Ácidos y reactivos sintéticos

<p>Applications 2-Fluoroiodobenzene is used as a reagent in various organic reactions. It is used in the synthesis of spirocyclic [1,2,3]-triazolooxazine nucleosides which have antiviral properties.<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 Dell'Isola, A., et al.: Chem-Eur. J., 20, 11685 (2014)<br></p>

<p>Applications (E)-2-Thiopheneacrylic Acid is used in the synthesis of anti-HIV HEPT analogs. Also used in the synthesis of benzimidazole and caffeine (C080100) analogs as inhibitors of monoamine oxidase B.<br>References Pontikis, R. et al.: J. Med. Chem., 40, 1845 (1997); van den Berg, D. et al.: Bioorg. Med. Chem., 15, 1692 (2007);<br></p>

<p>Applications 1,4-Dichloro-2-butyne used in the synthesis of 1,4-disubstituted 1,2,3-triazoles. Also, it is used in the approach of the 20S-camptothecin family of antitumor agents.<br>References Feldman, A. et al.: Org. Lett., 6, 3897 (2004); Josien, H. et al.: Chem. Eur. J., 4, 67 (1998);<br></p>

<p>Applications (S)-(+)-3,3-Dimethyl-2-butylamine is a reagent used in organic synthesis. Used in the synthesis of allosteric modulators in the treatment of schizophrenia.<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 Wang, P. et al.: Org. Lett., 17, 3698 (2015); Turlington, M. et al.: J. Med. Chem., 56, 7976 (2013);<br></p>

<p>Applications Bis(1,5-cyclooctadiene)nickel(0) is a reagent in the synthesis of self-assembled organometallic nickel complexes as catalysts for selective dimerization of ethylene into butene.<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 Boulens, P., et al.: Organometallics, 34, 1139 (2015)<br></p>

<p>Applications N-(tert-Butoxycarbonyl)-D-prolinol is used to prepare (azetidinyl)methoxy]pyridines and 2-(aryloxymethyl) azacyclic analogs with therapeutic potetials for the treatment of central nervous system (CNS) disorders.<br>References Abreo, M., et al.: J. Med. Chem., 39, 817 (1996); Elliott, R., et al.: Bioorg. Med. Lett., 6, 2283 (1996)<br></p>

<p>Applications Di-tert-Butyl Disulfide is a general reagent used in the synthesis of a novel neuropeptide Y (NPY) Y5 receptor antagonist Velneperit) used in the treatment of obesity.<br>References Oda, S. et al.: Org. Proc. Res. Dev., 19, 531 (2015);<br></p>

<p>Applications (R)-(+)-3-Methylcyclopentanone (cas# 6672-30-6) 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 4-Nitrobenzoyl Chloride is used inorganic syntheses such as Michael additions. Also used in the synthesis of polysubstituted furanonaphthoquinoines.<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 Zhong, J. et al.: Catal. Comm., 32, 18 (2013); Wu, Z. et al.: Org. Biomol. Chem., 11, 828 (2013);<br></p>

<p>Stability Light Sensitive<br>Applications Belinostat is a novel histone deacetylase 3 selective inhibitor, which protects the β cells from cytokine-induced apoptosis.<br>References Chou, D.H., et al.: Chem. Biol., 19, 669 (2012); Hwang, J.J., et al.: Inves. New. Drugs., 30, 1434 (2012); Dizon, D.S., et al.: Gynecol. Oncol., 125, 367 (2012);<br></p>

<p>Applications MK-886 is a potent and selective inhibitor of FLAP and Cox-1.<br>References Gillard, J., et al.: Can. J. Physiol. Pharmacol., 67, 456-464 (1989);<br></p>

<p>Applications 3-Chloro-2-fluorobenzyl Bromide (cas# 85070-47-9) is a compound useful in organic synthesis.<br></p>

<p>Applications Chiral ligand for metal mediated asymmetric catalysis.<br>References Ito, H., et al.: Nat. Chem., 2, 972 (2010), Lam, K., et al.: Eur. J. Med. Chem., 45, 5527 (2010),<br></p>

<p>Applications Budralazine a new antihypertensive agent. Budralazine is a direct-acting vasodilator.<br>References Moroi, R. et al.: Chem. Pharmac. Bull., 24, 2850 (1976); Ono, K. et al.: Xenobiotica, 9, 227 (1979); Yoshioka, M. et al.: Prog. Hypertens., 1992, 309 (1992);<br></p>

<p>Applications 1-Bromooctadecane is a reagent in the preparation of branched glycosyl phosphatidyl inositol (GPI) anchors of rat brain Thy-1.<br>References Pekari, K., et al.: J. Org. Chem., 68, 1295 (2003);<br></p>

<p>Applications 7-Methoxy-2-naphthol is used as a reactant in the preparation of 9-hydroxy benzopyrene (H829410). It is also used in the preparation of (pyridyl)naphthalenes as highly potent and selective nonsteroidal dual inhibitors of CYP17/CYP11B2 for the treatment of prostate cancer to reduce risks of cardiovascular diseases.<br>References Pinto-Bazurco Mendieta, M.A.E., et al.: J. Med. Chem. 56, 6101 (2013)<br></p>

<p>Applications Trimethylamine N-Oxide Dihydrate is as an oxygen transfer agent used to promote heterometallic cluster catalyzing coordinative hydrogenation. Trimethylamine N-Oxide Dihydrate is also used as a catalyst in the preparation of thermally stable TiO2 nanorod incorporated polymers and semiconductor/metal nanocomposites.<br>References Li, Q. et al.: Fen. Cuihua, 12, 1 (1998); Patra, N. et al. Polym. Degrad. Stab., 96, 1377 (2011); Cozzoli, P.D. et al.: J. Am. Chem. Soc., 126, 3868 (2004);<br></p>

<p>Applications Hydroxylamine-O-sulfonic Acid is used in the synthesis of quinolones for the benzodiazepine site of GABAA receptors. Also used in the inhibition of PCDD as well as PCB formation in co-combustion.<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 Nilsson, J. et al.: J. Biomed. Sci. Eng., 5, 1 (2012); Pandelova, M. et al.: J. Hazard. Mat., 149, 615 (2007);<br></p>

<p>Applications (S)-5,6-Dehydro Pregabalin is derived from rac 5,6-Dehydro Pregabalin (D230055), which is an impurity of the anti-convulsant, Pregabalin (P704800).<br>References Dousa, M, et al.: J. Pharmac. Biomed. Anal., 53, 717 (2010);<br></p>

<p>Stability Light Sensitive<br>Applications Platelet aggregation inhibitor; stable analog of Prostacyclin. Antithrombotic; vasodilator (peripheral).<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 Kajikawa, N., et al.: Arzneim.-Forsch., 39, 495 (1989), Demolis, J.-L., et al.: J. Cardiovasc. Pharmacol., 22, 711 (1993), Okuda, Y., et al.: Prostaglandins, 52, 375 (1996),<br></p>

<p>Applications (S)-2-AMINO-1,1-DIPHENYL-1-PROPANOL (cas# 78603-91-5) is a useful research chemical.<br></p>

<p>Applications A specific serotonin-S2 antagonist. A selective drug for the control of behavioral disorders in epileptic and alcoholic patients.<br>References Gelders, Y.G., et al.: Acta Psychiatrica Belgica, 84, 151 (1984), Kennis, L.E.J., et al.: Drug Develop. Res., 8, 133 (1986),<br></p>

<p>Applications (Chloromethyl)cyclopropane is a used as a reagent to synthesize 6-alkylamino-9-alkylpurines, compounds that have potential to be antipsychotic agents. (Chloromethyl)cyclopropane is also used as a reagent to prepare acylmorphinans, a class of compounds that have analgesic effects in rats.<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 Kelley, J., et al.: J. Med. Chem., 40, 3207 (1997); Mohacsi, E., et al.: J. Med. Chem., 28, 1177 (1985)<br></p>

<p>Applications A useful synthetic intermediate for carbohydrate synthesis.<br></p>

<p>Applications ID 8 is an indole derivative that sustains embryonic stem cell self-renewal in long-term culture.<br>References Miyabayashi, T., et. al.: Biosci. Biotech Bioch., 72, 1242 (2008)<br></p>

<p>Stability Hygroscopic<br>Applications Ytterbium(III) Trifluoromethanesulfonate functions as a catalyst in the organic synthesis of heterocycles. Also functions as a Lewis acid in variety of organic reactions.<br>References Sakhuja, R., et al.: Synthesis, 48, 4305 92016); Molander, G. A., et al.: e-EROS Encyclopedia of Reagents for Organic Synthesis, 1 (2004)<br></p>

<p>Applications 1-Iodo-3-nitrobenzene is a reactant used int he synthesis of Vismodegib (V674700), an, antineoplastic drug that targets the Hedgehog (Hh) pathway. Inhibition of the Hh signaling may be effective in the treatment and prevention of many types of human cancers.<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 Cao, M., et. al.: Chem. Papers, 68, 1408 (2014); Gupta, S. et al.: Ther. Advances in Med. Oncology 2,237(2010)<br></p>

<p>Applications Used in the preparation of 5,7-disubstituted-4-aminopyrido[2,3-d]pyrimidines as adenosine kinase inhibitors.<br>References Dave, C., et al.: Indian J. Pharma. Sci., 48, 75 (1986),<br></p>

<p>Stability Moisture Sensitive<br>Applications An inhibitor with antitumor activity.<br>References Plumb, J., et al.: Mol. Cancer Ther., 2, 721 (2003), de Ruijter, A., et al.: Biochem. J., 370, 737 (2003), Dey, P., et al.: Curr. Med. Chem., 13, 2909 (2006), Maiso, P., et al.: Cancer Res., 66, 5781 (2006), Paris, M., et al.: J. Med. Chem., 51, 1505 (2008),<br></p>

<p>Applications Used for the preparation of N-sulfonylamino acid derivatives as metalloproteinase inhibitors.<br>References Reed, R., et al.: Biochem. J., 191, 867 (1980), Fehske, K., et al.: Biochem. Pharm., 30, 687 (1981),<br></p>

<p>Applications α-L-Idopyranose pentaacetate is used in the synthesis of mucopolysaccharides as antagonists agents.<br>References Hopwood., et al.: Clinica Chem. Acta, 123, 241 (1982), Ogamo., et al.: Carbohydr. Res., 105 (1982),<br></p>

<p>Applications 4-(Methylthio)benzaldehyde, is a building block for the synthesis of various pharmaceutical and biologically active compounds. It can be used for the synthesis of sulfur-containing terpyridine ligands. It is the intermediate for the synthesis of a class of pyrrole derivatives showing analgesic/anti-inflammatory activity.<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 Romashkina, R. B., et al.: Russian Chemical Bulletin, 61, 2265 (2012); Battilocchio, C., et al.: Bioorg. Med. Chem., 21, 3695 (2013);<br></p>

<p>Applications Reducing reagent.<br></p>

<p>Applications 2',4',6'-Trihydroxyacetophenone monohydrate (cas# 249278-28-2) is a useful research chemical.<br></p>

<p>Applications 1,5-Dichloroanthraquinone is a reagent in the preparation of anthraquinones, which has antitumor activities.<br>References Barasch, D., et al.: Eur. J. Med. Chem., 34, 597 (1999)<br></p>

<p>Applications Troxipide is a drug used in the treatment of gastroesophageal reflux disease. It is capable of inhibiting the chemotactic migration and superoxide generation in the gastric mucosa.<br>References Yu, S., et al.: Eur. J. Clin. Pharmacol., 76, 547-555 (2020)<br></p>

<p>Stability Moisture Sensitive<br>Applications 2-Acetamido-5-nitrophenylboronic acid, pinacol ester<br></p>

<p>Applications AMG 337 is a potent and selective inhibitor of mesencymal epethelial transition factor (MET factor) which has been implicated in several cancers.<br>References Boezio, A. et al.: J. Med. Chem., 59, 2326 (2016);<br></p>

<p>Applications 4-Fluoro-α-methylstyrene is used in the synthesis of Paroxetine (P205750), which is a selective serotonin reuptake inhibitor. Used as an antidepressant.<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 Lassen, J.B.: Eur. J. Pharmacol., 47, 351 (1978), Lund, J., et al.: Acta Pharmacol. Toxicol., 51, 351, (1982),<br></p>

<p>Applications SP 2509 reduces the effect of the LSD1 binding to CoREST, resulting in increased methylation of H3K4 and driving increased expression of p21, p27 and CCAAT/enhancer binding protein α in acute myeloid leukemia cells. Anti-leukemia agent.<br>References Sorna, V. et al.: J. Med. Chem., 56, 9496 (2013); Fiskus, W. et al.: Leukemia, 11, 2155 (2014);<br></p>

<p>Applications N-Acetyl-DL-Valine is an amino acid.<br>References Hirschmann R., et al.: Science, 265, 234 (1994); Gu Z. T., et al.: J. Magn. Reson., 140, 340 (1999); Bodalo, A., et al.: Enzyme Microb. Technol., 24, 381 (1999)<br></p>

<p>Applications (4R,5R)-2,2-Dimethyl-α,α,α',α'-tetra-2-naphthalenyl-1,3-dioxolane-4,5-dimethanol, is a privileged ligand analogue of TADDOLs. It can be broadly used in asymmetric synthesis. It is also shown that the titanium TADDOLate catalysts have broad application towards carbonyl addition and cycloaddition.<br>References Seebach, D., et al.: Ange. Chem. Inter. Ed., 40, 92, (20010;<br></p>

<p>Applications Tetramethoxymethane has application within an electrolyte solution for the use of rechargeable lithium batteries. It has also been used as a reactant in the synthesis of novel anti-HIV-1 compounds.<br>References Cadger, T.G. et al.: Proc. Electrochem. Soc., 88, 699 (1988); Kazmierski, W.M. et al.: J. Med. Chem., 54, 3756 (2011);<br></p>

<p>Applications: Trimethoxy(2-phenylethyl)silane is used in the loading and releasing of two anti-cancer drugs, 9-Aminoacridine (9AA) and Camptothecin (CPT) from magnetic mesoporous silica nanoparticle materials.<br>References Knezevic, N. Z., et al.: ChemPlusChem, 77, 48-55 (2012)<br></p>

<p>Applications Diethyl Bromomalonate is a chemical constituent of the asymmetric cyclopropanation of chalcones. Also used in the preparation of nanaplatforms for NIR imaging-guided photodynamic therapy of cancer cells.<br>References Herchl, R. et al.: Tetra. Lett., 54, 2472 (2013); Liu, X. et al.: Chem. Comm., 49, 3224 (2013);<br></p>

<p>Applications Zinc Acetate is used in biological studies and pharmacological activity of motexafin gadolinium disruptions of zinc metabolism in human cancer cell lines.<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 Magda, D., et al.: Cancer Res., 65, 3837 (2005);<br></p>

<p>Applications 4-Nitro-benzeneethanol is a useful synthetic intermediate. It can be used to synthesize N-phenylethylindole carboxamides as SAR study of allosteric modulators of CB1 receptor. It can also be used to prepare 2-aza-2'-deoxyinosine-containing oligodeoxyribonucleotide duplexes.<br>References Piscitelli, F., et al.: J. Med. Chem., 55, 5627 (2012); Acedo, M., et al.: J. Org. Chem., 60, 6262 (1995)<br></p>

<p>Applications Silver Tetrafluoroborate is an active reagent in the preparation of metal-organic synthetic transporters which are efficient chlorides and antibiotic transmembrane transporters. A deprototecting reagent. Reagent in the preparation and antimicrobial activity of water-soluble silver (I) complexes of metronidazole drug.<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 Kempf, J., et al.; Chem. Eur. J., 23, , 6441 (2017); Yoshida M., et al.: Chem. pharm. bull., 38, 273 (1990); Kalinowska-Lis, U., et al.: Dalton Transactions, 44, 8178 (2015); Liu, P., et al.: Org. Lett., 19, 3482 (2017); Varela, I., et al.: ACS Catal., 7, 2397 (2017)<br></p>

<p>Stability Hygroscopic<br>Applications Omeprazole Sodium Salt is the salt analogue of Omeprazole (O635000), which binds covalently to proton pump. It inhibits gastric secretion. Used as an anttiulcerative.<br>References Muller, P., et al.: Arzneimittel-Forsch., 33, 1685 (1983); Wallmark, B., et al.: Biochim. Biophys. Acta., 778, 549 (1984); Morii, M., et al.: J. Biol. chem., 268, 21553 (1993); Ritter, M., et al.: Br. J. Pharmacol., 124, 627 (1998)<br></p>

<p>Applications An Aurora kinase inhibitor, used to treat patients with chromic myeloid leukemia. It is a COVID19-related research product.<br>References Fancelli, D., et al.: J. Med. Chem., 49, 7247 (2006), Carpinelli, P., et al.: Mol. Canc. Ther., 6, 3158 (2007), Coumar, M., et al.: J. Med. Chem., 52, 1050 (2009),<br></p>

<p>Stability Moisture Sensitive<br>Applications Zinc Di[bis(trifluoromethylsulfonyl)imide] is a reactant used in the assembly of pyrene-based Schiff base MII4L6 architectures.<br>References Ronson, T. et al.: J. Am. Chem. Soc., 137, 14502 (2015); Riddell, I. et al.: Chem. Sci., 6, 3533 (2015);<br></p>

<p>Applications Protected Glycidol, used as an intermediate in the preparation of neurochemicals.<br>References Wang, J., et al.: J. Med. Chem., 48, 6271 (2005), Qian, L., et al.: ChemMedChem, 1, 376 (2006), Li, Y., et al.: Bioorg. Med. Chem. Lett., 19, 5037 (2009),<br></p>