Alcohols

Please enquire for more information about 3-Aminomethyl-2-Boc-3,4-dihydro-1H-isoquinoline including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 1-(4-Bromophenyl)-4-methyl-1H-pyrazol-3-ol including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 2-Methoxy-4-nitrophenol potassiumsalt including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-(4-Fluorophenyl)-1,3-thiazole-2-thiol is a compound with diverse pharmacokinetic properties. It has been extensively used in the pharmaceutical industry for its various applications. This compound acts as a steroidal cation and exhibits hydroxylase activity. Additionally, it is known to be a plant metabolite and has been studied for its acid hydroxylase properties. Research Chemicals offers high-quality 4-(4-Fluorophenyl)-1,3-thiazole-2-thiol that has been synthesized using the hydrothermal synthesis method. The crystallography of this compound reveals its unique amide structure and the presence of histidine residues. This compound has gained popularity due to its versatility in different research fields such as medicinal chemistry, drug discovery, and biochemistry. Its ability to interact with glutamate receptors makes it an attractive candidate for studying neurological disorders. Furthermore, 4-(4-Flu

Please enquire for more information about 4-(Aminomethyl)tetrahydro-2H-pyran-4-ol including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-Benzyloxybenzyl alcohol is a condensation product of benzaldehyde and acetone. Hydration leads to the formation of an intramolecular hydrogen bond between the carbonyl group and the hydroxyl group. The ammonium salt is formed by reaction with ammonium chloride in water, which then undergoes a cyclization to form bicyclic ring system. 3-Benzyloxybenzyl alcohol has been shown to have antihistamine properties, as it inhibits histamine release from mast cells.

Please enquire for more information about (2-((4'-Methoxy-[1,1'-bIphenyl]-4-yl)dImethylsIlyl)phenyl)methanol including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Bromo-5-nitrophenol is a chlorinated aromatic compound. It is obtained by the reaction of bromine and nitrophenol, and is a precursor to other compounds. 2-Bromo-5-nitrophenol has been used in the synthesis of many organic compounds, including pyrrole and deuterium isotope effect. The deuterium isotope effect can be detected using proton resonance frequencies in the range of 5 to 8 gigahertz (GHz).

6-Bromoisoquinoline is a tetradentate ligand that can be used as a molecular model to study the binding of metal ions and organic molecules. 6-Bromoisoquinoline has been shown to bind covalently and noncovalently with phosphate groups on the surface of Caco-2 cells and to induce surface-enhanced Raman spectroscopy. This ligand has a high nucleophilicity and reacts readily with chloride, which is an acidic functional group. The reaction products are hydrochloric acid, trifluoroacetic acid, or both. 6-Bromoisoquinoline can also act as an allosteric modulator in some enzymes, such as phosphofructokinase in glycolysis.

Please enquire for more information about [5-(3-Chloro-4-fluorophenyl)-2-furyl]methanol including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about (1-Methyl-1H-pyrazol-5-yl)methanol including the price, delivery time and more detailed product information at the technical inquiry form on this page

5-Hydroxyisoquinoline is a quinoline derivative that is synthesized from aziridine. It has been shown to be a potent insulin sensitizing agent in mice with type 2 diabetes mellitus. 5-Hydroxyisoquinoline has been shown to inhibit the activity of purified enzymes preparations and show high selectivity for chloride channels, which are responsible for the transport of chloride ions across cell membranes. This inhibition leads to an influx of protons into the cell, which may lead to a change in the redox potential and changes in the molecular structure of the molecule. The reaction mechanism involves substitution at position 5 of the isoquinoline ring by hydroxy groups (OH).