Building Blocks

<p>Applications N,N-Dimethylbenzhydrylamine is a useful research chemical for organic synthesis and other chemical processes.<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 Protiva, M., et al.: Chemicke Listy pro Vedu a Prumysl, 47, 1621 (1953), Blicke, F. F., et al.: J. Am. Chem. Soc., 76, 3161 (1954), Estiu, G. L., et al.: Farmaco, 45, 889 (1990)<br></p>

<p>Applications BENZYL CINNAMATE (cas# 103-41-3) is a useful research chemical.<br></p>

<p>Stability Unstable in acidic solution<br>Applications Trimethyl Orthovalerate is used in the synthesis of dihydropyran-4-ones, via the Maitland-Japp reaction, which can be converted stereoselectively into tetrahydropyran-4-ones. This conversion is useful in the study of the functionalized tetrahydropyran units that are found in the anticancer polyketide lasonolide A and the Civet fragrance which is used in perfumery.<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 Clarke, P., et al.: Org. Biomol. Chem., 13, 4743 (2015)<br></p>

<p>Applications 3,5-Tolylenediamine, is a building block<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></p>

<p>Applications 2,​4-​Diaminoanisole is a component and degredation product of azo dyes in fabrics and textiles. Azo dyes occasionally produce carcinogenic effects and environmental reproductive toxicology. Dyes and metabolites, Environmental TestingEnvironmental toxin on US EPA Toxic Release Inventory list (TRI) list.<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 Nguyen, A. et al.: J. Env. Sci. Health A., 51, 744 (2016);<br></p>

<p>Applications N-(p-Toluenesulfonyl)urea is used in the synthesis of Glyburide (G598350), a second generation sulfonylurea with hypoglycemic activity. Glyburide is an antidiabetic agent.<br>References Hellman, B., et al.: Metabol. Clinc. Experiment., 23, 839 (1974); Tozuka, Z., et al.: J. Pharma. Sci., 100, 4024 (2011);<br></p>

<p>Applications 2-Mercapto-4-methyl-5-thiazoleacetic Acid is used as a reagent for determination of hydroxylamine using fused gold nanoparticles immobilized on sol-gel film modified gold electrode.<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 Kannan, P., John, A.: Anal. Chim. Acta, 663, 158 (2010);<br></p>

<p>Applications Mono-tert-butyl Succinate is a reagent used for the synthesis of fluorinated β2- and β3-amino acids, an inhibitor of α-chymotrypsin.<br>References Peddie, V., et al.: Synthesis, 1845-1859 (2010);<br></p>

<p>Applications A mentha compound showing antimicrobial properties against common bacteria in the food industry such as E.coli and P.aeruginosa as well as strains of yeast.<br>References Tyagi, A.K. et al.: Food. Chem., 137, 108 (2013),Shahmohamadi, R. et al.: Pharmacologyonline., 3, 651 (2011);<br></p>

<p>Applications 3'-Methylacetophenone is a reagent that is used in the preparation of 3-aryl-6-phenylimidazo[2,1-b]thiazoles which has anticancer properties.<br>References Koppireddi, S., et al.: Bioorg. Med. Chem. Lett., 24, 5428 (2014);<br></p>

<p>Applications 5-Azauracil is an antimetabolite.<br>References Jiang, Y., et al.: Bioorg. Chem., 32, 244 (2004), Duraffour, S., et al.: Biochem., 46, 11874 (2007),<br></p>

<p>Applications Octinoxate is used in the preparation of polymer particles for the preparation of UV protective materials.<br>References Steeley, K. et al.: Dyes. Pigments. 105, 12 (2014); Couteau, C. et al.: Pharm. Dev. Tech., 19, 315 (2014); Chem. and Eng. News page 22, Aug. 6 (2018)<br></p>

<p>Applications 1,3-Diacetin is a derivative of Triacetin (T720850) which is used as a food additive and flavorings. Triacetin can be used as an excipient in pharmaceutical products where it is used as a humectant, a plasticizer, and as a solvent. Triacetin can also be used as a fuel additive as an antiknock agent.<br>References Mouret, A., et al.: Green Chem., 16 (1), 269 (2014); Snejdrova, E., et al.: Inter. J. Pharma., 458, 282 (2013)<br></p>