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(1.243 prodotti)
- Building Blocks Idrocarburici(6.097 prodotti)
- Building Blocks organici(61.045 prodotti)
Trovati 203842 prodotti di "Building Blocks"
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3-Cyclopropylimidazolidine-2,4-dione
CAS:<p>Versatile small molecule scaffold</p>Formula:C6H8N2O2Purezza:Min. 95%Peso molecolare:140.14 g/molPhenyl morpholine-4-carboxylate
CAS:Versatile small molecule scaffoldFormula:C11H13NO3Purezza:Min. 95%Peso molecolare:207.23 g/molN-(5-Aminopyridin-2-yl)benzamide
CAS:<p>Versatile small molecule scaffold</p>Formula:C12H11N3OPurezza:Min. 95%Peso molecolare:213.23 g/molN-(4-Methoxybenzyl)-4-methyl-1,2,3-thiadiazole-5-carboxamide
CAS:Versatile small molecule scaffoldFormula:C12H13N3O2SPurezza:Min. 95%Peso molecolare:263.32 g/mol3-Bromo-3-methylpyrrolidine-2,5-dione
CAS:Versatile small molecule scaffoldFormula:C5H6BrNO2Purezza:Min. 95%Peso molecolare:192.01 g/mol2-(5-Bromo-2-methoxyphenyl)pyrrolidine
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H14BrNOPurezza:Min. 95%Peso molecolare:256.14 g/mol1-(1-Bromoethyl)-2-nitrobenzene
CAS:Versatile small molecule scaffoldFormula:C8H8BrNO2Purezza:Min. 95%Peso molecolare:230.06 g/molPentacyclo[6.3.0.0(2,7).0(4,11).0(5,9)]undecan-3-one
CAS:Pentacyclo[6.3.0.0(2,7).0(4,11).0(5,9)]undecan-3-one is a polycyclic compound that has been postulated to be a thione derived from the desulfurization of pentacyclo[6.3.0.0(2,7).0(4,11).0(5,9)]undecane with dimethoxycarbene and toluene as reagents in the presence of a catalyst (Scheme 1). The stereoselective desulfurization of the lactams leads to the formation of either (1S) or (1R) products depending on the conditions used for the reaction. This reaction is thermally driven and occurs at 130°C under vacuum with a pressure of 10-2 Torr. The desulfurized product can then be converted into various esters by treatment with alcohols in the presence ofFormula:C11H12OPurezza:Min. 95%Peso molecolare:160.21 g/mol3-(Chloromethyl)-1H-pyrazole hydrochloride
CAS:Versatile small molecule scaffoldFormula:C4H6Cl2N2Purezza:Min. 95%Peso molecolare:153.01 g/mol3-Methyl-3,6-diazabicyclo[3.2.1]octane
CAS:Versatile small molecule scaffoldFormula:C7H14N2Purezza:Min. 95%Peso molecolare:126.2 g/mol2-Hydroxy-2-methyl-1-[4-(propan-2-yl)phenyl]propan-1-one
CAS:Versatile small molecule scaffoldFormula:C13H18O2Purezza:Min. 95%Peso molecolare:206.28 g/mol6-Bromo-4-methylquinazoline
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H7BrN2Purezza:Min. 95%Peso molecolare:223.07 g/mol4-(4-Fluorophenyl)-1,2,3,6-tetrahydro-1-methylpyridine
CAS:4-(4-Fluorophenyl)-1,2,3,6-tetrahydro-1-methylpyridine is a chemical substance that can be used in the preparation of samples for analysis. It is sensitive to paroxetine and has analytical properties that are suitable for use as an analytical standard. 4-(4-Fluorophenyl)-1,2,3,6-tetrahydro-1-methylpyridine has been validated using liquid chromatography coupled with tandem mass spectrometry (LC/MS/MS) and has been shown to be minimal and highly repeatable. This reagent can be used in environments where the presence of toxic substances is not desirable.Formula:C12H14FNPurezza:Min. 95%Peso molecolare:191.24 g/mol(2-Amino-5-methylphenyl)phosphonic acid
CAS:Versatile small molecule scaffoldFormula:C7H10NO3PPurezza:Min. 95%Peso molecolare:187.13 g/mol2-[2-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)ethoxy]acetic acid
CAS:<p>2-[2-(1,3-Dioxo-2,3-dihydro-1H-isoindol-2-yl)ethoxy]acetic acid is an analog of niacinamide. It is a colorless liquid at room temperature and has a chemical formula of C5H8O4. 2-[2-(1,3-Dioxo-2,3-dihydro-1H-isoindol-2-yl)ethoxy]acetic acid can be synthesized by reacting ethyl acetate with acetone and methyl ethyl ketone. This reaction produces a mixture of diacetates. The diacetates are then reacted with nitric acid to produce 2-[2-(1,3-dioxo-2,3,-dihydroisindol)-2yl)ethoxy]acetic acid. The synthesis of this compound is similar to the synthesis of niacinamide from</p>Formula:C12H11NO5Purezza:Min. 95%Peso molecolare:249.22 g/mol3-(Pyridin-3-yl)-4,5-dihydro-1H-pyrazol-5-one
CAS:Versatile small molecule scaffoldFormula:C8H7N3OPurezza:Min. 95%Peso molecolare:161.16 g/molrac-(2R,4R,6S)-2,4,6-Trimethylpiperidine hydrochloride
CAS:Versatile small molecule scaffoldFormula:C8H18ClNPurezza:Min. 95%Peso molecolare:163.69 g/molMethyl 2-chloro-2-methyl-3-phenylpropanoate
CAS:Versatile small molecule scaffoldFormula:C11H13ClO2Purezza:Min. 95%Peso molecolare:212.67 g/molDimethyl-1,3-oxazole-5-carbonyl chloride
CAS:Versatile small molecule scaffoldFormula:C6H6ClNO2Purezza:Min. 95%Peso molecolare:159.57 g/mol5-bromo-4-chloro-2,6-dimethylpyrimidine
CAS:Versatile small molecule scaffoldFormula:C6H6BrClN2Purezza:Min. 95%Peso molecolare:221.5 g/mol
![Pentacyclo[6.3.0.0(2,7).0(4,11).0(5,9)]undecan-3-one](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FUCA64919.webp&w=3840&q=75)
![3-Methyl-3,6-diazabicyclo[3.2.1]octane](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FUCA66709.webp&w=3840&q=75)
![2-Hydroxy-2-methyl-1-[4-(propan-2-yl)phenyl]propan-1-one](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FUCA67385.webp&w=3840&q=75)
![2-[2-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)ethoxy]acetic acid](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FUCA67665.webp&w=3840&q=75)
