Building Blocks

<p>Applications 3-Hydroxy Ketoprofen is related to rac Ketoprofen (K200800) a Anti-inflammatory drug. 3-Hydroxy Ketoprofen is used to study the metabolism of ketoprofen<br>References Liversidge, G.G., Anal. Profiles Drug Subs., 10, 443 (1981), Jamali, F., et al.: Clin. Pharmacokinet., 19, 197 (1990), Huq, F., et al.: Pure Appl. Chem., 2, 229-234 (2007)<br></p>

<p>Applications ethyl 2-cyclopropyl-2-hydroxyacetate (cas# 1185387-66-9) is a useful research chemical.<br></p>

<p>Applications trans-Campestanyl Ferulate is used for synthesis of trans-feruloyl-β-sitostanol.<br>References Condo, A., et al.: J. Agric. Food Chem., 49, 4961 (2001);<br></p>

<p>Applications An intermediate in the production of many biological inhibitors.<br>References Lambertucci, C., et al.: Bioorg. Med. Chem., 17, 2812 (2009), Lebsack, A., et al.: Bioorg. Med. Chem. Lett., 19, 40 (2009), Griffith, D., et al.: J. Med. Chem., 52, 234 (2009),<br></p>

<p>Applications Acetone oxime was one of the reagents used as a part of preparation of arylbenzoxazoles as potent and selective estrogen receptor-β ligands.<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 Malamas, M., et al.: J. Med. Chem., 47, 5021 (2004)<br></p>

<p>Applications N-Methylsuccinimide is used as a model compound to investigate the mechanism of enolization step by density-functional theory (DFT) calculations. N-Methylsuccinimide is a metabolite of N-methyl-2-pyrrolidone (NMP) and its presence in plasma and urine can be used as a biomarker of exposure to NMP<br>References Takahashi, O., et al.: Chem. Biodivers., 7, 1349 (2010)<br></p>

<p>Applications Carboxymethoxyamine Hemihydrochloride (cas# 2921-14-4) is a compound useful in organic synthesis.<br></p>

<p>(1-Bromo-2,2-difluoroethyl)benzene is a chemical compound that is used as a reaction component in the synthesis of other compounds. It can be used to synthesize high-quality research chemicals and speciality chemicals. It is also a versatile building block for the synthesis of complex compounds. This product has been assigned CAS No. 74492-20-9 and is considered a fine chemical.</p>

<p>3,4-Dihydroxybenzaldehyde is an active compound that is a protocatechuic aldehyde. It has been shown to inhibit protein oxidation and kidney injury. 3,4-Dihydroxybenzaldehyde also inhibits the production of bcl-2 protein and growth factor-β in rat urine. This compound has been used in Chinese medicinal preparations as well as in control methods for oxidizing agents.</p>

<p>2,6-Dichloro-3-deazapurine is an isomer of the nucleoside guanosine. It has been shown to inhibit the synthesis of viruses in cell cultures and may be useful in the treatment of leukemia. The synthesis of 2,6-dichloro-3-deazapurine can be achieved through a solid-phase synthesis that uses synthons as starting materials. The molecular modelling studies have shown that this molecule has a potential to bind to adenosine receptor subtypes A2a, A2b, and A3.</p>

<p>Intermediate in the synthesis of tofacitinib</p>

<p>Cationic surfactant; antiseptic</p>

<p>2,5-Dibromopyrazine is a heterocyclic compound that can be synthesized by the Suzuki coupling reaction of 2-bromo-1,3-dibromopropane with an acceptor. It has been shown to have glycemic parameters and a high rate enhancement for the water molecule photophysical isomerization reaction. Structural isomers of 2,5-dibromopyrazine exist as well and are thought to have different rates of photocatalytic activity. The rate enhancement may be due to the increase in electron density on the heteroatoms in the ring.</p>

<p>L-Histidine methyl ester dihydrochloride is a β-amino acid with the chemical formula HNCH2CH(CH3)CO2H. It has the functional group of an isopropyl group and a chloride ion. L-Histidine methyl ester dihydrochloride has been shown to bind to receptors in the central nervous system that are involved in pain perception. As a result, it can be used for the treatment of neuropathic pain, chronic pain, and cancer pain. This drug also inhibits nitric oxide production by binding to iron ions or copper ions. L-Histidine methyl ester dihydrochloride has been shown to have antiinflammatory effects as well as antioxidant properties.</p>

<p>2,6-Dichloropyridine is an organohalide used as a reagent for asymmetric catalysis. It is use as a precursor for the synthesis of antibacterial agents, for example the synthesis of the antibiotic enoxacin.</p>

<p>4-Hydroxyquinoline is a chemical compound that has been shown to have anticancer, anti-inflammatory, and antiviral properties. It is an inhibitor of the enzyme tyrosinase, which is required for the production of melanin. 4-Hydroxyquinoline has also been shown to suppress bowel inflammation by inhibiting the synthesis of 3-hydroxyanthranilic acid in cells. 4-Hydroxyquinoline has been found to be effective against Herpes Simplex Virus Type 1 (HSV1) in cell culture and in vitro assays. <br>4-Hydroxyquinoline's photochemical properties make it a useful precursor for the synthesis of other biologically active compounds. This chemical undergoes a reaction with trifluoroacetic acid to form diazonium salt intermediate, which then reacts with hydrogen peroxide to form an active oxygen species that damages DNA and kills cells.</p>

<p>2,4-Dimethyl-3-nitropyridine is a heterocyclic organic compound. It is an important and versatile building block for the synthesis of complex compounds. 2,4-Dimethyl-3-nitropyridine can be used as a reagent in organic synthesis and other chemical reactions. In addition to its use as a reactant, this compound has been employed as a useful scaffold for the preparation of other heterocycles and fine chemicals. The CAS number for 2,4-dimethyl-3-nitropyridine is 1074-76-6.</p>

<p>2-(3-Hydroxypropyl)benzimidazole is a chloroform extract of the bark of the tree, Pongamia pinnata. It has been shown to have antibacterial and antitumor activity. 2-(3-Hydroxypropyl)benzimidazole has been found to be active against methicillin-resistant Staphylococcus aureus (MRSA), showing strong inhibitory effects on bacterial cell growth in vitro. The mechanism of action may be due to its ability to bind to DNA and RNA, preventing transcription and replication. 2-(3-Hydroxypropyl)benzimidazole also inhibits protein synthesis by binding to ribosomes and interfering with the function of enzymes that are involved in this process such as cytochrome c reductase, glutathione reductase, and 3-ketoacyl coenzyme A thiolase.</p>