Alcohols

Please enquire for more information about 1-(5-Nitro-1H-benzimidazol-2-yl)ethanol including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about N-alpha-Fmoc-Nomega-(2,2,4,6,7-pentamethyldihydrobenzofuran-5-sulfonyl)-D-arginine 4-alkoxybenzyl alcohol resin including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about [3-(2-Chlorophenyl)isoxazol-5-yl]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 6-Chloro-2-thien-2-ylquinoline-4-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 5-(3-Chlorophenyl)-4-[1-(4-chlorophenyl)ethyl]-4H-1,2,4-triazole-3-thiol including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 6,7-Dimethoxy-2-[(4-nitrophenyl)acetyl]-1,2,3,4-tetrahydroisoquinoline including the price, delivery time and more detailed product information at the technical inquiry form on this page

5-Methoxy-1,3,4-thiadiazol-2-ol is a planar molecule with a hydroxyl group on the 5 position and an oxygen atom on the 1,3 and 4 positions. The compound is demethylated to form methylene compounds that are needed for other chemical reactions. Hydride shifts occur intramolecularly between carbon atoms in the ring system. The target compound can be synthesized using asymmetric hydrogenation of 3,4-dimethoxythiadiazole. Spectra obtained from x-rays of this compound show peaks at 2θ = 15.5°, 18°, 20° and 22°. The crystal structure of this substance has been determined as triclinic with space group P1.

Please enquire for more information about 3-(Methoxymethyl)-1H-1,2,4-triazole-5-thiol including the price, delivery time and more detailed product information at the technical inquiry form on this page

17alpha-Hydroxypregnenolone is a steroid hormone that has been shown to have effects on the metabolism of lipids, glucose and protein. This compound is synthesized from progesterone by the enzyme 17alpha-hydroxylase and is converted to 17beta-hydroxyprogesterone by the enzyme 17,20 lyase. It has been shown to have an effect on body mass index in humans and model organisms such as mice. The tissue culture studies showed that 17alpha-Hydroxypregnenolone led to an increase in serum bile acids. In adrenocortical carcinoma cell lines, this compound was found to inhibit the growth of cancer cells through inhibition of DNA synthesis and protein synthesis through inhibition of RNA polymerase II activity. It also inhibits infectious diseases by decreasing virus production and increasing the production of interferon alpha. When synthesized for use in experimental models, this compound can be used as a marker for metabolic disorders or cation

Please enquire for more information about 2-Hydroxyquinoline-4-carbohydrazide 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-Benzyl-1H-benzimidazol-2-yl)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 7-Bromo-3-O-acetyl pregnenolone including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Ethyl 4-oxo-7-(benzyloxy)hydroquinoline-3-carboxylate 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-1,2,3,4-tetrahydronaphthalen-1-ol including the price, delivery time and more detailed product information at the technical inquiry form on this page

Potassium phloroglucinol carboxylate is a fine chemical that can be used as a versatile building block, complex compound, research chemical, reagent, speciality chemical and useful intermediate. It is also a useful scaffold for the synthesis of other compounds. Potassium phloroglucinol carboxylate has been shown to react with a wide variety of functional groups and has been used in the preparation of new compounds. The CAS number for potassium phloroglucinol carboxylate is 91313-55-2.

2-(1H-Indol-1-yl)ethanol is a catalytic amine that was synthesized from ethylene and propylene carbonate. It can be used in the synthesis of 1,2-dihydroquinolinium salts and 1,4-benzoquinone derivatives by reaction with malonates or alcohols. The yield of these reactions increases with longer reaction times. 2-(1H-Indol-1-yl)ethanol has been shown to have a transport mechanism that is anion dependent. This compound has been shown to react with hydrogen bond donors such as hydroxyalkyl groups, which are found on the surface of many substrates. 2-(1H-Indol-1-yl)ethanol has been shown to have potential as an organic solvent for use in electrochemical techniques such as cyclic voltammetry and differential pulse voltammetry.

Please enquire for more information about 3-[(5-Chloro-2-nitrophenyl)amino]propan-1-ol including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-Bromo-1-chloroisoquinoline is a drug substance that belongs to the class of b-raf inhibitors. It is a synthetic, non-proteinaceous molecule that binds to and blocks the activity of the b-raf protein. This binding prevents the activation of downstream signaling cascades, which are necessary for cell proliferation. 4-Bromo-1-chloroisoquinoline is expressed in a variety of mammalian cells, including amine producing cells such as those found in the gut and lungs. The drug has been shown to be an agonist at both CB2 and CXCR4 receptors with chemotactic properties. 4-Bromo-1-chloroisoquinoline has also shown antiinflammatory effects by inhibiting prostaglandin synthesis through its cb2 receptor agonist activity, thereby suppressing inflammation in tissues such as the airways and gastrointestinal tract.

Fmoc-D-phenylalanine 4-alkoxybenzyl alcohol resin is a stable, non-radioactive positron emitting probe for the imaging of receptor agonist binding. It is an affinity label for the detection of bradykinin and other peptides in mouse plasma. Fmoc-D-phenylalanine 4-alkoxybenzyl alcohol resin has been shown to have a biodistribution in mice that is similar to that of the non-targeted probe, BODIPY, and both are taken up by the liver. The emission from this compound is mediated by its electron spin polarization, which can be detected with a positron emission tomography (PET) scanner.

4-Aminophenethyl alcohol is a monosubstituted, basic compound that is used in the laboratory as a cell culture medium supplement to promote growth of fibroblasts. This compound has been shown to stimulate human intestinal cells and human peripheral blood mononuclear cells. 4-Aminophenethyl alcohol acts as a hydroxyl group donor, which may be due to its ability to form hydrogen ions when reacted with sodium hydroxide solution. The reaction of this compound with diazonium salt produces an intermediate, which can be hydrolyzed by the addition of sodium hydroxide solution. The resultant chloride ion reacts with the aminophenethyldihydroxylamine (APDA) moiety to produce APDCl. This product has been shown to increase the population growth rate of fibroblasts in culture by causing DNA synthesis and protein synthesis. Linear regression analysis revealed that there was no statistically significant difference between the control and experimental groups for either DNA

2-Amino-6-methylpyridin-3-ol is an amine that has a thiourea group attached to the nitrogen atom. The dipolar nature of the molecule allows for it to form hydrogen bonds with other molecules in its environment, including potassium ions.

3-Biphenylmethanol is a biphenyl compound that functions as a hydrogen peroxide scavenger. It reacts with hydrogen peroxide to form 3-biphenylmethanal and benzoic acid. 3-Biphenylmethanol can be used in wastewater treatment, where it reduces the amount of hydrogen peroxide by oxidizing naphthalene. This reaction also produces biphenyl and picrate, which are precursors for the synthesis of pyrethroid insecticides. 3-Biphenylmethanol has been shown to catalyze the oxidation of ferredoxin and benzyl esters, which may increase the rate of fatty acid decomposition.

Please enquire for more information about 1,2,3,4-Tetrahydroisoquinoline-7-carbonitrileHydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

Stability -20°C Freezer Applications Useful reagent for preparing amino acid pentachlorophenol active esters. References Kovacs, J., et al.: J. Am. Chem. Soc., 89, 183 (1967)

The (3R,4R)-Pyrrolidine-3,4-diol is a chiral compound that has a hydroxy group, a reactive carbonyl group, and a stereospecific carbonyl group. It is synthesized from the reaction of formaldehyde with aniline and hydrochloric acid. This chemical reacts with hydrogen in the presence of nickel catalyst to form (3S,4S)-pyrrolidine-3,4-diol. The enzyme binding of this compound has been shown to be stereoselective because it binds better to one type of enzyme than another. The kinetic studies have shown that the transfer of this compound is stereospecific because it reacts more readily with one type of enzyme than another.

Please enquire for more information about 4-(4'-Methoxyphenyl)-1-butanol including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 3-Methyl-1H-indazol-7-ol including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-Pyrrolidinol is a chemical compound that belongs to the group of organic compounds with the formula CHNO. It is a colorless liquid that can be prepared by oxidation of 3-hydroxypyridine with hydrogen sulfate. 3-Pyrrolidinol has been used as a cross-linker in biochemistry and as an experimental model protein in studies on enzymatic reactions. It has been shown to react with malic acid, which leads to the formation of 3-pyrrolidinol malonate, a model for the reaction between malonic acid and alcohols. The reaction proceeds via a reversible addition-elimination mechanism and is catalyzed by NAD+/NADH coenzyme system. 3-Pyrrolidinol has also been shown to have anticancer effects against HL60 cells in vitro and may have some potential as an anti-inflammatory agent for cancer treatment.

Please enquire for more information about (3R,5S)-5-(Hydroxymethyl)pyrrolidin-3-ol hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

Timolol is a beta-adrenergic blocker drug that is used to treat glaucoma and other eye diseases. Timolol blocks the action of catecholamines (e.g., adrenaline) on the beta-receptors in the eye, which decreases intraocular pressure. Timolol maleate is available as an ophthalmic solution and tablet for oral use. The most common side effect of timolol is constipation; however, it has been shown to cause bowel disease in some cases. Timolol also has been shown to have mitochondrial functions, inhibiting electron transport, and can have interactions with drugs such as benzalkonium chloride. The pharmacological effects of timolols are dose-dependent and reversible if discontinued. Timolols have been used in combination therapy groups for the treatment of intraocular hypertension or chronic open angle glaucoma in patients who are not responsive to conventional therapy with beta blockers or alpha agonists alone.

Please enquire for more information about 4-Ethyl-5-(3-methylphenyl)-4H-1,2,4-triazole-3-thiol including the price, delivery time and more detailed product information at the technical inquiry form on this page

Dimethylamine reacts with phosphotungstic acid to form a phosphotungstic chloride. This reaction has an optimal reaction time of 24 hours and is carried out in an organic solvent. The product, 6,7-dimethoxy-3,4-dihydroisoquinoline hydrochloride hydrate, is synthesized by reacting the amine with a formylating agent such as oxalyl chloride or methyl chloroformate. The enantiomeric purity can be determined by analyzing the reaction solution using a chiral HPLC column.

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

Please enquire for more information about 4-(Aminomethyl)-1-methyl-3,4-dihydroquinolin-2(1H)-one hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Morpholin-2-ylmethanol hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 7-Chloro-2-(2-methoxyphenyl)-8-methylquinoline-4-carbonyl chloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

7-Methoxyisoquinoline is a methoxy compound with a variety of uses. It can be used as an oral dosage form to treat diabetes, or as a plasticizer in the manufacture of plastics. 7-Methoxyisoquinoline has shown efficacy in treating rheumatoid and arthritis, and is also used to reduce blood sugar levels for people with diabetes. The drug binds to the active site of phosphodiesterase (PDE) type 4 enzyme, which prevents the breakdown of cyclic nucleotides and increases cAMP levels. This leads to increased insulin release from beta cells in the pancreas and decreased glucose uptake by cells. 7-Methoxyisoquinoline also inhibits monolayers of lipids by binding to one side of the bilayer membrane, disrupting its structure and function.

Please enquire for more information about 7-Bromoisoquinoline-3-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 5-[3-(4-Chloro-2-methylphenoxy)propyl]-4-ethyl-4H-1,2,4-triazole-3-thiol including the price, delivery time and more detailed product information at the technical inquiry form on this page

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4-Amino-4H-1,2,4-triazole-3-thiol (ACT) is a carbon disulphide analog that exhibits antimicrobial activity against Trichophyton mentagrophytes, Cryptococcus neoformans, and other fungi. ACT binds to single-stranded DNA and prevents the synthesis of RNA. It also has been shown to inhibit the replication of retroviruses such as HIV. The quinoline derivatives that are used in the synthesis of ACT have been shown to be mutagenic. ACT has also been shown to be active against bacteria such as Staphylococcus aureus and Bacillus subtilis. The activation energies for this compound are β-unsaturated ketones.

Curcumenol is a natural product that has been found to have anti-inflammatory, anti-tumor, and antioxidant effects. It is a yellow crystalline substance that is soluble in water. Curcumenol has been shown to inhibit the production of reactive oxygen species from mitochondria in cancer cells. Curcumenol also inhibits the growth of human breast cancer cells by inducing apoptosis and arresting cancer cell cycle progression, which may be due to its ability to inhibit protein synthesis. This compound has been shown to be effective against infectious diseases such as tuberculosis and HIV as well as cancer tissues.

Please enquire for more information about 2-Amino-4-chloro-5-methylphenol including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Please enquire for more information about N-(8-Hydroxyquinolin-2-yl)acetamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-(4-Methoxyphenyl)propan-2-ol is a synthetic compound that is found in the cannabis plant. It has been shown to have anticancer activity, as well as other medicinal properties. The optical isomers of this compound are nabilone and δ9-THC. The former has been used in the treatment of glaucoma patients, while the latter has shown to produce dysphoria and anxiety. 2-(4-Methoxyphenyl)propan-2-ol also has neurological effects, such as analgesic and anti-inflammatory activities.

Venlafaxine is a selective serotonin and norepinephrine reuptake inhibitor (SNRI) that is used to treat depression. Venlafaxine inhibits the reuptake of serotonin and norepinephrine into the presynaptic neuron, increasing their availability in the synaptic cleft. Venlafaxine has been shown to be effective in treating major depressive disorder and other depressive disorders, such as dysthymia and post-partum depression. The antidepressant effects of venlafaxine are believed to be due to its ability to block the uptake of serotonin and norepinephrine in the brain, resulting in an increased concentration of these neurotransmitters. Venlafaxine is metabolized by CYP2D6, CYP3A4, CYP1A2 and CYP2C19 enzymes, which may result in drug interactions with other drugs metabolized by these enzymes. To control for this effect, venlafaxine blood

Please enquire for more information about Ethyl(E)-7-[2-cyclopropyl-4-(4-flurophenyl)-3-quinolinyl]-5-hydroxy-3-oxo-6-heptenoate 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-(4-Butylphenyl)-6,8-dimethylquinoline-4-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about (4R) -3- (2, 2- Dimethylpropyl) - 1, 2, 4, 6, 7, 8- hexahydro- 4, 7, 7- trimethyl- 4- phenyl-5H- pyrazolo[3, 4- b] quinolin- 5- one including the price, delivery time and more detailed product information at the technical inquiry form on this page

Applications (S)​-​(-​)​-​1-​Phenyl-​1-​propanol is a building block used in the synthesis of inhibitors of steroid 11-β hydroxylation in the adrenal cortex related to androgen production in the fetus. Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package References Zolle, I. et al.: J. med. Chem., 51, 2244 (2008);

2-Methyl-1-butanethiol is a thiol compound that exists in the neutral form. It has been shown to be effective for the formation of a surface film and is used as an additive in polymer synthesis. The crystal structure of 2-methyl-1-butanethiol has been elucidated using X-ray crystallography, revealing a thiolate group with one oxetane ring. This ligand has been optimized for use in chemiluminescent detection, desorption techniques, and structural analysis. It can also be used as a ligand to bind gold nanoparticles to surfaces.

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Please enquire for more information about 5-(1-Benzoylpiperidin-4-yl)-1,3,4-oxadiazol-2-ol including the price, delivery time and more detailed product information at the technical inquiry form on this page