Reagenti sintetici

<p>Applications 2,4-Dichloro-5-trifluoromethylpyrimidine is a reactant in the preparation of pyrimidine derivatives as inhibitors of gene ALK protein Kinase phosphorylating kinase and as cell proliferation inhibitors.<br>References Yang, E.H., et. al.: Bull. Korean Chem. Soc., 34, 3129 (2013)<br></p>

<p>Applications An optically active resolving agent.<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 Helv. Chim. Acta, 61, 2773 (1978)<br></p>

<p>Applications Methyl 11-bromoundecanoate is a brominated fatty acid building block, used in the synthesis of Emmyguyacins A and B, which are proposed inhibitors of the influenza virus.<br>References Jana, S.; et al.: Org. Lett., 20, 6938 (2018).<br></p>

<p>Applications Antineoplastic adjunct (chemosensitizer).<br>References Boesch, D., et al.: exp. Cell Res., 196, 26 (1991), Lush, R.M., et al.: J. Clin. Pharmacol., 37, 123 (1997), Scott, M.G., et al.: Clin. Chem., 43, 505 (1997), Advani, R., et al.: Blood, 93, 787 (1999),<br></p>

<p>Applications 3'-Bromo-4'-methylacetophenone is used as a starting material in the synthesis of mansonone E which is used to make mansonone E dervivatives. These derivatives are potent inhibitors of topoisomerase II (Topo II) and topoisomerase I (Topo I) and are also potent antitumor agents. 3'-Bromo-4'-methylacetophenone is also used as a reagent in the synthesis of BAF312, Siponimod which has been tested in the treatment of patients suffering from relapsing-remitting multiple sclerosis.<br>References Fang, X., et al.: J. Chem. Res., 38, 137 (2014); Huang, Z., et al.: Eur. J. Med. Chem., 68, 58 (2013); Pan, S., et al.: ACS Med. Chem. Lett., 4, 333 (2013)<br></p>

<p>Stability Unstable in solution. Small amounts of precipitate should have no effect on use.<br>Applications 1-Chloro-N,N-2-trimethylpropenylamine acts as a reagent in the synthesis and antitumor activity of (-)-bassianolide in human cancer cells through cell cycle arrest. Enantioselective total synthesis of nannocystins A and A0 as elongation factor 1 inhibitors. Total synthesis of (-)-caprazamycin A with antibacterial activity against Mycobacterium tuberculosis (TB) via diastereoselective aldol reaction.<br>References Mun, B., et al.: Bioorg. Chem., 69, 64 (2016); Huang, J., et al.: Org. Lett., 18, 4702 (2016); Nakamura, H., et al.: Angew. Chem., Int. Ed., 54, 3136 (2015)<br></p>

<p>Applications α,α,α-Trifluorotoluene, is used as a specialty solvent in organic synthesis and an intermediate in the production of pesticides and pharmaceuticals.<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 Skelly, P. D., et al.: Handbook for Critical Cleaning, 1, 191 (2011);<br></p>

<p>Applications (S)​-​(+)​-​Pantolactone is a versatile cyclic ester reactant used in the preparation of tunable ligands carbohydrate-derived diarylphosphinites for asymetric catalysis hydrovinylation of styrene derivatives.<br>References Park, H., RajanBabu, T.: J. Am. Chem. Soc., 124, 734 (2002);<br></p>

<p>Applications (R)-α-Phenethyl Alcohol, is a chiral building block used for the synthesis of various pharmaceutical compounds. It can be used for the preparation of biologically active cyclitols.<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 Redgrave, A. J., et al.: No pp., Dissertation (1991);<br></p>

<p>Applications Chlorotripyrrolidinophosphonium Hexafluorophosphate acts as a peptide coupling reagent or condensing agent for phosphinate ester formation.<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 Prasad, K. et al.: Int. J. Pharm. Sci. Rev. Res., 8, 108 (2011); Winqvist, A. et al.: Eur. J. Org. Chem. 10, 1705 (2008);<br></p>

<p>Stability Moisture Sensitive<br>Applications N,N-Dimethylphosphoramidodichloridate functions as a reagent used in the inhibition of acetylcholinestrase and butyryl cholinestrase by nerve agent surrogates. Also, the are used as reagents in the synthesis and in the antitumor activity of nonsymmetric phosphoric acid triamides.<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 Meek, E. C., et al.: Toxicol. Sci., 126, 525 (2012); Kosykhova, L., et al.: Pharm. Chem., 34, 525 (2000)<br></p>

<p>Applications Inhibitor of phosphatidylinositol 3-kinases, P13K and mTOR. Potent PI3K/mTOR Dual Inhibitor.<br>References Konstantinidou, G., et al.: Cancer Res., 69, 7644 (2009), Frederick, R., et al.: Bioorg. Med. Chem. Lett., 19, 5842 (2009), Pollizzi, K., et al.: Mol. Cancer, 8 (2009),<br></p>

<p>Applications Rhenium Carbonyl, is used as a catalyst and in material science. iIt is also a key starting material used for the synthesis of other rhenium carbonyl complexes. It plays an important role in metathesis, reforming and hydrogenation reactions.<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 Kremlev, K. V., et al.: J. Surf. Ingestig.-X-Ray Synchro. 2015, 9 (4), 694-698.; Di, X., et al.: Catal. Sci. Technol. 2015, 5 (4), 2441-2448.;<br></p>

<p>Applications Triphenylsilylamine is used as a reagent to produce 2-Amino-3-hydroxy-indoles with potent in vivo antimalarial activity. Triphenylsilylamine is also used to modify Mo/HZSM-5 catalysts and is predicted to have effects on selectivity in the methane-to-benzene (MTB) reaction.<br>References Kikuchi, S., et al.: J. Catal., 242, 349 (2006); Urgaonkar, S., et al.: Org. Lett., 12, 3998 (2010);<br></p>

<p>Applications BL 918 is a potent small-molecule activator of UNC-51-like kinase 1 (ULK1), a serine-threonine kinase involved in autophagy. Promotes cytoprotective autophagy in MPP+-treated SH-SY5Y cells, via the ULK complex. Improves motor dysfunction and reduces loss of dopaminergic neurons, mediated by MPTP, in in vivo models of Parkinson’s disease.<br>References Ouyang, Liang., et al.: J. Med. Chem., 61, 2776 (2018),<br></p>

<p>Applications N-Methoxy-N-methylbenzamide is used to prepare orally bioavailable tetrasubstituted imidazoles as inhibitors of p38 mitogen-activated protein kinase. It is used to synthesize benzofuran and benzothiophene biphenyls as inhibitors of protein tyrosine phosphatase 1B with antihyperglycemic properties.<br>References Liverton, N., et al.: J. Med. Chem., 42, 2180 (1999); Malamas, M., et al.: J. Med. Chem., 43, 1293 (2000)<br></p>

<p>Applications 3-Fluoro-4-methoxybenzaldehyde is a useful reagent in the synthesis of resveratrol derivatives as potent inhibitors of lysine specific demethylase 1 (LSD1), a therapeutic target for cancer treatment and other related diseases. Also a reagent for the synthesis of substituted pyrazolyl piperidine derivatives as antiplatelet agents with antiplatelet aggregation activity in the human body.<br>References Duan, Y., et al.: Eur. J. Med. Chem., 126, 246 (2017); Soni, J. Y., et al.: J. Heterocyclic Chem., 54, 1279 (2017)<br></p>

<p>Applications Iron(II) Chloride is used in preparation of a variety of organically templated iron phosphates. It also serves as a reducing flocculating agent in wastewater treatment. It is the precursor to hydrated iron(III) oxides that are magnetic pigments.<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 Lii, K., et al.: Chem. Mater., 10, 2599 (1998); Wildermuth, E., et al.: Ullmann’s Encyclopedia of Industrial Chemistry Wiley-VCH, Wienheim (2005)<br></p>

<p>Applications Trimethylboroxin (50% Solution in THF) is used in a diverse array of areas, including as a polymerization additive. Trimethylboroxin is also used in the preparation of CBS catalysts for asymmetric reductions.<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 Gilmore, N., et al.: Tetrahedron Asy., 14, 2115 (2003); Najera, C., et al.: Adv. Synth. Catal., 346, 1798 (2004);<br></p>

<p>Applications N-DesBoc Docetaxel is an impurity in the synthesis of Docetaxel (D494420), a semisynthetic derivative of Paclitaxel. An antimitotic agent that promotes the assembly of micro-tubules and inhibits their de-polymerization to free tubulin. An antine oplastic.<br>References Ringel, I., et al.: J. Natl. Cancer Inst., 83, 288 (1991), Extra, J.-M., et al.: Cancer Res., 53, 1037 (1993)<br></p>

<p>Applications A tyrosine kinase inhibitor; it is used to prepare formulation for treating primary or secondary cancer.<br>References Veronese, M., et al.: Br. J. Cancer, 92, 1846 (2005), Hofheinz, R., et al.: Onkologie, 29, 563 (2006), Meyerhardt, J., et al.: J. Clin. Oncol., 24, 1892 (2006), Hanauske, A., et al.: Clin. Cancer Res., 13, 523 (2007),<br></p>

<p>Applications Tri-tert-butyl 1,4,7,10-Tetraazacyclododecane-1,4,7-triacetate with amide ligands bearing positively charged terbium complexes are used for sensitive detection of NADPH-dependent enzyme activities.<br>References Ito, H., et al.: Chem. Commun., 51, 8319-8322 (2015)<br></p>

<p>Applications Indium element is used in the synthesis of therapeutic particles containing metal ions; characterized by the use of unique ligand sets capable of making the metal ion complex soluble in biolgical media to induce selective toxicity in diseased cells.<br>References Dagher, Z., et al.: Toxicology, 225, 12 (2006), Yoshida, T., et al.: Biol. Pharm. Bull., 33, 780 (2010), Danielsen, P., et al.: Chem. Res. Toxico.,l 2011, 24, 168 (2011),<br></p>

<p>Applications An intermediate in the preparation of pentafluoropentane-1-thiol: an important chain of anti-breast cancer agents.<br>References By Li, X. et al.: Tetrahedron Lett., 35, 9141 (1994);<br></p>

<p>Applications A reagent used in the synthesis of Pitavastatin.<br>References Mukaiyama, H., et al.: Chem. Pharm. Bull., 55, 881 (2007), Paruch, K., et al.: Bioorg. Med. Chem. Lett., 17, 6220 (2007),<br></p>

<p>Applications 5-Bromopentyltrimethylammonium Bromide (cas# 15008-33-0) is a compound useful in organic synthesis.<br></p>

<p>Applications Copper (I) bromide is used as a reagent to brominate electron-rich aromatic compounds (e.g. Phenol: P318000). Copper (I) bromide is also used to brominate aliphatic ketones (e.g. Acetone: A163800).<br>References Bhatt, S. &amp; Nayak, S.: Synth. Comm., 37, 1381 (2007); Kojima, Y. &amp; Kawaguchi, S.: Bull. Chem. Soc. Jpn., 45, 1293 (1972)<br></p>

<p>Applications 1,1-(Ethylenedioxy)-3-bromopropane is used in the synthesis of EGFR inhibitors. Also used in the synthesis of orally active agents of cancer and cell proliferation with quinoline substructures.<br>References Zhang, X. et al.: Arch. Pharm., 346, 44 (2013); Lee, Y. et al.: J. Med. Chem., 55, 10363 (2012);<br></p>

<p>Applications: An orally active, synthetic nonpeptide renin inhibitor. Antihypertensive.<br>References Lefevre, G., et al.: J. Immunoassay, 21, 65 (2000), Allikments, K., et al.: Curr. Opin. Invest. Drugs, 3, 1479 (2002), Wood, J.M., et al.: Biochem. Biophys. Res. Commun., 308, 698 (2003), Grandman, A.H., et al.: Circulation, 111, 1012 (2005),<br></p>

<p>Applications Dihydrotetrakis(triphenylphosphine)ruthenium is used in preparation of Acyl Pyrrole derivatives catalyzed by transition metal Ruthenium.<br>References Wu, Y., et al.: Faming Zhuanli Shenqing, (2019);<br></p>

<p>Applications Benzyltributylammonium Chloride (cas# 23616-79-7) is a useful research chemical.<br></p>

<p>Applications 3-Chloro-2-hydroxypropyltrimethyl ammonium chloride is used in the preparation of multifunctional cationized cotton fabric based on TiO2 nanomaterials.<br>References Farouk, A., et la.: Int. J. Biol. Macromolecules, 61, 230 (2013);<br></p>

<p>Applications Bismuth(III) Trifluoromethanesulfonate (3:1) is a catalyst used in Friedel-Crafts acylation and cycloisomerization of allene-enol ethers.<br>References Repichet, S., et. al.: Eur. J. Org. Chem., 12, 2743 (1998); Ondet, P., et. al.: Org. Lett., 17, 1002 (2015)<br></p>

<p>Applications (Z)-2-((Furan-2-ylmethyl)sulfinyl)-n-(4-((3-(piperidin-1-ylmethyl)pyridin-2-yl)oxy)but-2-en-1-yl)acetamide is a Histaminic H2 receptor antagonists in ulcer disease. Also, it is a model compound used to investigate the binding mechanism between antiulcer drugs and human serum albumin (HSA).<br>References Patel, P. B., et al.: World J. Pharm. Sci., 5, 532-540 (2016); Yang, h., et al.: Arch. Biochem. Biophys., 606, 81-89 (2016);<br></p>

<p>Applications 2-Adamantanamine Hydrochloride (cas# 10523-68-9) is a useful research chemical.<br></p>

<p>Applications A potent and selective inhibitor of NAE. An inhibitor of NEDD8-activating enzyme as a new approach to treat cancer. The ubiquitin-proteasome pathway mediates the destruction of unwanted proteins. Potent NAE inhibitor; NEDD8 E1 Activating Enzyme Inhibitor.<br>References Haas, A., et al.: J. Biol. Chem., 257, 10329 (1982), Walden, H., et al.: Nature, 422, 330 (2003), Kane, R., et al.: Clin. Cancer Res., 13, 5291 (2007), Saha, A., et al.: Mol. Cell., 32, 21 (2008),<br></p>

<p>Applications 1,2-Benzisoxazole has therapeutic uses. It could be useful for treating parkinsonism.<br>References Panza, F., et al.: Expert Opin. Pharmacother., (2020)<br></p>

<p>Applications 2,3-Diaminopyridine is used as a reagent in the synthesis of novel imidazopyridine derivatives which can exhibit cytotoxic activity against MCF-7 human breast adenocarcinoma cell line. 2,3-Diaminopyridine is also used in the preparation of non-camptothecin topoisomerase I inhibitors which exhibit antitumor activity.<br>References Puskullu, M.O., et al.: Chem. Heterocyc. Compd., 51, 723 (2015); Zhang, C., et al.: Bioorg. Med. Chem. Lett., 25, 4693 (2015)<br></p>

<p>Applications N-(4-Methoxybenzyl)-N-methylamine is used in the synthetic preparation of many types of compounds, including the synthesis of trifluoromethyl-sulfonimidamides from sulfinamides as well as the preparation of piperazinylquinazoline amine compounds as toll-like receptor 9 signaling antagonists for treatment of immune disorders.<br>References Richards-Taylor, C.S.; et al.: J. Org. Chem, 82, 9898 (2017); Talukdar, A.; et al.: PCT Int. Appl. 89pp. Patent 2017 CODEN:PIXXD2<br></p>

<p>Applications Potent inhibitor of heat shock protein 90 (Hsp90). 17-AAG is a less toxic analog than Geldanamycin. It induces apoptosis and displays antitumor effects. 17-AAG inhibits the activity of oncogenic proteins such as N-ras, Ki-ras, c-Akt, and p185erB2.<br>References Schnur, R.C., et al.: J. Med. Chem., 38, 3806 (1995), Nimmanapalli, R., et al.: Cancer Res., 61, 1799 (2001), Basso, A.D., et al.: Oncogene, 21, 1159 (2002),<br></p>

<p>Applications (S)-(-)-2-Methylbutanol is a reagent in the isolation of KM-01 from the two fungi Drechslera avenae and Pycnoporus coccineus<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 Kim, S., et al.: Bioorg. Med. Chem., 6, 1975 (1998);<br></p>

<p>Applications Labelled Acetic Acid is used for analysis and profiling of biological samples resolved through NMR spectroscopy. It helps with the labelling of RNA for high resolution NMR.<br>References Cahoreau, E. et al.: Anal. Bio., 427, 158 (2012);<br></p>

<p>Applications GBR-12909 is a potent dopamine transport blocker studied extensively in rats; it has also been classified as being able to release norepinephrine more potently than it releaes dopamine and seratonin in biological studies.<br>References Rothman, R.B.; et al.: Synapse, 39, 32 (2001)<br></p>

<p>Applications Lanthanum(III) Trifluoromethanesulfonate is a catalyst that is used for the trans-esterification of Jatropha curcas L. oil with methanol and higher alcohols. Studies on rats and mice showed that Lanthanum(III) Trifluoromethanesulfonate is a moderately hazardous substance causing slight irritation of the skin and that the maximum permitted concentration in the workplace is 2.0 mg/m3.<br>References Daniel, L., et al.: J. Am. Oil Chem. Soc., 91, 325 (2014); Zhurba, O.M., et al.: Toksikologicheskii Vestnik, no vol., 20 (2005)<br></p>

<p>Applications (3R,5R)-Atorvastatin Sodium Salt is an Atorvastatin impurity in bulk drug and tablets.<br>References Posvar, E., et al.: J. Clin. Pharmacol., 36, 728 (1996), Lea, A., et al.: Drugs, 53, 828 (1997), Miao, X., et al.: J. Chromatogr., 998, 133 (2003),<br></p>

<p>Applications 4-(4-Boc-piperazine-1-carbonyl)phenylboronic acid pinacol ester<br></p>

<p>Impurity Atomoxetine EP Impurity D<br>Applications m-Methyl Atomoxetine Hydrochloride (Atomoxetine EP Impurity D) is an impurity of Atomoxetine (A791400), a norepinephrine reuptake inhibitor.<br>References Farid, N.A., et al.: J. Clin. Pharmacol., 25, 296 (1985), Gehlert, D.R., et al.: J. Neurochem., 64, 2792 (1995), Hwamg. et al.: Neurosci. Lett., 265, 151 (1999), Ring, B.J., et al.: Drug Metab. Dispos., 30, 319 (2002),<br></p>

<p>Applications 2-Methoxybenzoyl Chloride is an aromatic acyl chloride derived from anisic acid. 2-Methoxybenzoyl Chloride is used in the preparation of a wide range of compounds such as anti-virals, anti-bacterials and antitumor agents.<br>References Li, Z. et al.: Chem. Biol. Drug Des., 79, 1018 (2012); Liu, W. et al.: Huax. Tong., 74, 665 (2011); Sousa, E. et al.: Eur. J. Med. Chem., 44, 3830 (2009);<br></p>

<p>Applications 1-Bromo-3,5-difluorobenzene is used in the synthesis of selective antagonists of GluN2C/GluN2D is used in the synthesis of COX-2 inhibitors as anti-inflammatory agents and anti-cancer agents.<br>References Khanna, I. et al.: J. Med. Chem., 40, 1634 (1997); Pommery, N. et al.: J. Med. Chem., 47, 6195 (2004);<br></p>

<p>Applications Silver Carbonate is used in organic synthesis in the Koenigs-knorr glycosylation reaction. It is also known as Fetizon's reagent acting as an oxidising agent on celite forming lactones form diols.<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 Fetizon, M., et al.: J. Chem. Soc. Chem. Comm., 19, 1118 (1969);<br></p>

<p>Applications 4-(Bromomethyl)benzoic Acid Methyl Ester is an ester derivative of a bromoalkylated benzoic acid. 4-(Bromomethyl)benzoic Acid Methyl Ester is used in the preparation of potential anti-HIV agents. It is also used as a catalyst for rearrangement of benzylthiothiazoline derivatives in the preparation aldose reductase inhibitors.<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 Cushman, M. et al.: Bioorg. Med. Chem. Lett., 8, 833 (1998); Nagao, Y. et al.: Chem. Pharmac. Bull., 36, 509 (1988);<br></p>

<p>Applications Acetylhistamine, is a histamine metabolite, and can be used as a potential biomarker of histidine metabolism for anaphylactoid reactions.<br>References Xu Y, et al. Asian Pac J Allergy Immunol. 2017 Dec;35(4):224-232.;<br></p>

<p>Applications Sodium Metasilicate is an antibacterial pharmaceutical compound containing Sodium Hydrogen Carbonate.<br>References Karaagac, M., et al.: Turk. Pat. Appl., (2017);<br></p>

<p>Stability Hygroscopic<br>Applications Ethoxyamine Hydrochloride acts as a reagent in the preparation of biflorin derivatives (hydrazones, oximes, terpene ketones) and determination of their activity as antibacterial and anticancer agents.<br>References Souza, L. G., et al.: Bioorg. Med. Chem. Lett., 26, 435 (2016)<br></p>

<p>Applications Nimustine Hydrochloride is a DNA alkylator and cross-linking agent. It is used in chemotherapy in a part of anti-cancer cocktail used to treat malignant melanoma.<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 Matsumoto, T. et al.: J. Eur. Acad. Dermatol. Venereol., 27, 1514 (2013);<br></p>

<p>Stability Hygroscopic<br>Applications A semi-synthetic derivative of Podophyllotoxin. Antineoplastic.<br>References Stahlen, H., Eur. J. Cancer, 6, 303 (1970), Hacker, M., et al.: Cancer Res., 37, 3287 (1977), Clark, P.I., et al.: Clin. Pharmacokinet., 12, 223 (1987),<br></p>

<p>Applications R-(-)-Rolipram is a phosphodiesterase IV (PDE4) inhibitor and anti-inflammatory agent with some antidepressant activity. It is the R isomer of (±)-Rolipram (R640040). Potent PDE4 inhibitor.<br>References Semmler, J., et al.: Int. J. Immunopharmacol.: 15, 409 (1993); Sommer, N., et al.: Nat. Med.: 1, 244 (1995); Robichaud, A., et al.: J. Clin. Invest., 110, 1045 (2002); Card, G., et al.: Structure: 12, 2233 (2004);<br></p>

<p>Applications Methyl Dimethoxyacetate is used as a reagent in the synthesis of benzimidazole derivatives for use as respiratory syncytial virus inhibitors.<br>References Cooymans, Ludwig Paul; D., et al. PCT Int. Appl. WO 2012080446 A1 20120621. Jun 21, 2012<br></p>