Building Blocks

<p>3,5-Dihydroxybenzaldehyde (DHBA) is a plant metabolite that is classified as a phenolic compound. It is found in many plants and has important biological functions such as the production of carotenoids or the cleavage of carotenoid to form other compounds. DHBA can be extracted from plant tissue with hydrochloric acid or carbon sources. It has been shown that DHBA inhibits the growth of soil bacteria by binding to amines and thus preventing them from reacting with substrates. This may be due to its ability to act as an electron donor, which could also explain its inhibitory activity on carotenoid cleavage.</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>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>1H,1H,7H-Dodecafluoroheptanol is a perfluorinated compound. It has been shown to be an efficient scavenger of reactive oxygen species (ROS) and to have a protective effect on collagen. The reaction mechanism of 1H,1H,7H-dodecafluoroheptanol is not fully understood. However, it has been shown that the chloride ion plays a key role in the formation of this product from 1H,1H,7F-dodecafluoroheptane. The reaction vessel used in this synthesis is critical because it must be anhydrous to prevent the formation of 1HF3OCl. Magnetic resonance spectroscopy has been used to study the chemical structures of this compound.</p>

<p>Disodium 8-amino-1,3,6-naphthalenetrisulfonate is a fluorescent sensor that can detect albumin in human serum. Disodium 8-amino-1,3,6-naphthalenetrisulfonate selectively detects the molecule albumin in blood with a sensitivity of approximately 1.5 nmol/L and a selectivity of nearly 100%. The fluorescent sensor consists of an immobilized nanometer sized molecule of 8-aminonaphthalene trisulfonic acid on hydrotalcite. The sensor has been shown to be selective for albumin and does not react with other serum proteins such as immunoglobulins or fibrinogen.</p>

<p>3,5-Diiodo-L-tyrosine (3DILT) is an iodinated amino acid that can be used as a marker for human immunodeficiency virus (HIV) infection. It is synthesized by the reaction of 3,5-diiodotyrosine with L-tyrosine in the presence of a metal chelate and dinucleotide phosphate. This reaction proceeds via nucleophilic substitution on the aromatic ring with an iodide ion. The product is then purified to remove unreacted 3,5-diiodotyrosine and the metal chelate. 3DILT reacts with antibodies in a luminescence immunoassay to produce light that can be detected. The detection limit of this assay is 10 pg/mL.</p>

<p>4,6-Dimethoxysalicylaldehyde is a protonated molecule with a cyclohexane ring and 4 hydroxyl groups. Its chemical formula is C6H8O3. The compound has low bioavailability due to the presence of an intramolecular hydrogen bond that causes high redox potential. There are two amines on the aromatic ring which can coordinate with metal ions to form a complex. This compound's structural analysis has been conducted using X-ray crystallography, NMR spectroscopy, and IR spectroscopy. The structure of 4,6-dimethoxysalicylaldehyde is unsymmetrical due to the presence of two asymmetric carbon atoms in the molecule. It forms hydrogen bonds with other molecules due to its hydroxyl group and intramolecular hydrogen bond. Hydrogen bonding interactions occur between this compound and other molecules including water, alcohols, ammonia, amines, and carboxylic acids.</p>

<p>2,4-Dinitrophenylacetic acid is a chemical substance with the potential to inhibit acetylation. It can be used as an antigen and has been detected in environmental chemistry. 2,4-Dinitrophenylacetic acid is produced by the reaction of chemicals that are found in the environment and it can be detected at low concentrations. This compound is able to react with proteins in cells, leading to high cytotoxicity. 2,4-Dinitrophenylacetic acid can also stabilize optical systems.</p>

<p>2,4-Dichloro-3-nitropyridine is a halogenated pyridinium salt that has been shown to inhibit the influenza virus in vitro. This compound is also reactive with nucleophilic groups such as amines, alcohols, and thiols. 2,4-Dichloro-3-nitropyridine has been used for the synthesis of quinoline derivatives that have potential applications in autoimmune diseases or cancer. 2,4-Dichloro-3-nitropyridine has also been found to be an inhibitor of tumor necrosis factor alpha (TNFα) production by LPS stimulated human monocytes.</p>

<p>2,5-Dimethyl-1,4-benzenediamine is an amine that is used as a reagent in organic synthesis. It is also used to derivatize other molecules and as a precursor to other compounds. 2,5-Dimethyl-1,4-benzenediamine has been shown to be a good nucleophile and can react with electrophiles such as difluoride and the metal ion Ag(I). The reaction rate of 2,5-dimethyl-1,4-benzenediamine can be determined using high performance liquid chromatography or electrospray ionization. This compound can be synthesized from phenylmagnesium bromide and methyl iodide in the presence of aluminium chloride. It is possible to immobilize 2,5-dimethyl-1,4-benzenediamine on mesoporous silica by attaching it to the surface of the porous material with aminop</p>

<p>3,5-Dimethylbenzaldehyde is an organic compound that is a colorless liquid. It has a chemical formula of C9H12O2 and is classified as an aldehyde. 3,5-Dimethylbenzaldehyde can be synthesized by the reaction of isopropyl palmitate with xylene in the presence of carbon as a source. The reaction time required for this synthesis is approximately one day. The major products of this reaction are 3,5-dimethylbenzaldehyde and 2-methylbutanal. This reaction mechanism can also be used to determine the concentration of urinary metabolites in human urine samples. Analysis of these samples requires an organic solvent such as hexane or dichloromethane. Kinetic data was collected from the rate at which zinc powder reacts with 3,5-dimethylbenzaldehyde over time at different concentrations. A kinetic experiment was conducted using c–h bond activation to produce 3,5-dimethoxy</p>

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

<p>3,4-Difluoro-1H-Pyrrole is a neutral compound with a molecular weight of 136.17 g/mol. It has the chemical formula C6H3F2N and it can be found in reactions involving the congener and coordination chemistry. 3,4-Difluoro-1H-Pyrrole is an intermediate in organic synthesis that is used as starting material for other organic compounds such as pharmaceuticals and agrochemicals. The redox potential of 3,4-Difluoro-1H-Pyrrole is -0.42 V for the reaction with chloride solution and its basicity is 0.89 mM at 25°C. This molecule has been studied by X-ray crystallography and by titration calorimetry for hydrogen bonding interactions.</p>

<p>Ru(bpz)3[PF6]2 is a catalytic reagent that was developed for the synthesis of indoles. It is composed of a ruthenium complex with two ligands, bpy and pfpz. Ru(bpz)3[PF6]2 can be used to synthesize indoles from simple organic compounds containing benzene rings. Ru(bpz)3[PF6]2 has been used by researchers to synthesize indoles in the laboratory. The catalytic activity of this compound depends on the reaction conditions, including temperature and solvent type. This catalyst has also been shown to be able to generate new types of molecules that are not found in nature.</p>

<p>Versatile small molecule scaffold</p>

<p>2-Ethyl-2-oxazoline is a structural analysis of 2-ethyl-2-oxazoline. It is a biocompatible polymer that has been shown to be cytotoxic to cells in culture. The mechanism for this cytotoxicity is not clear, but it may be due to the significant hydroxyl group present in the molecule. 2-Ethyl-2-oxazoline is also a pharmacological agent and can be used as an adjuvant in vaccines. This polymer has shown no significant antibody response and has water vapor permeability properties.</p>

<p>C3-Ethylbenzoic acid is an organic compound that can be synthesized from the reactants ethyl bromide, propylene oxide, and acetic anhydride. The synthesis of C3-Ethylbenzoic acid is a stepwise process in which the starting materials are converted to intermediates and then reacted to form the desired product. The reaction mechanism involves bond cleavage, which generates a carboxylic acid group on one end of the molecule and a phenyl group on the other end. C3-Ethylbenzoic acid interacts with clausamine and isoprene during transport through cell membranes. This interaction may lead to increased permeability of cell membranes by c3-ethylbenzoic acid.</p>

<p>6-Maleimidocaproic acid N-hydroxysuccinimide ester (6MCA-NHS) is a fluorescent probe that reacts with the hydroxyl group of fatty acids in human serum and other biological samples. 6MCA-NHS binds to the carboxylic acid group at the end of a fatty acid molecule, forming a covalent bond. This process generates light emission that can be detected by a fluorescence probe to measure changes in pH or other chemical properties within the solution. 6MCA-NHS has been used as a tumor treatment, where laser ablation is used to break up tumor cells and release 6MCA-NHS into the cytoplasm. The drug can then bind to DNA molecules and inhibit protein synthesis, which results in cell death.</p>

<p>Please enquire for more information about 2-Methyl-2H-indazol-5-ylamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Methyl 3-bromobenzoate is a cross-coupled compound with three functional groups: a methyl group, an acid bromo group, and a carboxylic acid benzoic ester. It is used in the synthesis of antigens that are chemically reactive to trifluoroacetic acid gas. The clinical studies have shown that the efficiency of this study is low because it has been found to be difficult to synthesize methyl 3-bromobenzoate in large quantities. This molecule can be prepared by the reaction of vinylene with an electrophile in non-polar solvents or by catalytic mechanisms.</p>

<p>(S)-1-N-Boc-2-methylpiperazine is a quinolone synthon that has been shown to have antibacterial activity against bacteria. The synthesis of this compound is done through the condensation of piperazine with an N-Boc protected 2,6-dichloroquinoline. This reaction proceeds in good yield and enantioselectivity. The antibacterial properties of (S)-1-N-Boc-2-methylpiperazine are not yet known.</p>

<p>Please enquire for more information about N-Nitroso ramipril including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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<p>N-Boc-4-piperidineacetaldehyde is a chiral, stable, and readily available aldehyde. It has been used in the synthesis of various biologically active molecules including imidazolidinones, which are important for their use as catalysts in organic chemistry. The synthesis of this molecule by the condensation of 4-piperidineacetic acid with acetaldehyde followed by reduction with sodium borohydride is an example of this type of reaction. N-Boc-4-piperidineacetaldehyde can be used to synthesize imines and linkers that are covalently bonded to the protein backbone. This molecule also has conformational stability and is not susceptible to oxidation or radiation damage.</p>

<p>2-Naphthol-6,8-disulfonic acid is a synthetic organic compound that was identified as an impurity in the glyphosate formulation, Roundup. 2-Naphthol-6,8-disulfonic acid has been shown to have good analytical properties and can be used for the analysis of glyphosate in wastewater samples. It is thermally stable with a melting point of about 220°C. The UV detection wavelength ranges from 220nm to 240nm and the chloride ion is detectable at concentrations greater than 0.1 ppm. 2-Naphthol-6,8-disulfonic acid can also be used for the analysis of fatty acids in plants and animals.</p>

<p>4-Phenyl-piperidine is a nitro compound that has been shown to be toxic for the kidneys and nervous system. 4-Phenyl-piperidine has been shown to inhibit dopamine uptake in the striatum and locomotor activity in rats. It also inhibits the hydrolysis of hydrochloric acid, which produces hydrogen ion (H+) ions, resulting in an acidic environment. The chemical structures of 4-phenyl-piperidine are similar to those of tricyclic antidepressants drugs, such as amitriptyline and imipramine, with a phenyl ring attached to an amine group. This drug is used as a pharmaceutical preparation for treating depression by inhibiting the reuptake of serotonin and norepinephrine, which are neurotransmitters that affect mood.</p>

<p>Potassium 3-(phenylsulfonyl)benzenesulfonate is a chemical compound that is used as an anti-aging agent. It has been shown to reduce the viscosity of acrylonitrile, and is most effective when it is at a concentration of 1%. Potassium 3-(phenylsulfonyl)benzenesulfonate also reduces the strain on polymer fibers, which can be caused by temperatures or deionized water. The optimum temperature for this compound is about 50°C. Potassium 3-(phenylsulfonyl)benzenesulfonate does not have any adverse effects with other chemicals in the production process, and does not react with hexamethylenetetramine or aminopropyl naphthenate. This chemical also has a low cost and high tolerance for additives such as styrene or additives such as resistant</p>

<p>3-Pyridylboronic acid pinacol ester is a versatile reagent that can be used in the synthesis of polymers with reactive functionalities. This compound is a crosslinker, which means that it reacts with two or more other molecules to form a covalent bond. 3-Pyridylboronic acid pinacol ester has been shown to react with ring-opening methacrylate monomers and expand their polymer backbone, which leads to an increase in the number of reactive groups on the chain. The introduction of 3-pyridylboronic acid pinacol ester can also introduce fluorescent units into polymers for use as probes for biological systems. There are many possible applications for this versatile reagent, including its use in the synthesis of imidazopyridine ligands.</p>

<p>Pyrrole-2-carboxylic acid is a polycyclic aromatic compound that can be found in coal tar. It has been shown to have anti-inflammatory, antiallergic, and antifungal properties. Pyrrole-2-carboxylic acid is produced by the human body as an intermediate in the metabolism of tryptophan. This compound can also be synthesized and used to treat chronic bronchitis, which is caused by excessive mucus production and inflammation of the airways. The reaction mechanism for pyrrole-2-carboxylic acid is similar to that of other drugs that are used in respiratory therapy, such as aminophylline or acetylcysteine.</p>

<p>Prop-1-en-2-ylboronic acid is a chemical compound that belongs to the group of aromatic hydrocarbons. It is used in pharmaceutical preparations as a monomer and as a chiral building block for the synthesis of oxazolidinones, which are used in medicinal chemistry as protein inhibitors against cancers. Prop-1-en-2-ylboronic acid is also used as a reagent in preparative high performance liquid chromatography. This chemical has shown maximal response against colorectal carcinoma cells and has been shown to be an inhibitor of cholesterol ester transfer.</p>

<p>8-Quinolinesulfonyl chloride (8QSC) is a quinoline derivative that has been shown to have anticancer activity. 8QSC binds to the receptor site of cells and inhibits the production of amines, which are important for cell growth and proliferation. It also binds to hydrogen bonds, which may be involved in the cytotoxicity observed in pancreatic cancer cells. 8QSC shows significant cytotoxicity against Panc-1 cells, but not against NIH 3T3 cells. This may be due to its ability to form supramolecular aggregates with copper ions and quinoline derivatives.</p>

<p>2,6-Dimethoxyisonicotinic acid is a cytotoxic agent that is structurally related to colchicine and combretastatin A-4. It has been shown to induce apoptosis in cancer cells by inhibiting the polymerization of tubulin. This drug also inhibits the proliferation of cancer cells by binding to DNA and disrupting the synthesis of proteins necessary for cell division. The inhibitory effect on protein synthesis may be due to its ability to inhibit the activity of RNA polymerase II and III, which are essential for transcription. 2,6-Dimethoxyisonicotinic acid also induces an anticancer effect through its ability to bind to phenolic moieties and inhibit the growth of cancer cells.</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>Trans-3-(Benzyloxy)cyclobutanol is a radiolabeled compound that is used as a model system for understanding the metabolism of drugs in humans. It has been shown to be metabolized by the liver to produce metabolites that are excreted in urine. Trans-3-(Benzyloxy)cyclobutanol has also been shown to have tumor cell line stability, which may be due to its ability to inhibit DNA synthesis and protein synthesis in vitro and reduce tumor cells in vivo. Trans-3-(Benzyloxy)cyclobutanol has been shown to have no effect on normal rat plasma and lung carcinoma cells, but does affect prosthetic group activity.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-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>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>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2,5-Diethoxyterephthalohydrazide is an organic compound that has been used for the synthesis of linkers with various functional groups. It is a reactive intermediate in the synthesis of amines and compounds containing amine functional groups. 2,5-Diethoxyterephthalohydrazide has been shown to be stable under environmental conditions and can be used as a linker in organic solvents such as amines, alcohols or esters. This compound has also been shown to exhibit photocatalytic activity when irradiated by UV light. Techniques such as analytical chemistry and techniques can be used to characterize this compound's reactivity and stability.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-Amino-2,6-dimethoxypyrimidine is an organic compound that has been shown to be a methylating agent. It reacts with the hydrogen chloride present in seawater to form methyl chloride and hydrochloric acid. 4-Amino-2,6-dimethoxypyrimidine also interacts with hydrogen bonds and forms hydrogen bonds with other molecules. The molecular modeling study revealed that this compound is soluble in mineral acids such as sulfuric acid and hydrochloric acid. The solubility data also showed that 4-amino-2,6-dimethoxypyrimidine is soluble in water but not in chlorinated water. This drug has shown significant antifungal activity against Cryptococcus neoformans and Gram-negative organisms such as Escherichia coli, Salmonella typhi, Pseudomonas aeruginosa, Klebsiella pneumoniae, Proteus mirabilis, Enterobacter</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>(1R,2S)-2-Phenylcyclopropane-1-carboxylic acid is a dicarboxylic acid that is produced from the decarboxylation of benzyne. This compound has been shown to be a precursor of benzene and ozonolysis. The stereospecifically of (1R,2S)-2-Phenylcyclopropane-1-carboxylic acid has been determined using lead tetraacetate as the substrate. (1R,2S)-2-Phenylcyclopropane-1-carboxylic acid is an asymmetric molecule.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>tert-Butyl 2-bromo-2-methylpropanoate is a versatile compound with various applications. It is commonly used as a cytotoxic agent in the pharmaceutical industry and as an amide intermediate in organic synthesis. This compound has also been studied for its potential therapeutic effects, such as its ability to inhibit the growth of cancer cells. tert-Butyl 2-bromo-2-methylpropanoate is often utilized in research settings to study the efficacy of drugs like rabeprazole and tripterygium. Additionally, it finds applications in the production of polymers, catalysts, and hydrogen atom transfer reactions. With its wide range of uses, tert-Butyl 2-bromo-2-methylpropanoate is a valuable compound for researchers and industries alike.</p>

<p>2,3-Dihydro-1H-pyrrolo[3,2-c]pyridine is an alkaloid compound that has various applications in research and chemical studies. It has been found to interact with dopamine receptors and exhibit photothermal properties. This compound has been studied in the context of G. lucidum (also known as Reishi mushroom) and its potential therapeutic effects. Additionally, it has shown interactions with quinpirole, lithium, ergovaline, efrotomycin, and other compounds. The photocatalytic and fatty acid properties of 2,3-Dihydro-1H-pyrrolo[3,2-c]pyridine make it a versatile compound for various research purposes.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Imidazolidone-4-carboxylic acid is a potent inhibitor of matrix metalloproteinases, which are enzymes that break down proteins in the extracellular matrix. 2-Imidazolidone-4-carboxylic acid inhibits the activity of both serine protease and matrix metalloproteinase, two enzymes involved in the inflammation process. 2-Imidazolidone-4-carboxylic acid has been shown to inhibit the transport of amino acids, leading to decreased protein synthesis and cell growth. It also inhibits cancer cells by disrupting their ability to grow new blood vessels and invade other tissues.</p>

<p>Versatile small molecule scaffold</p>

<p>Hexahydro-1H-pyrrolizin-1-amine is a synthetic compound that is used to control endophytic fungi and fungal diseases in plants. The activity of this molecule is due to the acid molecules that are released when it reacts with plant tissue, which prevents the growth of fungi by inhibiting their cell membranes. Hexahydro-1H-pyrrolizin-1-amine also has an antibacterial effect, which may be due to its ability to bind to bacterial 16S ribosomal RNA and inhibit protein synthesis. This product can be used on plants that are infected with endophytic fungi or fungal diseases. It can also be applied as a preventative measure against future infections.<br><br>The following table summarizes the information for each product:<br><br>Product Name <br>Characteristics <br>Description</p>

<p>Versatile small molecule scaffold</p>

<p>2,6-Dimethylphenylacetic acid is a hydrogen phosphate that is soluble in solvents such as acetonitrile. It has been used in the synthesis of lidocaine with high sensitivity and specificity. It can be used to detect phosphoric compounds, which are often present in pharmaceuticals and food supplements. This compound has also been shown to have a solvent effect on the conditions of the reaction, making it a useful additive for optimizing processes. The main impurities of this compound are 2-methylbenzoic acid and benzoic acid.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Methylthiazole-4-carboxaldehyde is an aldehyde that is the product of the condensation of 2,4-dibenzoylacetone and acetone in the presence of diazomethane. It has been used as a precursor to other compounds such as benzoyl chloride, glyoxal, and aldehydes. 2-Methylthiazole-4-carboxaldehyde can be synthesized using acetylation or nitration of thiols or with glyoxal or aldehyde. The reactivity of this compound is high and can be carried out in high yield.</p>

<p>3-Ethyl-4-methylpyrrole-2,5-dione is a chlorophyll analog. It has been found to be an electron donor in photosystem II of the chlorobium reaction center. The compound was prepared by evaporation of a solution of chlorobenzene and ethyl acetoacetate in carbon tetrachloride with the aid of a vacuum pump. 3-Ethyl-4-methylpyrrole-2,5-dione has also been used as a reagent for the preparation of phycocyanin from Spirulina platensis, which is an important component of blue algae. The compound reacts with phenoxy and furyl groups under acidic conditions to produce carboxylate and calcium carbonate, respectively. Oxidation products are formed in reactions with ethyl group and other organic compounds under alkaline conditions.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about 8-Methylnonan-1-ol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Iridium(III) bis-(2-phenylpyridine) (Ir{dFCF3ppy}2(bpy)) is a monomeric amido ligand that can be used in polymerization processes. It has an average molecular weight of 185.8 and a transition temperature of -55°C. Ir{dFCF3ppy}2(bpy) is soluble in organic solvents such as chloroform and acetone and will react with amines, anionic sites, and cycloalkyl groups to form polymers. The yields of the polymerization process are dependent on the starting materials used.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-Aminopyrrolidin-2-one hcl is an antibiotic that is used to treat tuberculosis. It inhibits the enzyme transacylase, which catalyses the conversion of L-lysine into L-pipecolic acid in bacteria. This antibiotic has been shown to be effective against Mycobacterium tuberculosis and Mycobacterium avium complex. 3-Aminopyrrolidin-2-one hcl has a broad spectrum of activity against gram positive and gram negative bacteria, but it is not active against acid-fast bacteria.</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-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>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>1-Phenyl-1-butanol (1PB) is a chiral compound that forms hydrogen bonds with itself. It is a colorless liquid that is soluble in organic solvents and has a boiling point of 61 °C. 1PB has been found to inhibit the growth of Pseudomonas aeruginosa by inhibiting fatty acid synthesis, which may be due to its ability to inhibit β-hydroxylase activity. 1PB also inhibits the growth of some bacteria (e.g., Staphylococcus aureus) by blocking the synthesis of fatty acids, which are important for bacterial cell membrane integrity. The hydroxyl group in 1PB helps it form hydrogen bonds with other molecules, including proteins and DNA strands, which makes it useful for chromatographic separation and as an antioxidant in food preservation.</p>