Building Blocks

<p>Applications n-Pentacosane-d52 (CAS# 121578-13-0) is a useful isotopically labeled research compound.<br></p>

<p>Applications 7-Methoxy-4-methylcoumarin (cas# 2555-28-4) is a compound useful in organic synthesis.<br></p>

<p>Applications Used as a general reagent in acylation reactions. A byproduct formed in treated waters, and found in marine life.<br> E0<br>References Zuckermann, R.N. et al.; J. Am. Chem. Soc., 115, 10646 (1992); Bull, R., et al.: Toxicol. Appl. Pharmacol., 182, 55 (2002), Mitch, W., et al.: Water Sci. Technol., 2, 191 (2002),<br></p>

<p>Applications Cyanoacetic acid is a dangerous compound that is commonly used as a synthetic intermediate. Cyanoacetic acid has also been found to have teratogenic effects on rat embryos.<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 Simpson, M., et al.: Food Chem. Toxicol., 24, 634 (1986)<br></p>

<p>Applications The calcium salt of L-5-methyltetrahydrofolic acid which belongs to the group of folate vitamins (Vitamin B9, Folacin). It is a coenzymated form of folic acid.<br>References Prinz-Langhebohi, R.: et al., Br. J. Pharmac., 158, 2014 (2009); Wright, A. et al.: Brit, J. Nutrit., 103, 724 (2010);<br></p>

<p>Applications Dansylhydrazine is a fluorescent marker for carbonyl compounds.<br></p>

<p>Applications 5-Hydroxyindole is a hydroxylated indole used as a building block in the preparation of various pharmaceutical compounds such as indole based neurochemicals. 5-Hydroxyindole is a metabolite of Tryptophan (T894800). 5-Hydroxyindole displayed weak inhibitory activity on human melanoma tyrosinase. 5-Hydroxyindole also showed inhibition of serotonin transport by blood platelets.<br>References Yamazaki, Y. et al.: Zeitsch. Naturforsch. C: J. Biosci., 65, 49 (2010); Kay, W.W. et al.: Gen. Pharmacol., 8, 201 (1977); Ghebregzabher, M. et al.: J. Chrom. Biomed. Appl., 222, 191 (1981);<br></p>

<p>Applications 3-Pyridylacetic Acid is a metabolite of Nicotine (N412420). 3-Pyridylacetic Acid is an antilipemic.<br>References Baer, T.A., et al.: J. Med. Chem., 16, 85 (1973); Kyerematen, G. A., et al.: Drug Metab. Dispos., 16, 125 (1988);<br></p>

<p>Stability Light Sensitive<br>Applications Dichlorodinitromethane is a derivative of nitromethane which is used in the preparation of Thermobaric explosives (TBX's).<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 Mohamed, A.K., Mostafa, H.E.: Int. Ann. Conf. ICT, 44th, 14 (2013)<br></p>

<p>Applications (-)-Form is a pyrolysis product of cellulose and cellulose-containing materials including pulp and paper waste products.Known as a pyrolytic product of cellulose, its very useful as a chiral source for synthesizing natural products because of its highly functionalized structure, which contains one chiral center. Used as chiral building block in organic synthesis.<br>References Essig, M.G., et al.: Carbohydr. Res., 156, 225 (1986), Taniguchi, T., et al.: Synlett, 971 (1996),<br></p>

<p>Stability Hygroscopic<br>Applications Used in nucleophilic substitution.<br>References Genicot, C., et al.: Bioorg. Med. Chem. Lett., 13, 437 (2003),<br></p>

<p>Applications (+)-Citronellal is a monoterpene compound that is formed by the metabolism of plants. (+)-Citronellal is a natural insect repellant, and is the main component of citronellal oil. (+)-Citronellal is also used as a starting material in the one pot synthesis of (-)-Menthol (M218875).<br>References Kwon, Y., et al.: Curr. Biol., 20, 1672 (2010); Lenardão, E., et al.: Tetrahedron, 63, 6671 (2007); Milone, C., et al.: Appl. Catal. A-Gen., 199, 239 (2000)<br></p>

<p>Applications 1-Octyne was used as a mechanism-based inhibitor of AlkB (nonheme di-iron alkane monooxygenase).<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 Alonso, H., et al.: Appl. Environ. Microbio., 78, 7946 (2012)<br></p>

<p>Applications 2-Chloro-N-phenylacetamide is used as a reagent in the synthesis of indolylmethylene benzo[h]thiazolo[2,3-b]quinazolinones which exhibit anticancer and antimicrobial activities in vitro.<br>References Gali, R., et al.: Bioorg. Med. Chem. Lett., 24, 4239 (2014)<br></p>