
Indoles
Indoles are heterocyclic compounds composed of a benzene ring fused to a pyrrole ring. These compounds are important in medicinal chemistry for their wide range of biological activities, including anti-inflammatory, anticancer, and antimicrobial properties. Indoles are used in synthesizing pharmaceuticals, agrochemicals, and dyes. At CymitQuimica, we provide a comprehensive range of high-quality indoles for your research and industrial applications.
Subcategories of "Indoles"
Found 3983 products of "Indoles"
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2-(2-methyl-1H-indol-3-yl)-N-(thiophen-2-ylmethyl)ethan-1-amine hydrochloride
CAS:Purity:95.0%Molecular weight:306.8500061035156Ethyl 2-(2-(dimethylamino)pyrimidin-4-yl)-1H-indole-5-carboxylate
CAS:Purity:95.0%Molecular weight:310.35699462890625(3-Formyl-indol-1-yl)-acetic acid methyl ester
CAS:Formula:C12H11NO3Purity:95.0%Color and Shape:SolidMolecular weight:217.2243-(PYRROLIDIN-1-YLMETHYL)INDOLE
CAS:Purity:95.0%Color and Shape:SolidMolecular weight:200.28500366210938Methyl Indole-3-acetate
CAS:Controlled Product<p>Applications A phytohormone.<br>References Quittenden, L., et al.: Plant Physiol., 151, 1130 (2009), Jiraskova, D., et al.: J. Phycol., 45, 108 (2009),<br></p>Formula:C11H11NO2Color and Shape:Beige To Dark BrownMolecular weight:189.21(S)-1-Phenyl-1,2,3,4-tetrahydroisoquinoline
CAS:Controlled Product<p>Impurity Solifenacin EP impurity A<br>Applications Solifenacin (S676700) intermediate.<br>References Andersson, K., et al.: Drugs, 35, 477 (1988), Wallis, R., et al.: Life Sci., 64, 395 (1999), Mitsuya, M., et al.: J. Med. Chem., 43, 5017 (2000), Ohtake, A., et al.: Eur. J. Pharmacol., 492, 243 (2004),<br></p>Formula:C15H15NColor and Shape:White To Off-WhiteMolecular weight:209.29METHYL 4-BROMO-1-CYCLOPROPYL-1H-INDOLE-6-CARBOXYLATE
CAS:Purity:95.0%Molecular weight:294.14801025390625TERT-BUTYL 4-(1H-INDOL-1-YL)PIPERIDINE-1-CARBOXYLATE
CAS:Purity:95.0%Color and Shape:SolidMolecular weight:300.40200805664063-Methyl-d3-indole
CAS:Controlled Product<p>Applications 3-Methyl-d3-indole has been used to prove that bioactivation of the pulmonary toxin 3-methylindole requires methyl carbon-hydrogen bond breakage in mice. 3-Methyl-d3-indole is the labeled analogue of 3-Methylindole (M313470), A naturally abundant pneumotoxin, found primarily in mammalian feces providing its strong fecal odor.<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 Huijzer, J., et. al.: Toxicol. Appl. Pharm., 90, 60 (1987); Nakashima, T., et al.: Biol. Pharm. Bull., 32, 832 (2009); Xu, H., et al.: Chem. Pharm. Bull., 57, 321 (2009); Bodoor, K., et al.: J. Med. Chem., 52, 3753 (2009); Naskar, S., et al.: J. Chem. Res., 3, 174 (2009); Sollner, K., et al.: J. Agric. Food Chem., 57, 4319 (2009)<br></p>Formula:C92H3H6NColor and Shape:NeatMolecular weight:134.193-Methyl-1H-Indole-d8
CAS:Controlled Product<p>Applications 3-(methyl-d3)-1H-Indole-2,4,5,6,7-d5 is the labeled analogue of 3-Methylindole (M313470), a naturally abundant pneumotoxin, found primarily in mammalian feces providing its strong fecal odor; however in lower concentrations the compound has a pleasent aroma, giving orange blossoms and jasmine their pleasing scent. It is often a component of commercial fragrances and perfumes.<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 Nakashima, T., et al.: Biol. Pharm. Bull., 32, 832 (2009), Xu, H., et al.: Chem. Pharm. Bull., 57, 321 (2009), Bodoor, K., et al.: J. Med. Chem., 52, 3753 (2009), Naskar, S., et al.: J. Chem. Res., 3, 174 (2009), Sollner, K., et al.: J. Agric. Food Chem., 57, 4319 (2009),<br></p>Formula:C92H8HNColor and Shape:NeatMolecular weight:139.22Indoleacetic Acid
CAS:Controlled Product<p>Applications Indoleacetic Acid is the most common and naturally occuring plant hormone in the auxin class of hormones. It effects cell elongation, cell division as well as plant growth and development.<br></p>Formula:C10H9NO2Color and Shape:Off-White To Light BeigeMolecular weight:175.182-imino-4-(1H-indol-3-yl)-7,7-dimethyl-5-oxo-3,4,5,6,7,8-hexahydro-2H-1-benzopyran-3-carbonitrile
CAS:Purity:90%Molecular weight:333.39099121093754-(Bis(2-methyl-1H-indol-3-yl)methyl)-2-methoxyphenol
CAS:Purity:97%Molecular weight:396.4899902343751-benzyl-1H-indole-6-carbonitrile
CAS:Purity:95.0%Color and Shape:Liquid, No data available.Molecular weight:232.285995483398446-Benzyloxy-5-methoxy-1H-indole-2-carboxylic acid ethyl ester
Purity:95.0%Molecular weight:325.364013671875(2-{[2-(4-Fluorophenyl)-1H-indol-3-yl]thio}ethyl)amine
CAS:Purity:95.0%Molecular weight:286.36999511718756-Bromo-3-(2-chloro-5-(trifluoromethyl)pyrimidin-4-yl)-1-(phenylsulfonyl)-1H-indole
CAS:Purity:97%Molecular weight:516.719970703125(R)-5-Bromo-3-[(1-methyl-2-pyrrolidinyl)methyl]-1H-indole
CAS:Purity:95.0%Color and Shape:SolidMolecular weight:293.2080078125Aminorex
CAS:Controlled Product<p>Applications Aminorex is a metabolite of Levamisole (L331100). Aminorex is an anorectic stimulant drug of the 2-amino-5-aryl oxazoline class. Aminorex has been shown to have locomotor stimulant effects similar to Methamphetamine (M258795).<br>References Poos, G., et al.: J. Med. Chem., 6, 266 (1963), Watson, A., et al.: Res. Vet. Sci., 45, 411 (1988), Russell, B., et al.: Pharmacol. Biochem. Behav., 51, 375 (1995),<br></p>Formula:C9H10N2OColor and Shape:Off White SolidMolecular weight:162.19(2-{[2-(4-Methoxyphenyl)-1H-indol-3-yl]thio}ethyl)amine
CAS:Purity:95.0%Molecular weight:298.39999389648443-[(3-methyl-1,2,4-oxadiazol-5-yl)methyl]-1H-indole
CAS:Purity:95.0%Molecular weight:213.240005493164065-Benzyloxytryptamine hydrochloride
CAS:Purity:97.0%Color and Shape:Solid, Grey powderMolecular weight:302.79998779296875

