Building Blocks

<p>2,4-Dibromopyridine is a brominated derivative of pyridine. It is synthesized through the substitution of two bromine atoms for two hydrogens on the pyridine ring. This synthesis can be achieved by disubstitution or cross-coupling reactions. The reaction products are nucleophilic and react with electrophiles to produce substitution products. The reaction mechanism is thought to involve a six-membered transition state, which has been observed using X-ray absorption spectroscopy.</p>

<p>2,4-Dimethyl-3-hydroxypyridine is a hydroxypyridine compound with epoxide. It inhibits cytochrome P450 enzymes and is used as an organic solvent. 2,4-Dimethyl-3-hydroxypyridine is also used in research to study the structure of the pyridine ring and the hydroxyl group.</p>

<p>2,5-Dibromopyridine is a chemical compound that can be used as a coupling agent in palladium-catalyzed cross-coupling reactions. It is used on the surface of metal particles to increase the efficiency of the reaction, and has been shown to react with substrates such as sodium hydroxide solution, sodium carbonate, halides and hydroxides. 2,5-Dibromopyridine also reacts with benzoate to form a palladium complex. 2,5-Dibromopyridine can be used as an oxidant or reductant depending on the type of reaction it is being used in. It has redox potentials at -0.6 volts for oxidation and +0.6 volts for reduction.</p>

<p>3-Chloro-5-iodobenzoic acid methyl ester is a versatile building block that can be used to make many complex compounds, including research chemicals and reagents. 3-Chloro-5-iodobenzoic acid methyl ester is used as an intermediate for the production of speciality chemicals and has many uses in chemical reactions. This compound was previously sold under the CAS number 289039-85-6.</p>

<p>2-Chloro-3-(hydroxymethyl)pyridine is an organic compound that is used as a building block for the synthesis of other heterocycles. This compound can be synthesized from 2-chloronicotinic acid, which is obtained by oxidation of nicotine with sodium hypochlorite in the presence of potassium ion. The reaction proceeds via a cleavage of the C-Cl bond and formation of a pyridine ring. The catalytic process can be performed at room temperature and at atmospheric pressure in a variety of solvents, including water.<br>2-Chloro-3-(hydroxymethyl)pyridine has been shown to have high yields for the preparation of compounds such as 2,4-dichloropyridine and 4,5-dichloropyrimidine. It also has been used in the preparation of pharmaceuticals such as atrial natriuretic factor (ANF).</p>

<p>Veterinary drug, ectoparasiticide</p>

<p>Cucurbit[7]uril is a chemical compound that can be used as a fluorescent probe for protein target. It has been shown to produce significant cytotoxicity against cancer cell lines in vitro. Cucurbit[7]uril also exhibits hydrophobic effects, which bind to the cell nuclei of cancer cells and inhibits DNA replication. The photophysical properties of cucurbit[7]uril are stable under physiological conditions and it can be used in vivo as a styryl dye. This chemical compound is also able to form stable complexes with carbonyl oxygens, making it an interesting candidate for anti-cancer drug development.</p>

<p>Cyclopent-2-en-1-ol is a reactive monomer that can react with chloride and hydroxyl groups. It can also undergo reaction with sodium carbonate to form a cyclic ester. Cyclopent-2-en-1-ol can be converted to an epoxide by the use of acid catalyst. This compound also has the ability to polymerize, forming polymers that are used in rayon production.</p>

<p>Versatile small molecule scaffold</p>

<p>Gamma-L-glutamyl-alpha-naphthylamide is an enzyme that catalyzes the conversion of L-glutamic acid to L-glutamate. It is expressed in red blood cells, human liver, and human serum. Gamma-L-glutamyl-alpha-naphthylamide has been shown to have various specificities for different tissues and isoenzymes. This enzyme also has immunoassay procedures that are used to detect it in tissues or cells. These assays use monoclonal antibodies or solubilized gamma-L-glutamyl-alpha-naphthylamide molecules as detection agents.</p>

<p>Versatile small molecule scaffold</p>

<p>2-(2-Azidoethoxy)acetic Acid is a hydrophobic antibacterial agent that can be used to inhibit bacterial growth by disrupting the cell membrane. It has been shown to inhibit the growth of Staphylococcus aureus and Escherichia coli, which may be due to its ability to bind to the glutathione moiety in the bacterial cell membrane. 2-(2-Azidoethoxy)acetic Acid has been shown to have antimicrobial activity against both Gram-positive and Gram-negative bacteria in vitro. This compound is also able to cross the cell membrane, inhibiting bacterial replication in vivo.</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>(S)-(-)-1-Phenylpropylamine is a compound that can be synthesized by the asymmetric synthesis of 1-phenylethylamine. It is an amine that is used in the production of other compounds and has been shown to be reactive with a number of different compounds. The chemical profile of (S)-(-)-1-Phenylpropylamine consists mainly of aldehydes, amides, amines, and alkylating agents. This chiral molecule can be used for the production of drugs or as a precursor for other chemicals.</p>

<p>8-Chlorotetrazolo[1,5-A]pyrazine is a chlorine-containing compound. It is a heterocyclic aromatic organic compound and an important intermediate in the synthesis of other compounds. 8-Chlorotetrazolo[1,5-A]pyrazine is not found in nature. The elimination of chlorine from 8-chlorotetrazolo[1,5-A]pyrazine produces benzotriazole and the molecule tetrazole. 8-Chlorotetrazolo[1,5-A]pyrazine is used as a raw material for many organic syntheses.</p>

<p>Methyl 5-hexynoate is a synthetic product that can be synthesized from soybean lipoxygenase and hydrogenation reduction. This product has been shown to be a useful synthon for the synthesis of monoclonal antibodies with high binding affinity. The synthetic pathway, which involves cross-coupling and asymmetric synthesis, is outlined in the diagram below. The following are the steps involved in the production of methyl 5-hexynoate: 1) Addition of ethyl bromide to terminal alkynes 2) Addition of hydrochloric acid 3) Reaction with potassium tert-butoxide 4) Hydrogenation reduction 5) Cross-coupling reaction 6) Asymmetric synthesis</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>(2S,6S)-2,6-Dimethylmorpholine is an optically pure compound that can be used to optimize the epoxidase reaction. It belongs to the class of morpholines and has two enantiomers. The (2R,6R)-enantiomer is more active than the (2S,6S)-enantiomer in catalyzing the epoxidase reaction. The temperature optima for both enantiomers are different with the (2R,6R)-enantiomer having a higher optimal temperature than the (2S,6S) enantiomer. This compound can be used as a chiral auxiliary to separate racemic mixtures by focusing on one enantiomer at a time. It can also be used as an analytical method for determining plate number and plate height.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-Bromofuran-2-carbaldehyde is a chemical compound that belongs to the group of carbonyl compounds. It is an acetylated form of 3-bromofuran and its molecular formula is C6H5BrO. This chemical contains a carbonyl group, which reacts with the hydroxyl group in epidermal growth factor (EGF) to produce epidermal growth. 3-Bromofuran-2-carbaldehyde has been shown to be an adrenergic receptor agonist and can be used as a structural formula blocker or hydrochloric acid. The chemical can also be synthesized in acidic conditions using methods such as fluorination, chlorination, and acetylation.</p>

<p>Tert-butyl N-(4-methylphenyl)carbamate is a reusable, efficient method for the synthesis of tert-butyl carbamates from amines and carbon dioxide. This reaction is an example of a C–H bond activation that proceeds through an anion intermediate. The reaction time can be reduced by irradiation to increase the efficiency. Electrons are unpaired during this process, which is modeled with quantum mechanics software. Chloride is used as a catalyst to activate the electron and generate a reactive intermediate. Amine functionalities are added to the molecule in order to give it desired properties. The chloride group can be replaced with other anions such as bromide or iodide, which will also introduce different reactivity patterns.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>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>1H-[1,2,3]Triazolo[4,5-d]pyrimidin-5-amine is a nitro compound that binds to the receptor binding sites of certain inflammatory bowel disease and cancer cells. It also inhibits the production of adenosine in these cells. 1H-[1,2,3]Triazolo[4,5-d]pyrimidin-5-amine has been shown to be effective against bowel disease and cancer by inhibiting cyclic AMP (cAMP) degradation. This drug has also been shown to be an irreversible inhibitor of ischemia reperfusion injury in animal models. 1H-[1,2,3]Triazolo[4,5-d]pyrimidin-5-amine is a nitro compound that binds to the receptor binding sites of certain inflammatory bowel disease and cancer cells. It also inhibits the production of adenosine in these cells. 1H</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>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>Flurbiprofen Related Compound A is a compound that inhibits the activity of serine proteases. It binds to the active site of the enzyme, preventing it from breaking down proteins in the body. Flurbiprofen Related Compound A binds to metal surfaces and is also used as a fluorescent probe for biological research. It has been shown to have optical properties and fluorescence properties, which are amplified by an amplifier.</p>

<p>Versatile small molecule scaffold</p>

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

<p>Please enquire for more information about Tert-butyl N-(8-bromooctyl)carbamate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1,2,3,4-Tetrahydropyridin-4-one is an organic compound that can be synthesized by a cross-coupling reaction between a pyridine and chloroformate. The reaction mechanism involves nucleophilic addition of the amine to the electrophile followed by reductive elimination. This process leads to the formation of a tetrahydroquinoline skeleton with stereoselectivity. Tetrahydropyridin-4-one can also be synthesized from an iminium ion or an activated pyridinium salt. The resulting product will have a different skeleton because it was synthesized through different mechanisms.</p>

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

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

<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>(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>4-Methylenepiperidine hydrochloride is a synthetic, ethylene oxide derivative that is used as an antifungal drug. It is also used in the synthesis of other compounds and as a reagent in organic chemistry. 4-Methylenepiperidine hydrochloride can be synthesized by reacting ethylene with an alkoxide, followed by adding a metal halide such as organolithium reagents to form the desired product. The yield rate of this reaction is high and it is easy to perform on a large scale.</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>Cbznh-PEG3-OH is a pegylation product that belongs to the family of PEG products. It is a derivative of Cbz-NH-PEG5-OH and Cbz-N-PEG5-OH, which are carboxybenzyl amido PEG compounds. Pegylation is the process of attaching polyethylene glycol (PEG) chains to molecules, such as proteins or drugs, to enhance their stability, solubility, and bioavailability. Cbznh-PEG3-OH can be used in various applications, including drug delivery systems, diagnostics, and biotechnology. Its unique chemical structure allows for precise control over the size and properties of the PEG chains, making it a versatile tool in the field of biomedical research.</p>

<p>(S)-2-Methylpiperidine hydrochloride is a synthetic reagent that can be used in asymmetric synthesis. It is a homochiral amide that can be used as a reagent for the efficient preparation of β-unsaturated piperidines. (S)-2-Methylpiperidine hydrochloride can be synthesized from a Grignard reaction with an aldehyde, which is an important chemical reaction in organic chemistry.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1H-Indol-2-ylmethanol is a model compound for the synthesis of bioactive molecules. It is used in biological studies as an inhibitor of chronic lymphocytic leukemia, heart disease, and inflammatory pain. The nitro group on 1H-Indol-2-ylmethanol has been shown to activate various enzymes involved in the inflammatory response. The hydroxy group on 1H-Indol-2-ylmethanol has been shown to inhibit cyclooxygenase (COX) enzymes, which are responsible for the production of prostaglandins that cause inflammation.</p>

<p>6-Hydroxy-1-naphthoic acid is a synthetic carboxylate compound with an analog structure that has been shown to be cytotoxic to cancer cells. It inhibits the activity of protein kinases by binding to ATP, which blocks the phosphorylation of tyrosine residues on proteins. 6-Hydroxy-1-naphthoic acid has been shown to inhibit growth factor receptors and induce apoptosis in tumor cells. The mechanism of action for this drug is believed to be through ring opening and hydrolysis of the naphthalene ring, followed by reaction with p-hydroxybenzoic acid. This results in inhibition of histone deacetylase activity, leading to decreased expression of genes involved in cell proliferation.</p>

<p>2-Hydroxy-3-mercapto-1-propanesulfonic acid sodium salt (2HMP) is a diagnostic agent that can be used for the detection of bacterial infections. The conformational properties of 2HMP are similar to those of ATP, which allows it to bind to the polymerase chain reaction enzyme and initiate an enzymatic reaction. This leads to the production of a signal that can be detected by spectrophotometry or fluorometry. 2HMP has also been shown to have chemokine activity in vitro, but this has not been tested in vivo. 2HMP is a competitive inhibitor of human protein serine proteases, such as trypsin and chymotrypsin, with an IC50 value of approximately 1 μM.</p>

<p>Zinc pyrithione is a chemical compound that can be used as an antifungal agent. It has been shown to have genotoxic activity in vitro and in vivo. Zinc pyrithione binds to the surface of the fungal cell wall and inhibits the synthesis of ergosterol, a component of the fungal cell membrane. This binding prevents the formation of an ergosterol-zinc complex with cytochrome P450 enzymes, which are required for sterol biosynthesis, leading to inhibition of energy metabolism. The model system for zinc pyrithione is a mixture of 1-hydroxypyridine-2-thione (1HP) and zinc ions in water. Some studies have shown that zinc pyrithione can cause long-term toxicity, including glycol ether toxicity, when applied topically on hair or skin. Acute toxicities may include skin irritation or contact dermatitis from shampoos containing this substance.</p>