Building Blocks

Versatile small molecule scaffold

<p>5-Nitro-2-piperidinobenzenecarbaldehyde (NPCA) is a synthetic, piperidine substituted aldehyde that can be used as an intermediate in the synthesis of semicarbazide, hydrazine and polyphosphoric acid. NPCA is also an excellent reagent for the production of substituted carbonyls. The substitution pattern on NPCA is dependent on the reaction conditions and substituent groups. NPCA has a conformation that is related to the aromatic ring system. This product has been shown to react with ketones to form substituted piperidines.</p>

<p>3,6-Dichloropyridazine is a chemical compound that belongs to the group of heterocycles. It is used as an intermediate for the production of other chemicals such as pharmaceuticals and pesticides. 3,6-Dichloropyridazine can be used in the treatment of inflammatory diseases by inhibiting cyclic nucleotide phosphodiesterase and preventing the accumulation of cyclic nucleotides. 3,6-Dichloropyridazine has been shown to inhibit cancer cells by binding to α7 nicotinic acetylcholine receptors in the cell membrane. The chlorine atom at position 3 on the pyridine ring is responsible for this effect. In addition, 3,6-dichloropyridazine has been shown to react with both nucleophilic and electrophilic groups. This chemical also displays a wide range of chemical diversity due to its three chlorine atoms.</p>

Docosanol is a drug that is used for the treatment of various skin disorders, including psoriasis, eczema, and ichthyosis. It is also used as an adjuvant in the treatment of chronic obstructive pulmonary disease. Docosanol is a lipid molecule that has been shown to have antiviral, antibacterial, antifungal, and antiprotozoal properties. It can be used as a carrier for topical medications and has been shown to have anti-inflammatory effects. The mechanism of action for docosanol is not well understood but may involve its ability to bind to Toll-like receptors on macrophages and neutrophils in the skin. This binding inhibits the synthesis of inflammatory mediators such as prostaglandins and leukotrienes. Docosanol also has physiological effects on water balance by acting as a surfactant in the lungs and preventing water vapor from escaping through respiratory membranes in the nose or mouth. Docosanol

2,6-Dimethoxyaniline is a synthetic compound that has been used in the past as an antibacterial agent. It has been shown to be effective against Staphylococcus aureus and Escherichia coli, but not against Pseudomonas aeruginosa. 2,6-Dimethoxyaniline forms nanowires with an average diameter of 100 nm and lengths up to 1 micron when exposed to radiation (e.g., gamma rays). The reaction rate is dependent on the architecture and morphology of the azobenzene moiety. The chloride anion coordinates with the nitrogen atom in the molecule, which leads to a phase transition temperature of about 230 K.

2,4-Dibromo-1H-imidazole is a boronate. It is used in the synthesis of heterocyclic compounds. In this process, 2,4-dibromo-1H-imidazole reacts with an alkyl or aryl halide to form a boronic acid that can be coupled with other molecules to form new products. The boronic acids made from 2,4-dibromo-1H-imidazole are versatile intermediates for organic synthesis and can be used as starting materials for the preparation of pharmaceuticals and other useful substances. 2,4-Dibromo-1H-imidazole is also used in Suzuki reactions to form carbon–carbon bonds. This reaction uses palladium as a catalyst to generate new carbon–carbon bonds between two different organic molecules.

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

<p>2,5-Difluoropyridine is a ligand that is used in the synthesis of pharmaceuticals and other organic compounds. 2,5-Difluoropyridine is typically activated by a metal ion (e.g., palladium) to form an organometallic complex. The orientation of substituents on the difluoropyridine ring can affect its reactivity and selectivity. For example, chlorine atoms interact with the electrophilic carbon atom in the ring and orientations with electron withdrawing groups are more reactive than those with electron donating groups. 2,5-Difluoropyridine can be used as a cross-coupling reagent for Grignard reactions and nucleophilic substitution reactions. It also has been shown to inhibit human erythrocyte pyruvate kinase activity in vitro and may be useful for the treatment of diabetic complications such as neuropathy or retinopathy.</p>

3,5-Dichloroaniline is an organic compound that exists in two forms. The form that is of most interest to chemists is the para form, which is also called 3,5-dichloro-4-nitroaniline. It has been shown to be an inhibitor of the P450 enzyme system and can be used as a probe for this enzyme activity. 3,5-Dichloroaniline inhibits the activity of bacterial enzymes such as urease, nitroreductase, and cytochrome C reductase. This compound also inhibits the reaction between hydrochloric acid and ammonia to produce ammonium chloride and water. Solubility data for this compound have been obtained by a variety of methods including in vitro studies and experiments on Sprague-Dawley rats.

<p>4,6-Dichloroisatin is a pro-apoptotic compound that is synthesized from amino acids. It has been shown to have anticancer activity in human liver cancer cells, which may be due to its ability to induce apoptosis. 4,6-Dichloroisatin has also been shown to inhibit the production of electron transport chain proteins in the mitochondria by binding to their regulatory sites and inhibiting their phosphorylation. This inhibition of electron transport chain proteins leads to an accumulation of electrons that can react with molecular oxygen and produce reactive oxygen species (ROS). ROS are known for their ability to cause DNA damage and cell death through oxidative stress.</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold