Building Blocks
Questa sezione contiene prodotti fondamentali per la sintesi di composti organici e biologici. Building blocks sono i materiali di partenza essenziali utilizzati per costruire molecole complesse attraverso varie reazioni chimiche. Svolgono un ruolo critico nella scoperta di farmaci, nella scienza dei materiali e nella ricerca chimica. Presso CymitQuimica, offriamo una gamma diversificata di building blocks di alta qualità per supportare le tue ricerche innovative e progetti industriali, assicurandoti di avere i componenti essenziali per una sintesi di successo.
Sottocategorie di "Building Blocks"
- Acidi boronici e derivati dell'acido boronico(5.778 prodotti)
- Building Blocks Chirali(1.242 prodotti)
- Building Blocks Idrocarburici(6.098 prodotti)
- Building Blocks organici(61.059 prodotti)
Trovati 199580 prodotti di "Building Blocks"
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2-Chloro-N-(2-{5-[(4-ethoxyphenyl)methylidene]-2,4-dioxo-1,3-thiazolidin-3-yl}ethyl)acetamide
CAS:<p>Versatile small molecule scaffold</p>Formula:C16H17ClN2O4SPurezza:Min. 95%Peso molecolare:368.8 g/molCycloheptyl isothiocyanate
CAS:<p>Cycloheptyl isothiocyanate is a 1-4c alkyl, azaheterocycle, isothiocyanate that has been shown to be stereoselective. It binds to the sulfur atom of thiols and sulfonylureas, preventing the formation of the reactive intermediate that leads to their hydrolysis. This property can be used for the synthesis of ensembles and aralkyls. Cycloheptyl isothiocyanate also binds to alkenyl groups, which may be useful in synthesizing cycloalkyls or haloalkyls.</p>Formula:C8H13NSPurezza:Min. 95%Peso molecolare:155.26 g/mol3-(4-Chloro-3-nitrobenzenesulfonamido)propanoic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H9ClN2O6SPurezza:Min. 95%Peso molecolare:308.7 g/mol1-{6-Oxa-3-azabicyclo[3.1.0]hexan-3-yl}ethan-1-one
CAS:<p>Versatile small molecule scaffold</p>Formula:C6H9NO2Purezza:Min. 95%Peso molecolare:127.14 g/moltert-Butyl 2-(hydroxymethyl)-4H,5H,6H,7H-[1,3]thiazolo[4,5-c]pyridine-5-carboxylate
CAS:<p>Versatile small molecule scaffold</p>Formula:C12H18N2O3SPurezza:Min. 95%Peso molecolare:270.35 g/mol2,3,3-Trimethylbicyclo[2.2.1]heptane-2-carboxylic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H18O2Purezza:Min. 95%Peso molecolare:182.3 g/mol6-(3-Methylbutoxy)pyridazin-3-amine
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H15N3OPurezza:Min. 95%Peso molecolare:181.23 g/mol1-(3-Methyl-isothiazol-5-yl)-ethanone
CAS:<p>Versatile small molecule scaffold</p>Formula:C6H7NOSPurezza:Min. 95%Peso molecolare:141.19 g/mol2,2-Diethyl-4-methoxy-4-oxobutanoic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H16O4Purezza:Min. 95%Peso molecolare:188.22 g/mol7-(Bromomethyl)-6-oxaspiro[3.5]nonane
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H15BrOPurezza:Min. 95%Peso molecolare:219.12 g/molEthyl 2-hydroxy-3-phenylpropanoate
CAS:<p>Ethyl 2-hydroxy-3-phenylpropanoate (EPP) is a component of the fragrance, which is used in perfumes, soaps, and detergents. It has been shown to have a hypocholesterolemic effect in rats and a proliferator-activated receptor agonist effect on human cells. EPP also has been shown to stimulate collagen production and inhibit the proliferation of human keratinocytes. The biological properties of this compound are related to its ability to activate insulin receptors in muscle cells. EP can be synthesized by reacting 3-phenylpropanal with ethyl bromoacetate followed by hydrolysis of the resulting ester.</p>Formula:C11H14O3Purezza:Min. 95%Peso molecolare:194.23 g/mol4-[(tert-Butoxy)methyl]aniline
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H17NOPurezza:Min. 95%Peso molecolare:179.26 g/mol[2-(4-Methylphenoxy)phenyl]methanamine
CAS:<p>Versatile small molecule scaffold</p>Formula:C14H15NOPurezza:Min. 95%Peso molecolare:213.27 g/mol4-Amino-2-methylcyclohexan-1-ol
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H15NOPurezza:Min. 95%Peso molecolare:129.2 g/mol(1H-Pyrazol-4-yl)-acetic acid methyl ester hydrochloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C6H9ClN2O2Purezza:Min. 95%Peso molecolare:176.6 g/mol1-[3-(Dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydro-3-oxo-5-isobenzofurancarbonitrile
CAS:<p>Please enquire for more information about 1-[3-(Dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydro-3-oxo-5-isobenzofurancarbonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C20H19FN2O2Purezza:Min. 95%Peso molecolare:338.38 g/mol5,6-Dibromopyridin-2-ol
CAS:<p>Versatile small molecule scaffold</p>Formula:C5H3Br2NOPurezza:Min. 95%Peso molecolare:252.89 g/mol2-Acetylbenzoic acid
CAS:<p>2-Acetylbenzoic acid is a functional molecule that contains an acetyl group. It can form hydrogen bonds with other molecules and has been shown to induce apoptosis in cells. The reaction products of 2-acetylbenzoic acid are malonic acid, acetylsalicylic acid, and 2-benzoylbenzoic acid. These three compounds are made by the addition of hydrogen or hydroxide to the molecule 2-acetylbenzoic acid. The molecule has two functional groups: a carbonyl group and an acetyl group. The chemical structure of this molecule can be seen in the figure below.<br>2-Acetylbenzoic Acid</p>Formula:C9H8O3Purezza:Min. 95%Colore e forma:PowderPeso molecolare:164.16 g/molRef: 3D-FA05086
Prodotto fuori produzionetert-Butyl 5-bromo-3,4-dihydro-2,7-naphthyridine-2(1H)-carboxylate
CAS:<p>Versatile small molecule scaffold</p>Formula:C13H17BrN2O2Purezza:Min. 95%Peso molecolare:313.19 g/mol2-Bromo-3,3,3-trifluoro-1-propene
CAS:Prodotto controllato<p>2-Bromo-3,3,3-trifluoro-1-propene is a chemical compound that has been synthesized in an asymmetric reaction. The reactant is bromopropane and the product is 2,2,2-trifluoropropene. The methylene group on the propene molecule is activated by the nucleophilic attack of a fluoride ion from hydrogen fluoride to form a cavity with a highly strained bond. The kinetic study of this reaction revealed that the activation energy for the reaction is 42 kJ/mol. Palladium-catalyzed coupling reactions are catalyzed by palladium and require nonpolar solvents such as toluene or dichloromethane. This type of reaction has been shown to be exothermic with an isolated yield of 1%.</p>Formula:C3H2BrF3Purezza:Min. 95%Colore e forma:Colorless PowderPeso molecolare:174.95 g/mol4-(Methylamino)benzene-1-sulfonamide
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H10N2O2SPurezza:Min. 95%Peso molecolare:186.23 g/mol2,2',4,4'-tetrahydroxybenzophenone
CAS:<p>2,2',4,4'-tetrahydroxybenzophenone is a hydroxylated benzophenone that has immunomodulatory effects. It binds to the receptor in the immune system and can cause an increase in cytokine production. 2,2',4,4'-tetrahydroxybenzophenone is cytotoxic and has significant toxicity in vitro. The molecule has been shown to disrupt mitochondrial membrane potential. This may be due to its ability to form hydrogen bonds with molecules on the mitochondrial membrane. 2,2',4,4'-tetrahydroxybenzophenone also modulates transcriptional regulation of genes involved in cell proliferation and apoptosis. The drug is detectable at low levels by mass spectrometry and is not known to have any toxicological effects.END>></p>Formula:C13H10O5Purezza:Min. 95%Colore e forma:Green PowderPeso molecolare:246.22 g/molRef: 3D-FT55663
Prodotto fuori produzione3-Methylbenzo[b]thiophene-2-carboxylic acid
CAS:<p>3-Methylbenzo[b]thiophene-2-carboxylic acid (MBTCA) is a heterocyclic compound that is an intermediate in the synthesis of 3-methylthiophene-2-carboxylic acid, a precursor to other drugs. MBTCA is an aerobic, nonpolar compound that has shown antimicrobial activity against some bacteria and fungi. It also has been shown to have practicality as a biomolecular probe for methyl groups in organic solvents. MBTCA can be synthesized by nitration of benzene in the presence of sulfur and sulfoxides. This reaction produces nitrobenzene, which can then be oxidized by potassium permanganate or hydrogen peroxide to produce MBTCA. The most common isomer of MBTCA is 2-(3,5-dimethoxybenzylidene)tetrahydrofuran, with three methyl groups on the</p>Formula:C10H8O2SPurezza:Min. 95%Peso molecolare:192.23 g/mol3-amino-6-bromopyridin-2-ol hydrobromide
CAS:<p>Versatile small molecule scaffold</p>Formula:C5H6Br2N2OPurezza:Min. 95%Peso molecolare:269.9 g/mol3-[5-(Aminomethyl)-1-oxo-2,3-dihydro-1H-isoindol-2-yl]piperidine-2,6-dione hydrochloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C14H16ClN3O3Purezza:Min. 95%Peso molecolare:309.75 g/mol(2S,3R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-methoxybutanoic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C20H21NO5Purezza:Min. 95%Peso molecolare:355.4 g/mol2-Phenoxyaniline
CAS:<p>2-Phenoxyaniline is a nitro compound that can be converted to the corresponding palladium complexes. It is an inhibitor of the acylation reaction, which is a type of chemical reaction in which an organic molecule reacts with an acid. The inhibition of this reaction has been shown to have an effect on heart disease, specifically by lowering cholesterol levels and reducing atherosclerosis. 2-Phenoxyaniline has also been shown to inhibit the activation energy for electron transfer reactions, making it useful as a catalyst in analytical methods. 2-Phenoxyaniline also undergoes vibrational spectroscopy when exposed to liquid chromatography and other analytical methods.</p>Formula:C12H11NOPurezza:Min. 95%Colore e forma:Brown PowderPeso molecolare:185.22 g/mol3-(Methoxycarbonyl)pyridine-4-carboxylic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C8H7NO4Purezza:Min. 95%Peso molecolare:181.15 g/molH-Ser-Ala-Glu-Glu-Tyr-Glu-Tyr-Pro-Ser OH trifluoroacetate
CAS:<p>Please enquire for more information about H-Ser-Ala-Glu-Glu-Tyr-Glu-Tyr-Pro-Ser OH trifluoroacetate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C47H63N9O20•(C2HF3O2)xPurezza:Min. 95%Ref: 3D-FS183525
Prodotto fuori produzioneGivinostat hydrochloride
CAS:<p>Givinostat hydrochloride is a research chemical that has shown potential in various fields. It is a molybdenum-based compound that has been studied for its effects on dopamine release and hydrogen evolution. Givinostat hydrochloride has also been investigated as an osteoclast inhibitor, which may be beneficial in the treatment of bone-related disorders such as osteoporosis. Additionally, it has shown promise as a retinoid and calpain inhibitor, suggesting its potential use in dermatological conditions and neurodegenerative diseases. The compound contains fluorine atoms, making it suitable for imaging studies using fluorine MRI techniques. Givinostat hydrochloride has been tested on MDA-MB-231 cells and has shown inhibitory effects on their growth, indicating its potential as an anticancer agent.</p>Formula:C24H27N3O4·HClPurezza:Min. 95%Peso molecolare:457.95 g/mol
