6-membered Rings

<p>Applications Cyclohexyl phenyl ketone is a useful research chemical in organic synthesis.<br>References Yang, Tonghao, et al.: Org. Let., 20(7), 1875-1879 (2018);Jarava-Barrera, Carlos, et al.: Chem. - A Euro. J., 23(69), 17478-17481 (2017)<br></p>

<p>Applications 4-N,N-Diphenylamino-ß-phenylstilbene (cas# 89114-90-9) is a compound useful in organic synthesis.<br></p>

<p>Applications 3,4-Dimethoxytoluene is a volatile flavor compound found is many substances such as boiled buckwheat flour, wild rice grain and tar of hickory wood smoke.<br>References Yajima, I., et. al.: Agr. Bio. Chem. 47, 729 (1983); Withycombe, D.A., et. al.: J. Agr. Food Chem., 26, 816 (1978); Hruza, D.E., et. al.: J. Agr. Food chem., 22, 123 (1974)<br></p>

<p>Applications trans-1,2-Cyclohexanedicarboxylic Acid is used as a reagent in the synthesis of enantiopure (α-cyanoalkyl)(tetrahydropyrido[4,3-b]indolecarbonyl)cyclohexanecarboxamides and its analogs as selective cathepsin K inhibitors for the treatment of osteoarthritis. Also used as a reagent in the synthesis of novel cyclopentanedicarboxamide sodium channel blockers as a potential treatment for chronic pain.<br>References Dossetter, A.G., et al.: J. Med. Chem., 55, 6363 (2012); Shao, P.P., et al.: Bioorg. Med. Chem. Lett., 15, 1901 (2005)<br></p>

<p>Applications Phenyl Tosylate is an intermediate in synthesizing Diclofenac-13C6 Sodium Salt (D436453), which is a labelled analogue of Diclofenac Sodium Salt (D436450).<br>References Kenny, J. R., et al.: J. Med. Chem., 47, 2816 (2004), Sasaki, A., et al.: J. Pharmacol. Sci., 108, 266 (2008); Dalvie, D., et al.: Chem. Res. Toxicol., 22, 357 (2009)<br></p>

<p>Applications Methyl 2-Amino-3,4,5-trimethoxybenzoate could be a constituent contributing to the aroma of green tea leaves.<br>References Hasegawa, T., et al.: J. Food Eng., 4, 10 (2014)<br></p>

<p>Applications 1,4-Benzodioxan-2-carbonitrile (cas# 1008-92-0) is a compound useful in organic synthesis.<br></p>

<p>Applications Methyl 3-(Hydroxymethyl)benzoate is used in the synthetic preparation of N-acylhydrazone derivatives as lactate dehydrogenase A inhibitors.<br>References Rupiani, S., et al.: J. Med. Chem., 101, 70 (2015)<br></p>

<p>Applications 4-benzylcyclohexan-1-one (cas# 35883-77-3) is a useful research chemical.<br></p>

<p>Applications 5-(Benzyloxy)-2-((benzyloxy)carbonyl)-3-hydroxy-5-oxopentanoic Acid is an intermediate used in the synthesis of 2-[2-[(5-carboxypentyl)amino]-2-oxoethyl]-2-hydroxybutanedioic Acid (C181175), which is derived from Methyl 6-Aminohexanoate Hydrochloride (M287100), which is used as a reagent to synthesize straight chain hydroxamates, compounds that act as inhibitors of Human Histone Deacetylase (HDAC) that have the potential to treat cancer. Methyl 6-aminohexanoate is also sometimes used as a spacer unit for peptide synthesis.<br>References Matthews, S., et al.: J. Chem. Soc. Chem. Commun., 17, 1809 (1995); Remiszewski, S., et al.: J. Med. Chem., 45, 753 (2002)<br></p>

<p>Applications m-Xylene-2,4,6-triol is a reagent used to synthesize a series of flavanone derivatives that show anti-tumor activities.<br>References Shi, L., et al.: Biorgan. Med. Chem. Lett., 20, 5466 (2010)<br></p>

<p>Applications o-Iodochlorobenzene is a building block that has been used as a reactant for the synthesis of biaryl derivatives of seasamol used for their antioxidant activity against DPPH radical.<br>References Rodriguez, S.A., et. al.: Australian J. Chem., 66, 1334 (2013)<br></p>

<p>Stability Light Sensitive, Temperature Sensitive<br>Applications 4-(2-Aminophenyl)-4-oxo-2-butenoic Acid is a novel human lens metabolite from normal and cataractous human lenses. A UV filter.<br>References Mizdrak, J., et al.: Tetrahedron, 63, 4990 (2007); Taylor, L. M., et al.: Exp. Eye Res., 75, 165 (2002)<br></p>

<p>Applications 4'-Hydroxybiphenyl-3-carboxylic Acid is a biaryl compound that can be prepared via palladium bis[(dipiperidinylphosphino)amino]phenyl-catalyzed Suzuki-Miyaura cross coupling reactions of organoboronic acids or trifluoroborates and aryl bromides and can also be synthesized by simultaneous hydroxylation and carboxylation of biphenyls. 4'-Hydroxybiphenyl-3-carboxylic Acid is a useful building block with applications in various syntheses.<br>References Shibahara, F., et al.: Org. Lett., 6, 2437 (2004); Bolliger, J., Frech, C.: Adv. Synth. Catal., 352, 1075 (2010);<br></p>

<p>Applications 3-Hydroxybenzyl Alcohol, is shown to have antioxidant and free radical scavenging activity.<br>References Dhiman, S., et al.: Chemi-Bio. Interac., 182, 119 (2009); Alfaro, C., et al.: Mutation Res., 539(1-2), 187 (2003);<br></p>

<p>Applications DL-3-(Benzylthio)lactic Acid is used in the preparation of somatostatin analogs, affecting growth hormones.<br></p>

<p>Applications Diphenyl Diselenide is an organoselenium compound with pharmacological properties, including antioxidant, glutathione peroxidase-mimetic, and neuroprotective effects. Studies show that Diphenyl Diselenide has demonstrated anxiolytic effects in rodents and can inhibit biofilm formation by Candida albicans, increasing both ROS production and membrane permeability.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Hassan, W., et al.: Eur. J. Pharmacol., 761, 341 (2015); Rosseti, I.B., et al.: J. Trace Elem. Med. Bio., 29, 289 (2015); Ibrahim, M., et al.: Prog. Neuro-Psychoph., 54, 187 (2014)<br></p>

<p>Applications 4-(2-Hydroxy-1,1-dimethylethyl)benzenesulfonamide (cas# 374067-96-6) is a compound useful in organic synthesis.<br>References Morimoto, H., et al.: J. Med. Chem., 44, 3369 (2001),<br></p>

<p>Applications β-oxo-Cyclohexanepropanenitrile is used in the preparation of pyrazoloquinazolinone derivatives as PARP-1 inhibitors. In addition, it is used in the preparation of benzoxazoyl amino cyanopyrimidines which act as negative allosteric mGlu5 modulators. Used in anxiety, depression and addiction treatment.<br>References Orvieto, F. et al.: Bioorg. Med. Chem. Lett., 19, 4196 (2009); Mueller, R. et al.: ChemMedChem., 7, 406 (2012);<br></p>

<p>Applications tert-Butyl N-(Benzyloxy)carbamate has been used in the synthesis of Deferoxamine Mesylate (D228980), an iron chelating agent used in therapy for patients with sickle cell diseases and iron overload. Studies suggest that it can exert potential antioxidant neuroprotective effects in stroke patients<br>References Bergeron RJ, et al. 1992. J Med Chem. Dec 11;35(25):4739-44Inati A, et al. 2010. Am J Hematol. Oct;85(10):782-6 Selim M, et al. 2010. Transl Stroke Res. Mar;1(1):35-9<br></p>

<p>Applications methyl amino(2-bromophenyl)acetate hydrochloride (cas# 1219408-44-2) is a useful research chemical.<br></p>

<p>Applications Ethyl (pentafluorobenzoyl)acetate (cas# 3516-87-8) is a useful research chemical.<br></p>

<p>Applications 7,8-Dihydroxy-3-(4-hydroxy-phenyl)-chromen-4-one (cas# 75187-63-2) is a useful research chemical.<br></p>

<p>Stability Hygrscopic<br>Applications N-(2,6-Dimethylphenyl)-2,2-dichloroacetamide is an intermediate used to prepare Ranolazine (R122500), an antianginal agent.<br>References Aalla, S., et al.: Org. Proc. Res. Dev.,16, 748 (2012)<br></p>

<p>Impurity Xylometazoline EP Impurity D<br>Applications 1-​tert-​Butyl-​3,​5-​dimethylbenzene (Xylometazoline EP Impurity D) is a reagent used in the synthesis of polyarenes as oligonapthalene derivatives as well as in the preparation of arylsulfur trifluorides from diaryl disulfides. Xylometazoline derivative, a vasoconstrictor involved in signal transduction, also used as a nasal decongestant. May be used in treatments involving ischemic injury due to the ability to shift energy metabolism from mitochondrial to glycolysis (2).<br>References 1. Fliri, A. et al.: J. Med. Chem. 2009 Dec 24;52(24):8038-46.2. Gohil, V. et al.: Nat Biotechnol. 2010 Mar;28(3):249-55.<br></p>

<p>Applications 3-Aminomethylbenzoic acid<br></p>

<p>Applications α-Bromo-2,3,4,5,6-pentachlorotoluene is used to prepare trisubstituted symmetrical triazines containing halobenzyl groups as flame retardants.<br>References Herzlinger, A., et al.: Eur. Pat. Appl. (1989), EP 305196 A2 19890301<br></p>

<p>Applications 3-Phosphonobenzoic Acid (cas# 14899-31-1) is a useful research chemical.<br></p>

<p>Applications Methyl 2-Formyl-3-hydroxybenzoate can be used to treat sickle cell disease.<br>References Metcalf, B.W., et.al.: PCT Int. Appl. WO 2020072377 A1, 146, (2020);<br></p>

<p>Applications 2-Amino-4-hydroxybenzoic acid (cas# 38160-63-3) is a useful research chemical.<br></p>

<p>Applications 4-phenylcyclohexanamine (cas# 19992-45-1) is a useful research chemical.<br></p>

<p>Applications Benzyl 6-hydroxyhexanoate is an intermediate in the synthesis of N-5-Carboxypentyl-1-deoxynojirimycin (C181200), which is a ligand used for the preparation of an affinity resin highly specific for glucosidase I purification. Glucosidase I is involved in the post-translational processing of N-linked glycoproteins.<br>References HettKamp, H., et al.: Eur. J. Biochem., 142, 85 (1984); Shailubhai, K., et al.: Biochem. J., 247, 555 (1987); Bause, E., et al.: FEBS, 278, 167 (1991)<br></p>

<p>2-Bromo-1,3,5-triisopropylbenzene is an ethylene acetal that is prepared by the catalyzed reaction of aryl chlorides and anhydrous zinc bromide in the presence of triethylamine. The selectivities of this method are high because it can produce mainly a single isomer. The stereoselectivity is also high because the reaction proceeds with the formation of only one stereoisomer. The mechanism for this reaction involves a nucleophilic substitution of the halogenated aryl chloride with the trialkylborane, which generates two different products. This product has been used in the synthesis of biphenyls and nitro compounds.</p>

<p>p-Toluenesulfonic acid monohydrate is a white, crystalline solid that is soluble in water. It is used as a catalyst for the synthesis of various organic compounds and pharmaceuticals. p-Toluenesulfonic acid monohydrate has been shown to have an effect on the thermal expansion of certain polymers and to be useful for preparation of medicinal preparations with high uptake. This compound can also be used as a carbon source for the production of various organic compounds.</p>

<p>Please enquire for more information about alpha-Hydroxy-alpha-phenylbenzeneacetic acid (3-endo)-8-azabicyclo[3.2.1]oct-3-yl ester hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Bromobenzenesulfonyl chloride is a molecule that can be used to inhibit the uptake of 3-bromobenzoate. The inhibition of uptake is due to the desymmetrization of the unsymmetrical, 3-bromobenzoate. This reaction leads to an increase in the concentration of 3-bromobenzoate. Inhibition studies have shown that 3-bromobenzenesulfonyl chloride has an inhibitory effect on cancer cells and apoptosis pathway. The structural studies have shown that this drug is synthetic and biphenyl can be synthesized from it. T-cell lymphomas have been shown to be inhibited by this drug and heart disease has also been inhibited.</p>

<p>4-Toluenesulfonylmethylisonitrile is a potent antagonist of the malonic acid receptor that has been shown to be reactive. It is synthesized by reacting methyl ketones with trifluoroacetic acid and nitrogen gas in the presence of a catalyst. The reaction mechanism has been studied using gravimetric analysis and the thermodynamic data have been calculated for fatty acids. 4-Toluenesulfonylmethylisonitrile can be used to make esters.</p>

<p>1-Bromo-2-fluoro-3-nitrobenzene is a synthetic chemical that is used as an intermediate in the synthesis of various dyes. It can be obtained by the diazotization of acetyl nitrite and acetonitrile, followed by acetylation with acetic anhydride and hydrolysis with sodium hydroxide. The bromoaniline formed after this reaction is then converted to 1-bromo-2-fluoro-3-nitrobenzene by refluxing it with nitric acid. This chemical can also be synthesized from bromines and chloride in the presence of a diazo salt. It reacts with fluoride or halogens to produce fluorobenzene derivatives, which are used as intermediates for other organic compounds.</p>

<p>Applications 4-Diazobenzenesulfonic acid (cas# 305-80-6) is a useful research chemical.<br></p>

<p>Sodium 4-hydroxybenzenesulfonate dihydrate is a hydrogenated compound with reactive properties. It is used in the production of optical materials and is used to produce hydrogen peroxide, which is a strong oxidizing agent. Sodium 4-hydroxybenzenesulfonate dihydrate has been shown to react with calcium ions to form calcium sulfinates. The luminescence property of this compound can be enhanced by mixing it with other compounds such as x-ray diffraction study, functional groups, or hydrogen peroxide. The reaction time for the formation of sodium 4-hydroxybenzenesulfonate dihydrate can be shortened by adding anions such as sulfamic acid.</p>

<p>4-Chlorobenzenethiol is a chemical compound that contains a fatty acid. It is an intramolecular hydrogen donor with the ability to form a disulfide bond. The compound also has high stability and can be used in organic synthesis reactions involving reactive sulfur groups. 4-Chlorobenzenethiol reacts with sodium carbonate to produce sodium thiocarbonate and chloroform, which are then reacted with phosphorus pentoxide for oxidation. The reaction mechanism is similar to that of the Diels-Alder reaction and the model system involves dinucleotide phosphate. 4-Chlorobenzenethiol can be reacted with hydrochloric acid or trifluoroacetic acid as an oxidizing agent.</p>

<p>1,4-Dicyanobenzene is an organic compound that is used as a reactant in the production of other chemicals. It has been shown to be reactive with nucleophiles such as amines and alcohols. 1,4-Dicyanobenzene has shown good transport properties and can be used in industrial preparation of polymers such as polyurethane. The reaction mechanism for 1,4-dicyanobenzene is nucleophilic attack by a nucleophile on the carbonyl carbon of the double bond. This reaction yields two products: an amide or an aliphatic hydrocarbon. 1,4-Dicyanobenzene can also undergo reactions involving hydrogen bonds with other molecules in order to form new compounds.</p>

<p>4-Acetamidobenzenesulfonyl azide (4ABS) is a low detection reagent that can be used for the determination of 4-acetamidobenzoic acid. It reacts with the amine group in 4-acetamidobenzoic acid to form a sulfonamide intermediate and releases an azide ion. The linear calibration curve was obtained using vibrational spectroscopy and has a detection sensitivity of 0.03 ppm. This method can also be used to determine the functional groups present in dopamine, which have been shown to affect electrochemical impedance spectroscopy measurements.</p>

<p>4-Hydroxybenzenesulfonic acid is a chemical compound that is used as an antimicrobial agent in industrial applications. It is commonly used as a corrosion inhibitor, a chelating agent, and an additive for detergents and other cleaning products. 4-Hydroxybenzenesulfonic acid has been shown to inhibit the growth of bacteria by binding to fatty acids in the cell membrane and preventing them from being incorporated into the cell wall. This process causes the cell wall to weaken and eventually rupture. The reaction mechanism of 4-hydroxybenzenesulfonic acid is similar to that of p-hydroxybenzoic acid, which also inhibits bacterial growth by attacking fatty acids in the cell membrane. 4-Hydroxybenzenesulfonic acid may be preferable because it can be produced from renewable sources rather than from petroleum or natural gas.</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>2,5-Dimethyl-1,4-benzenediamine is an amine that is used as a reagent in organic synthesis. It is also used to derivatize other molecules and as a precursor to other compounds. 2,5-Dimethyl-1,4-benzenediamine has been shown to be a good nucleophile and can react with electrophiles such as difluoride and the metal ion Ag(I). The reaction rate of 2,5-dimethyl-1,4-benzenediamine can be determined using high performance liquid chromatography or electrospray ionization. This compound can be synthesized from phenylmagnesium bromide and methyl iodide in the presence of aluminium chloride. It is possible to immobilize 2,5-dimethyl-1,4-benzenediamine on mesoporous silica by attaching it to the surface of the porous material with aminop</p>

<p>1-Bromo-4-iodobenzene is an aryl halide that can be synthesized by the cross coupling of ethyl formate and hydrochloric acid. This compound is useful in analytical applications, such as chromatographic methods, due to its high solubility in organic solvents. It is also used in synthetic procedures for the preparation of other aryl halides. 1-Bromo-4-iodobenzene has been used to synthesize calcium carbonate via the Suzuki coupling reaction with sodium salts, which are nucleophiles. The carbonyl group on this molecule reacts with the nucleophile, forming an alkyl group and a metal salt. Transfer reactions involving these salts can produce other products with different functional groups.</p>

<p>N-Fluorobenzenesulfonimide is an organic compound with the molecular formula CHFNS. It is a fluorinating agent that can be used for the synthesis of organic compounds. N-Fluorobenzenesulfonimide has been shown to have anti-inflammatory properties and has shown promising results in animal studies for the treatment of hepatitis. The mechanism of action is not fully understood, but it may involve the formation of hydrogen bonds between N-fluorobenzenesulfonimide and amino acid residues in proteins, leading to inhibition of protein synthesis.</p>

<p>1,4-Benzenedicarboxylic acid, monoethyl ester (1,4-BDE) is a monomer that is used in the manufacture of polycarbonates and other plastics. 1,4-BDE is also used as a solvent for xylene and butanol. It has been shown to be useful in the production of polyester fibers. The monomer can be synthesized by reacting ethylene with terephthalic acid or dimethyl terephthalate (DMT). This reaction produces 1,4-BDE and methanol as byproducts. The process is carried out at temperatures of 250 °C to 300 °C and under atmospheric pressure. The purified product can be isolated using distillation or extraction with organic solvents such as benzene or butanol. The reaction can be carried out in the presence of ruthenium, which acts as a catalyst.</p>

<p>2-Oxo-2-(2,4,6-trihydroxyphenyl)acetic acid is a useful synthetic building block/scaffold.</p>