyl groups to form ketones or esters.</p>

<p>Butyl butyrate is a colorless liquid that has a pleasant odor. It is used in the production of biofuels and as an organic solvent, as well as a flavorant and fragrance. The compound can be found in many fruits such as apples and oranges, where it is responsible for their distinctive smell. Butyl butyrate has been shown to have binding properties with odorants. It reacts with hydrogen fluoride (HF) in the presence of sodium hydroxide (NaOH) to form sodium butyrate, which is used in the manufacture of polyester polymers. Butyl butyrate also participates in the process optimization of polymerase chain reactions by enhancing the efficiency of DNA amplification.</p>

<p>2-[(1-Hydroxypropan-2-yl)oxy]propan-1-ol is a chiral compound that has two enantiomers. The racemic mixture of this molecule is homochiral, meaning that the two enantiomers are not present in equal amounts. The synthetic route to this compound includes the preparation of aminopropanol by reaction with hydrochloric acid followed by addition of ethylene oxide to produce an acetate ester. This synthesis can be accomplished using a preparative scale or on a laboratory scale. The product is then reacted with chlorine gas to produce 2-[(1-hydroxypropan-2-yl)oxy]propan-1-ol as a single diacetate ester, which can be purified by chromatography and finally recrystallized from methanol. This process generates the desired product in high yield and purity.</p>

<p>1,3-divinylbenzene is a monomer that belongs to the group of divinylbenzenes. It is an important polymerization initiator in the production of polyvinyl chloride (PVC). Divinylbenzene is used as a crosslinking agent for vinyl polymers, and can be copolymerized with other monomers such as styrene. This compound has been shown to increase renal blood flow by inhibiting angiotensin II synthesis in rats. 1,3-Divinylbenzene can also be used as a chromatographic stationary phase or as a gelation stabilizer.</p>

<p>4-Methoxy-4-methyl-2-pentanone is a colorless liquid that is soluble in water. The molecule has a boiling point of 177 °C and a density of 0.895 g/mL. This compound has strong UV absorption at 260 nm, which can be used to identify it. 4-Methoxy-4-methyl-2-pentanone is an organic solvent that can be used for pest control as well as for the production of iron oxides and silicon. It also has functional groups such as phenoxy, surfactant, fatty acid, and radiation. 4-Methoxy-4-methyl-2-pentanone can be synthesized by reacting methyl vinyl ketone with methylamine hydrochloride in the presence of iron oxide catalyst.</p>

<p>Trichloroethanol is a chemical compound with the molecular formula CHClCHOH. It is an organic solvent that has been used in the manufacture of lacquers and varnishes, as well as in pharmaceuticals to dissolve resins before making tablets. Trichloroethanol also has been used for therapeutic purposes for the treatment of autoimmune diseases, bowel disease, cancer and metabolic disorders. Trichloroethanol is metabolized by cytochrome P450 enzymes to produce its active form trichloroacetic acid. The metabolites may then bind to DNA, inhibiting RNA synthesis and protein synthesis. This process leads to cell death by apoptosis. Trichloroethanol is also metabolized by glycosidic bond hydrolysis that leads to the formation of a bicyclic heterocycle intermediate which reacts with fatty acids to produce acrolein and other reactive aldehydes that are cytotoxic and can cause oxidative stress in cells.</p>

4,4-Dioxo-1,4-oxathiane is the oxidation product of 1,2,3-trioxane. It has been shown to have a linear range from 0.5 to 5.0 µg/mL with an ionization detector and hydrogen peroxide as the reagent. 4,4-Dioxo-1,4-oxathiane is also capable of detecting sulfide with its photometric assay. A sample containing sodium sulfide will turn the solution yellow due to a reaction between sodium sulfide and hydrogen peroxide in the presence of light. The presence of hyaluronate will cause a decrease in the intensity of coloration at 490 nm due to an increased absorbance at this wavelength. The addition of NaOH will result in a blue color due to a reaction with thioacetals. Agilent offers 4,4-dioxo-1,4-oxathiane as part of their catalog for MS analysis

<p>Methyl hexanoate is a fatty acid that is found in natural oils and fats, such as olive oil. It has a chemical structure of C6H12O2. Methyl hexanoate is used as a model system to study the reactions of organic compounds with hydroxyl groups. The kinetic data obtained from receptor cells show that methyl hexanoate reacts with acyl chains to form methyl myristate, which is an alkane with the molecular formula CH3(CH2)4CO2H. The reaction mechanism for this process includes the following steps: 1) deprotonation of methyl hexanoate by an acid catalyst; 2) elimination of water from the deprotonated molecule; 3) reaction of the resulting carboxylic acid with an acyl chain to produce an ester product; 4) elimination of water from the ester product to form a fatty acid.</p>

<p>2,5-Dimethylmorpholine is an isomeric mixture of two compounds that are related to the morpholine class of chemical compounds. It has been shown to be a good acceptor for styrene and long-chain alkanes. 2,5-Dimethylmorpholine can be used as a mechanistic probe for styrene polymerization reactions, because it yields mechanistic information about the reaction selectivity. It has also been shown to have catalytic properties in amine synthesis and isomers with dodecyl chains.<br>2,5-Dimethylmorpholine is a colorless liquid with a boiling point of 69°C and an odor threshold of 1 ppm.</p>

Ethyl Laurate (Ethyl Dodecanoate) is a glycol ether that is used as a solvent for petroleum products and other organic solvents. It is also used in the manufacturing of polymers and pharmaceuticals. Ethyl Laurate has been shown to inhibit the activity of the receptor in gland cells, which may be due to its ability to form complexes with enzymes or proteins. This compound also inhibits intramolecular hydrogen transfer reactions. The LC-MS/MS method has been used to identify the protein MCL-1 as an ethyl laurate target.

<p>3,7-Dimethyl-1-octanol is a natural compound that is used as a model organism to study the effects of cationic surfactants and detergent compositions on bacteria. It can be found in the odorant binding protein (OBP) of Streptomyces lavendulae where it binds to chlorine atoms. 3,7-Dimethyl-1-octanol has been shown to inhibit bacterial growth by binding to hydroxyl groups and fatty acid chains in proteins. <br>This compound is also used as an ingredient in detergent compositions and glycol ethers. 3,7-Dimethyl-1-octanol has been reported to have a phenolic odor that is likely due to its ability to bind with tryptophan residues at high pH.</p>

<p>Di(2-ethylhexyl)amine is an aliphatic amine that has a high viscosity. It is used as a reactive agent in chemical reactions, a corrosion inhibitor in industry, and as a transport agent in the petroleum industry. Di(2-ethylhexyl)amine reacts with hydroxyl groups to form ester compounds. Di(2-ethylhexyl)amine is also used to extract ethylene diamine from coal tar oils.</p>

<p>Versatile small molecule scaffold</p>

<p>2-Hydroxypropane-1,3-diyl diacetate is a compound that has been studied for use as an antiviral drug. It is a glycol ether and a glycol with the chemical formula CH2OHC(O)CH2CO2H. This compound is an ester of hydroxypropane-1,3-diyl diacetate and zinc powder. The molecular weight of this compound is 254.21 g/mol and its melting point is -7°C to -8°C. It also has a boiling point of 107°C at 760 mm Hg pressure. 2-Hydroxypropane-1,3-diyl diacetate has been shown to inhibit the growth of viruses such as penciclovir and famciclovir in the laboratory, but more research on its effectiveness in humans needs to be done before it can be approved for use in people.</p>

<p>Isopropyl chloroacetate is a reactive carboxylic acid that can be prepared in high yield by the activation of isopropyl alcohol with sodium carbonate. It is an important reagent for organic synthesis, as it reacts with a wide range of functional groups. Isopropyl chloroacetate has been shown to be effective in treating metabolic disorders such as congestive heart failure, as well as being a useful reagent in surface methodology.</p>

<p>3-Methylpentanoic-d11 acid is an organic compound. It is a fatty acid that is produced by the fermentation of yeast. 3-Methylpentanoic-d11 acid can be used as a carbon source for protein synthesis and has been shown to have antifungal activity in vitro against Candida albicans, Saccharomyces cerevisiae, and Aspergillus niger. 3-Methylpentanoic-d11 acid also has radical scavenging activities, which inhibit lipid peroxide formation. This compound does not have any known metabolites or reactions.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>5-Ethyl-2-pipecoline is a sulphanilic compound that is used as a monomer in the production of polystyrene. It is also used in the production of styrene-based plastics and rubber products. This chemical is also used as an intermediate in the synthesis of piperidine and sodamide, which are precursors to pharmaceuticals. 5-Ethyl-2-pipecoline can be polymerized with styrene for use in the manufacture of polystyrene, acrylonitrile, and chloroprene. This chemical has been shown to be a catalyst for the polymerization of ethylene and diphenylmethane.</p>

<p>N,N-Diethyl-1,3-diaminopropane (DEET) is a compound that has been used as an insect repellent. It is a low molecular weight aliphatic amine, with two amino groups and two ethylene diamine groups. The transport properties of DEET are due to its high solubility in aromatic solvents and its lack of reactivity. It is highly soluble in water and glycol ethers. DEET's reaction mechanism begins with the nucleophilic attack of the amine on the carbonyl carbon atom in trifluoroacetic acid, forming an intermediate tautomeric form. The nucleophilic attack by the amine on the carbonyl carbon atom in trifluoroacetic acid leads to a tetrahedral intermediate which undergoes a second nucleophilic attack by hydroxide ion from hydrochloric acid, forming an intermediate tautomeric form. This</p>

<p>3-Chloro-N,N-diethylpropan-1-amine is a reactive molecule that binds to the active site of tuberculostatic activity and is used in chemotherapy. It has been shown to have inhibitory properties against human placental alkaline phosphatase, an enzyme present in large quantities in the placenta. The 3-chloro-N,N-diethylpropan-1-amine is a synthetic compound with antineoplastic properties. It can be used as a chemotherapeutic agent for cancer and gastrocnemius muscle cancer. The molecular structure of 3-chloro-N,N-diethylpropan-1-amine contains oxindole and hydroxyl group.</p>

<p>Versatile small molecule scaffold</p>

<p>(4-Methylphenyl)acetaldehyde is an organic chemical compound that is found in many natural products, including pine oil. This chemical has been shown to be a potent antibacterial agent when it reacts with xylene and amines. (4-Methylphenyl)acetaldehyde has been also shown to react with azides and form carbonyl groups. These reactions are believed to be the key steps in the synthesis of chrysanthenone, a synthetic chemical that has tranquilizing properties. The structure of this compound was first determined by solvents such as benzene, chloroform, and ether.</p>

<p>4-(2-Aminopropyl)phenol is a chemical that is used as a diagnostic and pharmacological agent. It is also known to be a potent inhibitor of dopamine uptake in the brain, and has been shown to affect locomotor activity in a clinical study. 4-(2-Aminopropyl)phenol may be an experimental model for infectious diseases such as malaria, which causes high levels of dopamine release from the central nervous system. It inhibits the oxidation of dopamine by reactive oxygen species (ROS), which prevents the formation of toxic products and protects against oxidative stress.<br>4-(2-Aminopropyl)phenol has been shown to cause death in liver cells by binding with nitrogen atoms, inhibiting cellular respiration through inhibition of cytochrome P450 enzymes.</p>

<p>2-Ethoxy-3,4-dihydro-2H-pyran is a chemical solvent that is used in the manufacture of polymers. It can be used to produce high molecular weight polymers by cationic polymerization. 2-Ethoxy-3,4-dihydro-2H-pyran has been shown to cause cancer in animals and may also be carcinogenic for humans. It has been found to cause chorioallantoic membrane tumors in chickens and bifunctional tumors in rats. Chloride ions are required for the initiation of the polymerization process. The synthetic route to 2-ethoxy-3,4-dihydro-2H pyran involves the reaction of lysine with chloromethyl methyl ether followed by hydrolysis of the ester group. This method is not efficient as it requires an acid catalyst and a metal such as magnesium or calcium or zinc chloride or zinc</p>

<p>N²-Benzyl-N,N-dimethylethylenediamine is a chelating agent that binds metal ions to form a stable complex. It also has the ability to bind to acrylamide and hydrolyze it. This drug is used as an anti-inflammatory, anti-allergic, and anti-diabetic medication. N²-Benzyl-N,N-dimethylethylenediamine has been shown to be safe in humans when used at doses of up to 600 mg/day for 3 months.</p>

<p>1-Phenylsemicarbazide is a triazole antifungal that inhibits the enzyme cytochrome P450, which is required for the synthesis of ergosterol, an essential component of fungal cell membranes. Treatment with 1-phenylsemicarbazide has been shown to increase blood pressure and inhibit the activity of other enzymes in rats. The drug also binds metal ions such as zinc and copper, which may be related to its anti-inflammatory properties. 1-Phenylsemicarbazide binds to receptors in the kidney that are involved in the regulation of salt and water balance, leading to a decrease in urine production. This compound has been shown to inhibit the growth of yeast cells from "Saccharomyces cerevisiae" and "Candida albicans" at concentrations up to 20 mM.</p>

<p>1-(Cyclohexylamino)propan-2-ol is a cleavage product of acetone and pyridine. This compound has been synthesized in Japan by the ring cleavage of 1,2-dichloroethane with sodium azide. The chloride ion reacts with the tosylate group and forms an acylation product. 1-(Cyclohexylamino)propan-2-ol is also a cleavage product of 1,3-cyclohexanedione with sodium azide.</p>

<p>Cinnamic acid is a phenylpropene carboxylic acid and is the parent compound of a group of compounds called cinnamates. It is found in small amounts in many plants, such as cinnamon, and has been used medicinally since ancient times. Cinnamic acid can be synthesized from benzoic acid by means of the Knoevenagel condensation reaction. Cinnamic acid has been shown to have potential anticancer activity, and it also inhibits the enzyme activities of influenza virus neuraminidase and HIV-1 protease. In addition, cinnamic acids are major contributors to the aroma of coffee beans.</p>

<p>3-Phenylpropionamide is a reactive compound that has been shown to have amine and amide functional groups. It is an inhibitor of the enzyme phospholipase A2, which is responsible for the release of arachidonic acid from membrane phospholipids. 3-Phenylpropionamide also blocks the interaction of κ subtype opioid receptors with their ligands and inhibits choroidal neovascularization in animal models. This drug has been shown to be toxic in animals, with adverse effects on metabolic disorders such as gamma-aminobutyric acid (GABA) levels.</p>

<p>3-(Dibutylamino)propylamine is a nitrogen-containing compound that can be used for the treatment of tumors. It has been shown to inhibit the growth of tumor cells in vitro and in vivo by binding to matrix metalloproteinase, a type of enzyme that plays a role in tumor invasion and metastasis. 3-(Dibutylamino)propylamine inhibits tumor cell proliferation by cationic polymerization, which leads to crosslinking between proteins, DNA, and other cellular components. The resulting irreversible damage causes cell death.</p>

<p>2-(Dibutylamino)ethanol is a chemical compound that is used as an analytical reagent for the determination of the magnetic properties of magnetic particles. It can also be used to determine fatty acids in polyethylene glycols and glycol ethers. 2-(Dibutylamino)ethanol has been shown to have anticancer effects in vitro and in vivo, as well as anti-inflammatory properties. It is also used in the synthesis of other pharmaceuticals.</p>

<p>Tripropylamine is an organic compound that belongs to the group of alkylamines. It has a phase transition temperature at -37 °C and can be used as a reagent in chemical synthesis, as well as an intermediate for the production of other compounds. Tripropylamine can be detected by electrochemical impedance spectroscopy (EIS) with a detection sensitivity of 0.5 ppm. Kinetic data for tripropylamine was obtained using methyl ethyl ketone and hydrogen fluoride, which yielded k(M) = 1.2 x 10^-3 and k(S) = 2.4 x 10^-2 M-1s-1 respectively. The reaction mechanism for tripropylamine involves the formation of picolinic acid from 3-hydroxypropionic acid and ammonia, followed by decarboxylation to form picolinic acid.</p>

<p>1,2-Diacetin-d5 is a glycerol derivative that is used as a substrate in the study of mitochondrial and cytosolic calcium levels. It is also used to produce acetate extract, which has been shown to have anti-inflammatory effects in vitro. Acetate extract contains 1,2-diacetin-d5 and other substances that inhibit the activity of epidermal growth factor (EGF). EGF is an important protein for cellular proliferation and migration. 1,2-Diacetin-d5 can be used as a surface methodology for the analysis of proteins on surfaces.</p>

<p>1,3,5-Triethylbenzene is a glycogen synthase inhibitor that has been shown to inhibit the synthesis of glycogen by binding to the anomeric carbon on the type I glycans. A study showed that 1,3,5-triethylbenzene is an efficient method for inhibiting glycogen synthesis in liver cells. The compound binds to mannose residues on the type I glycan and prevents the formation of a glycosidic linkage between two glucose molecules. The binding constants for 1,3,5-triethylbenzene are high and it reacts with active oxygen to form reactive products. This product also forms supramolecular complexes with acid and coordination geometry.</p>

<p>N-Benzyl-N,N'-dimethylethylenediamine is a catalytic agent that is used in the synthesis of organic compounds. It has been shown to have proton and electron densities and to be electron-rich. NBDME has also been shown to react with trichloroacetic acid or trifluoroacetic acid in the presence of riboflavin and oxygen atoms, forming flavoproteins such as isoalloxazine.</p>

<p>Dibenzylethanolamine is a molecule with the molecular formula C17H26O2. It is a dibasic amine, meaning it has two hydroxyl groups. Dibenzylethanolamine has a specific chemical structure that consists of an alcohol group and two amine groups. The hydrogen atoms on the oxygen atoms in the hydroxyl group are replaced by methyl groups. This component is also used as a solvent for organic solutions, such as paints and varnishes.</p>