Building Blocks

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

2-Bromo-5-iodopyrimidine is a compound that can be used in optical and electronic devices. It is an efficient electron donor for the Suzuki coupling reaction, which is used to synthesize organic compounds. 2-Bromo-5-iodopyrimidine has been shown to have a high quantum efficiency and can be used as an electron acceptor in organic light emitting diodes (OLEDs) and organic field effect transistors (OFETs). It also has been shown to interact with other molecules, such as proteins, sugars, DNA bases, and nucleic acids. The interactions between 2-bromo-5-iodopyrimidine and these moieties are important for the design of molecular architectures that may be useful for fields such as molecular electronics, photonics, nanotechnology, or biochemistry.

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

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

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

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Please enquire for more information about Methyl 6-bromoquinoline-2-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-Morpholinopropylamine is a nitrogen-containing heterocyclic organic amine. It has been shown to bind to receptor cells and inhibit the uptake of chloride ions by liver cells, which may be due to its ability to form hydrogen bonds with chloride ions. The binding constants for this drug have also been determined using X-ray crystallography and nuclear magnetic resonance spectroscopy. 3-Morpholinopropylamine has been shown to have anticancer properties and is able to bind with DNA in a manner that inhibits DNA synthesis. This drug also inhibits the production of hydrochloric acid in the stomach, which may be due to its ability to interact electrochemically with amines.

4-Mercaptobutyric acid is a 3-mercaptopropionic acid, which is an intermediate in the biosynthesis of fatty acids. It is a chemical ligation agent that can be used for the synthesis of polymers and pharmaceuticals. 4-Mercaptobutyric acid can also be used to produce butyrolactone, which has been shown to have anticonvulsant properties. The chemical's photochemical properties make it useful for the production of dyes and fluorescent compounds. 4-Mercaptobutyric acid has been shown to inhibit fatty acid synthesis in Sprague-Dawley rats. The compound also possesses anti-inflammatory properties, which may be due to its ability to inhibit the release of prostaglandin E2 (PGE2) from cells.

5-Methyl-L-norleucine is an amide that is a natriuretic and has been shown to have physiological activities. It has been shown to have restenosis and tumor treatment properties, as well as antimicrobial resistance. 5-Methyl-L-norleucine also acts as a cyclic peptide, which may be due to its disulfide bond. This compound is not only effective in treating microbial infections, but it also has anti-inflammatory properties. 5-Methyl-L-norleucine is found in the genus of plants called "Acorus," so it can be used for plant physiology research.

2-Methyl-2-propanethiol is an electron acceptor and a reagent that can be used for the synthesis of organic compounds. It is soluble in polar solvents, but insoluble in nonpolar solvents. 2-Methyl-2-propanethiol has been shown to react with thiols at concentrations below its optimum concentration. The reaction mechanism is believed to involve adsorption and intramolecular hydrogen transfer. The adsorption process occurs on the surface of the substrate and the intramolecular hydrogen transfer occurs through an intermolecular hydrogen bond with the substrate's hydroxyl group or disulfide bond. When 2-methyl-2-propanethiol reacts with a thiol, it forms a mercaptan group called p2 that contains two substituents, one on each carbon atom. This reaction produces a disulfide bond as well as an electrochemical detector signal known as "activated."

L-Abrine is a plant toxin that belongs to the group of abrinoids. It is a chiral molecule and can exist as an L-form or D-form. The L-form is used in some analytical methods, such as gas chromatography, while the D-form is used in medical purposes. L-Abrine has been shown to have anti-HIV effects by inhibiting reverse transcriptase and deoxyribonuclease activity. It has also been shown to inhibit colony stimulating factor production and decrease bacterial growth in vitro. L-Abrine inhibits the replication of bacteria by binding to adenylate cyclase and blocking the enzyme's ability to synthesize cAMP from ATP. This inhibition prevents protein synthesis, leading to cell death.

Intermediate in the synthesis of edoxaban

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold