Building Blocks

<p>Applications (2E)-Decenal is a useful starting material for organic synthesis.<br></p>

<p>Applications 2,2’-Thiodiethanol is a reagent used in the synthesis of water soluble gold-N-heterocyclic carbene complexes for catalytic homogenous acid.<br>References Ibrahim, H. et al.: Adv. Synth. Catal., 357 ,3893 (2015);<br></p>

<p>Applications H-PRO-GLU-OH (cas# 67644-00-2) is a useful research chemical.<br></p>

<p>Applications p-Toluidine Hydrochloride acts as a reagent for the preparation and biological activity of N-acylleucine (arylaminoethyl)amides as non-covalent inhibitors of cathepsin K, L and S. Catalyst in the chemistry of azasteroids.<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 Altmann, E., et al.: J. Med. Chem., 45, 2352 (2002); Vedres, A., et al.: Acta Chimica Academiae Scientiarum Hungaricae, 109, 111 91982)<br></p>

<p>Applications NALPHA-(5-FLUORO-2,4-DINITROPHENYL)-L-LEUCINAMIDE (cas# 178065-29-7) is a useful research chemical.<br></p>

<p>Applications (S)-Pulegone is the stereoisomer of (R)-Pulegone (P840140) which is a monoterpene, commonly found in the essential oils of Nepeta cataria (Catnip).<br>References Sonboli, A., et al.: Chem. Biodivers., 7, 1784 (2010), Ntalli, N., et al.: J. Agric. Food Chem., 58, 7856 (2010), Chun, M., et al.: Microchem. J., 95, 25 (2010)<br></p>

<p>Stability Moisture Sensitive<br>Applications Malonic Acid-d4 is the isotope labelled analog of Malonic Acid (M158005); a small bioactive molecule that can be used in various reactions. It is the classic example of a competitive inhibitor which acts against succinate dehydrogenase (complex II) in the respiratory electron transport chain.<br>References Weiner, N., "Malonic Acid", Org. Synth.; Coll. Vol. 2: 376<br></p>

<p>Applications Malonuric Acid is produced during degradation of sodium barbiturates.<br>References Fretwurst, F., et al.: Arzneimittel-Forschung, 8, 44-50 (1958)<br></p>

<p>Applications 11-MERCAPTOUNDECANOIC ACID (cas# 71310-21-9) is a useful research chemical.<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 3,5-Dicarboethoxy-2,6-dimethyl-1,4-dihydropyridine is a dihydropyridine derivative that have been tested for antimicrobial activities.<br>References Murthy, Y.L.. et al.: Bioorg. Med. Chem. Lett., 22, 6016 (2012); Vaitkuviene, A., et al.: Pharmacol. Rep., 58, 551 (2006);<br></p>

<p>Applications Purine (cas# 120-73-0) is a useful research chemical.<br></p>

<p>Applications 4,4-diethylcyclohexan-1-amine hydrochloride (cas# 1087747-58-7) is a useful research chemical.<br></p>

<p>Applications p-Toluoyl chloride is an aromatic compound used as a reagent to synthesize (+)-Yashabushitriol, a plant metabolite that is naturally found in the male flowers of Alnus sieboldiana matsum. p-Toluoyl chloride is also used as a reagent to prepare derivatives of Desloratadine (D290250). Desloratadine is a selective H1-receptor antagonist that has anti-inflammatory effects and is used to treat patients with allergic rhinitis.<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 Berger, W.. et al.: Ann. All. Asth. Immun., 89, 485 (2002); Fang, Z., et al.: Tetrahedron Lett., 54, 6834 (2013); Feldman, K. &amp; Simpson, R.: Tetrahedron Lett., 30, 6985 (1989); Mu, S., et al.: Chin. Chem. Lett., 24, 531 (2013)<br></p>

<p>Applications 4,4'-Di-tert-butyl-2,2'-bipyridine acts as a reagent in the preparation, antiproliferative and cytotoxic activity of apoptotic ruthenium nitrogen heterocyclic complexes via combinatorial library synthesis.<br>References Mulcahy, S. P., et al.: Dalton Trans., 39, 177 (2010)<br></p>

<p>Applications 8-Methoxycarbonyloctanoic Acid (cas# 2104-19-0) is a compound useful in organic synthesis.<br></p>

<p>Applications 3-Methoxycatechol is used to prepare polyphenolic deoxybenzoins as potential antioxidants and tyrosinase inhibitors.<br>References Ng, L., et al.: Bioorg. Med. Chem., 17, 4360 (2009)<br></p>