6-membered Rings

Applications Thiane, is a organic sulfide, that has shown to have antioxidant activity. 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 Chao, Q., et al.: Thermochimica Acta, 447 (2006);

2,4,6-Trimethylbromobenzene is a chemical compound with the molecular formula C7H8Br3. It is synthesized by the reaction of 2,4,6-trimethylaniline and bromine in the presence of a base such as potassium carbonate or sodium hydroxide. The synthesis can be carried out with or without solvent. When heated at reflux in toluene, it undergoes an electrophilic substitution reaction with chloroform to form 2-chloro-6-methylbenzene. 2,4,6-Trimethylbromobenzene can also be synthesized by reacting 1,3-dibromopropane with hydroquinone and dibutyltin dichloride in the presence of a strong acid catalyst. The light emission from this compound appears as a yellow color in solution. The molecule has three asymmetric centers: two on the benz

Applications 4-GUANIDINOBENZOIC ACID METHANESULFONATE (cas# 148720-07-4) is a useful research chemical.

Trimethyl 1,3,5-benzene tricarboxylate is a chemical compound that belongs to the group of polycarboxylic acids. It is used as a polymerization agent in the manufacture of ionic polymers. The first step in this process is cationic polymerization, which involves the reaction between trimethyl 1,3,5-benzene tricarboxylate and sodium citrate to form an ion pair. This process can be followed by hydrolysis with hydrochloric acid and sodium carbonate to release the carboxylate anion from the polymer chain and regenerate trimethyl 1,3,5-benzene tricarboxylate. Trimethyl 1,3,5-benzene tricarboxylate has been shown to have optical properties that depend on its molecular weight and metal surface interactions. It can also be used as a chelating agent for zinc diethyld

Stability Moisture Sensitive Applications Eye irritant. References Bagley, D. M. et al.; Toxicol. In Vitro 13, 505 (1999); Gilleron, L. et al.; Toxicol. In Vitro 11, 641 (1997)

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

Applications 1-(Benzyloxy)-3-[[bis(benzyloxy)phosphoryl]oxy]propan-2-ol is an intermediate in the synthesis of Dihydroxyacetone Phosphate Lithium Salt (D450538), which is a metabolic intermediate involved in involved in a wide variety of metabolic pathways including glycolysis and lipid biosynthesis. In plants, Dihydroxyacetone phosphate is involved with the synthesis of vitamin B6. References Jun Ogawa et. al.: et al.: Bioscience, biotechnology, and biochemistry, 67(4), undefined (2003-6-6); John P Richard, Biochemistry, 51(13), undefined (2012-3-14);

Applications (±)-2-Phenylbutanol is used as a reagent in the synthesis of carbamate derivatives of Felbamate (F231000), as potential anticonvulsant agents. (±)-2-Phenylbutanol is also used to prepare analogs of O-(2-phenylethyl)-N-phenylthiocarbamate which can serve as non-nucleoside HIV-1 reverse transcriptase inhibitors. References Kung, C., et al.: Med. Chem. Res., 19, 498 (2010); Cesarini, S., et al.: Bioorg. Med. Chem., 16, 4173 (2008)

Applications Tetrahydropyran is a useful synthetic intermediate. Tetrahydropyranyl (THP-) ethers derived from the reaction of alcohols and dihydropyran are common intermediates in organic synthesis. In organic synthesis, the 2-tetrahydropyranyl group is used as a protecting group for alcohols. 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 Earl, R., et al.: Org. Synth., 7, 334 (1990); Kluge, A.: Org. Synth., 7, 160 (1990)

3,5-Dihydroxytoluene is a natural compound that is structurally related to p-hydroxybenzoic acid. It has been shown to be an efficient fluorescent probe for the detection of quillaja saponaria in wastewater treatment plants. 3,5-Dihydroxytoluene also reacts with orcinol to produce a disulfide bond and can undergo polymerization reactions with nucleophiles such as amines and thiols. It is not active against aerobacter aerogenes, but has been shown to have high values against carcinoma cell lines.

Applications N-Phenyl-4-biphenylamine (cas# 32228-99-2) is a useful reagent for the preparation of heterocyclic compounds for organic electrical devices. References Oh, H. J., et al.: Repub. Korean Kongkae Taeho Kongbo (2020), KR 2020095104 A

Applications Benzyl 4-Fluorophenyl Ketone is used in the preparation and evaluation of 2,3-diarylpyrazines and quinoxalines as selective COX-2 inhibitors. References Singh, S. et al.: Bioorg. Med. Chem., 12, 1881 (2004);