Chiral Organic Compounds
Chiral organic compounds are molecules that possess non-superimposable mirror images, a property known as chirality, which plays a crucial role in various chemical and biological processes. These compounds are essential in the development of pharmaceuticals, agrochemicals, and fine chemicals, where the specific orientation of molecules can significantly impact their function and efficacy. At CymitQuimica, we offer a comprehensive range of high-purity chiral organic compounds, including enantiomers and diastereomers, meticulously sourced and tested to meet the stringent demands of both research and industrial applications. Our catalog includes chiral catalysts, auxiliaries, and building blocks that are pivotal in asymmetric synthesis and stereoselective reactions. By providing top-quality chiral organic compounds, we support researchers and professionals in achieving precise and efficient stereochemical outcomes, driving advancements and innovation in fields such as medicinal chemistry, biotechnology, and materials science.
Found 3783 products of "Chiral Organic Compounds"
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(R)-(+)-Timolol Maleate
CAS:Controlled Product<p>Impurity Timolol EP A; Timolol BP Impurity A; Timolol USP Related Compound A<br>Applications Antihypertensive; antiarrhythmic (class II); antianginal; antiglaucoma agent.Timolol EP A; Timolol BP Impurity A; Timolol USP Related Compound A<br>References Wasson, et al.: J. Med. Chem., 15, 651 (1972), Franciosa, et al.: Clin. Pharmacol. Ther., 13, 138 (1972), Heel, R.C., et al.: Drugs, 17, 38 (1979), Rofman, B.A., et al.: Hypertension, 2, 643 (1980), Mazzo, D.J., et al.: Anal. Profiles Drug Subs., 16, 641 (1987),<br></p>Formula:C13H24N4O3S·C4H4O4Color and Shape:NeatMolecular weight:432.497-Epi-10-oxo Docetaxel
CAS:Controlled Product<p>Impurity Docetaxel EP Impurity D<br>Applications 7-Epi-10-oxo Docetaxel (Docetaxel EP Impurity D) is a Docetaxel (D494420) injection impurity D.<br>References Hanna, I., et al.: Cancer Res., 60, 3440 (2000), Bournique, B., et al.: Br. J. Clin. Pharmacol., 52, 53 (2001), McFadyen, M., et al.: Biochem. Pharmacol., 62, 207 (2001), Vasu Dev, R., et al.: J. Pharm. Biomed. Anal., 40, 614 (2006),<br></p>Formula:C43H51NO14Color and Shape:White SolidMolecular weight:805.86ent-Tadalafil
CAS:Controlled Product<p>Impurity Tadalafil EP Impurity B<br>Applications Tadalafil (T004500) analog. Tadalafil Impurity (6S,12aS)<br>References Daugan, A., et al.: J. Med. Chem., 46, 4533 (2003), Jiang, W., et al.: Bioorg. Med. Chem., 12, 1505 (2004),<br></p>Formula:C22H19N3O4Color and Shape:NeatMolecular weight:389.40cis-ent-Tadalafil
CAS:Controlled Product<p>Impurity Tadalafil EP Impurity C<br>Applications The (6S)-cis-enantiomer of Tadalafil (T004500). Tadalafil Impurity (6S,12aR)<br>References Aldridge, J., et al.: Br. Med. J., 318, 669 (1999), Daugan, A., et al.: J. Med. Chem., 46, 4533 (2003), Vredenbregt, M., et al.: J. Pharm. Biomed. Anal., 40, 840 (2006),<br></p>Formula:C22H19N3O4Color and Shape:White To Off-WhiteMolecular weight:389.40cis-Tadalafil
CAS:Controlled Product<p>Impurity Tadalafil EP Impurity A<br>Applications The (6R)-cis-enantiomer of Tadalafil (T004500). Tadalafil Impurity (6R,12aS)<br>References Aldridge, J., et al.: Br. Med. J., 318, 669 (1999), Daugan, A., et al.: J. Med. Chem., 46, 4533 (2003), Vredenbregt, M., et al.: J. Pharm. Biomed. Anal., 40, 840 (2006),<br></p>Formula:C22H19N3O4Color and Shape:Off-WhiteMolecular weight:389.40Dehydro Simvastatin
CAS:Controlled Product<p>Impurity Simvastatin EP Impurity C<br>Applications Dehydro Simvastatin (Simvastatin EP Impurity C) is a Simvastatin (S485000) impurity.<br>References Carlucci, G., et al.: J. Pharm. Biomed. Anal., 10, 693 (1992), Nagarajan, R., et al.: Langmuir, 16, 6400 (2000), Wang, L., et al.: J. Pharm. Biomed. Anal., 21, 1243 (2000),<br></p>Formula:C25H36O4Color and Shape:WhiteMolecular weight:400.55Desacetyl Forskolin
CAS:Controlled Product<p>Applications Desacetyl Forskolin is an analogue of Forskolin (F701800). Desacetyl Forskolin was tested for its ability to activate rat brain adenylate cyclase, activate detergent-solubilized rat brain adenylate cyclase, increase cyclic AMP in intact S49 wild-type cells, and inhibit the binding of 3H-forskolin to rat brain membranes.<br>References Desouza, N., et al.: Med. Res. Rev., 3, 201 (1983); Seamon, K., et al.: J. Med. Chem., 26, 436 (1983); Seguin, E., et al.: Planta Medica, 54, 4 (1988);<br></p>Formula:C20H32O6Color and Shape:NeatMolecular weight:368.46N-Jasmonyl-L-Isoleucine (Mixture of Diastereomers)
CAS:Controlled Product<p>Applications N-Jasmonyl-L-Isoleucine (Mixture of Diastereomers) is a plant horomone.<br>References Chen, Y., Chen, Z.: J. Separation Sci., 36, 892 (2013)<br></p>Formula:C18H29NO4Color and Shape:NeatMolecular weight:323.43(-)-β-Bisabolene (>85%)
CAS:Controlled Product<p>Applications Bisabolene is a sesquiterpene and can be extracted from oregano and other aromatic plants. It may be a potential anticancer agent that can induce apoptosis in A549 cancer cell line.<br>References Grosso, N. R., et al.: Argent., Pat. Appl. AR 90961 A1 20141217 (2014); Yfanti, P., et al.: Am J Plant Sci. 6, 2092 (2015)<br></p>Formula:C15H24Purity:>85%Color and Shape:Colourless To Light YellowMolecular weight:204.35L-threo-Hex-2-enaric acid 1,4-Lactone
CAS:Formula:C6H6O7Color and Shape:Off-WhiteMolecular weight:190.11Deoxypyridinoline Chloride Trihydrochloride Salt
CAS:Controlled Product<p>Stability Hygroscopic<br>Applications Deoxypyridinoline Chloride Trihydrochloride Salt a collagen cross-links agent. A primary reference material for the monitoring of bone metabolism.<br>References Heaney, R., et al.: J. Bone Miner. Res., 5, 1135 (1990), Hannon, R., et al.: J. Bone Miner. Res., 13, 1124 (1998), Coudray, C., et al.: Eur. J. Nutr., 42, 91 (2003), Abrams, S., et al.: Am. J. Clin. Nutr., 82, 471 (2005),<br></p>Formula:C18H28N4O7·HClColor and Shape:NeatMolecular weight:448.899Calhex 231
CAS:Controlled Product<p>Applications A new calcium sensing receptor ligand demonstrating potent calcilytic activity.<br>References Ray, N., et al.: J. Bone Miner. Res., 12, 24 (1997), Sato, M., et al.: J. Med. Chem., 42, 1 (1999),Rodan, G., et al.: Science, 289, 1508 (2000), Goltzman, D., et al.: Nat. Rev. Drug Discov., 1, 784 (2002), Petrel, C., et al.: J. Biol. Chem., 279, 18990 (2004),<br></p>Formula:C25H27ClN2OColor and Shape:NeatMolecular weight:406.95Isopimaric Acid
CAS:Controlled Product<p>Applications A potent novel activators of large-conductance Ca2+-activated K+ channel.<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 Imaizumei, Y. et al.: Mol. Pharmacol., 62, 836 (2002); Chang, S. et al.: AM. J. Physiol., 298, F1416 (2010);<br></p>Formula:C20H30O2Purity:>90%Color and Shape:Off-WhiteMolecular weight:302.45GDC 0152
CAS:Controlled Product<p>Applications GDC 0152 is a peptidomimetic small molecule antagonist of inhibitor of apoptosis (IAP) proteins with antitumor activity.<br>References Yue, Q., et. al.: Drug Metab. Dispos., 41, 508 (2013)<br></p>Formula:C25H34N6O3SColor and Shape:NeatMolecular weight:498.64Di(a-tocopherol) Phosphate (>85%)
CAS:<p>Applications Di(α-tocopherol) Phosphate is used as a vitamin E supplement.<br>References Libinaki, R., et al.: Food Chem. Toxicol., 44, 916 (2006)<br></p>Formula:C58H99O6PPurity:>85%Color and Shape:NeatMolecular weight:923.382-O-a-D-Glucosylglycerol
CAS:Controlled Product<p>Stability Very Hygroscopic<br>Applications 2-O-α-D-Glucosylglycerol is used to prepare glycoglycerolipid analogs active as antitumor-promoters the influence of the anomeric configuration.<br>References Colombo, D., et al.: Eur. J. Med. Chem., 35, 1109 (2000);<br></p>Formula:C9H18O8Color and Shape:White To Off-WhiteMolecular weight:254.23N-[3-(N-L-Alanyl)-amino-3-carboxypropyl]-D-histidine Trihydrochloride
CAS:Controlled Product<p>Applications N-[3-(N-L-Alanyl)-amino-3-carboxypropyl]-D-histidine is an analog of Nicotianamine (N408500), a phytosiderophore that is produced in higher plants as iron chelating amino acids that promote uptake of iron from soil. Nicotianamine (N408500) biosynthesis in plants depicts the association of three enzymatic activities: a histidine racemase, an enzyme distantly related to nicotianamine synthase, and a staphylopine dehydrogenase belonging to the DUF2338 family.<br>References Klair, S., et al.: J. Plant Nutr., 19, 1295 (1996); Ghssein, G.; et al.: Science, 352, 1105 (2016)<br></p>Formula:C13H23Cl3N4O6Color and Shape:NeatMolecular weight:437.7N-Carboxy Ertapenem-d4 Di-(4-Nitrobenzyl) Ester
CAS:Controlled Product<p>Applications Intermediate in the preparation of Ertapenem (E635000).<br></p>Formula:C37D4H30N5NaO13SColor and Shape:NeatMolecular weight:815.7713a-Hydroxy Pravastatin-d3 Sodium Salt
CAS:Controlled Product<p>Stability Hygroscopic<br>Applications A metabolite of Pravastatin, a competitive inhibitor of HMG-CoA reductase. Bioactive metabolite of mevastatin.<br>References Serizawa, N., et al.: J. Antibiot., 36, 604 (1983), White, H.D, et al.: N. Engl. J. Med., 343, 317 (2000),<br></p>Formula:C23H32D3NaO7Color and Shape:NeatMolecular weight:449.53
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