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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bis(furan-2-yl)methanone
CAS:<p>Bis(furan-2-yl)methanone is a furyl compound that is activated by trifluoromethanesulfonic acid. It has been shown to be an effective dose for the treatment of bacterial infections that are resistant to erythromycin and other antibiotics. Bis(furan-2-yl)methanone is used in veterinary medicine to treat infections caused by bacteria such as Escherichia coli, Proteus mirabilis, Klebsiella pneumoniae, and Streptococcus agalactiae. This drug has been shown to be active against Gram-positive bacteria, including Bacillus cereus, Clostridium perfringens, Clostridium tetani, Staphylococcus aureus, Streptococcus pyogenes, and Streptococcus pneumoniae.</p>Formula:C9H6O3Purezza:Min. 95%Peso molecolare:162.14 g/mol3-Methylenebicyclo[3.3.1]nonan-7-one
CAS:3-Methylenebicyclo[3.3.1]nonan-7-one is a chiral molecule that has been synthesized as a racemic mixture of two enantiomers. This compound is an amine with a hydroxy group and an isopropyl side chain. It has been shown to have anti-inflammatory properties, which may be due to its ability to inhibit cyclooxygenase and lipoxygenase activity. 3-Methylenebicyclo[3.3.1]nonan-7-one also has antiviral properties, which are due to its inhibition of protein synthesis in viruses by blocking the activity of ribonucleotide reductase, an enzyme required for nucleic acid synthesis. The reaction mechanism involves the formation of a covalent bond between the amantadine and the active site of ribonucleotide reductase through either radical or hydrogen atom transfer mechanisms.Formula:C10H14OPurezza:Min. 95%Peso molecolare:150.22 g/mol2-(3-Chloropropyl)pyridine hydrochloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C8H11Cl2NPurezza:Min. 95%Peso molecolare:192.08 g/mol4-Amino-2,3,6-trimethylphenol
CAS:<p>4-Amino-2,3,6-trimethylphenol (4ATMP) is a halogenated phenol that has been used as a developer in the production of silver halide photographic emulsions. It interacts with hydrogen chloride to form a gaseous product and can be used as an indicator for the presence of chlorine gas. 4ATMP is also known to react with formaldehyde and acetaldehyde to produce formic acid and acetic acid respectively. 4ATMP is most commonly prepared by reacting phenol with diethylaminopropyl chloride in the presence of hydrogen chloride gas.</p>Formula:C9H13NOPurezza:Min. 95%Peso molecolare:151.21 g/mol(2-Phenoxyethyl)amine hydrochloride
CAS:<p>2-Phenoxyethyl)amine hydrochloride is a chlorinated, industrial, synthetic chemical used as a reaction solvent. It can be derived from cyclohexylamine and ethanolamine by reacting with phenol. The reaction product is then hydrolyzed to produce 2-phenoxyethyl)amine hydrochloride.</p>Formula:C8H12ClNOPurezza:Min. 95%Peso molecolare:173.64 g/mol2,6-Dimethyl-2H-1,4-benzoxazin-3(4H)-one
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H11NO2Purezza:Min. 95%Peso molecolare:177.2 g/mol4-(Furan-2-yl)-4-oxobutanenitrile
CAS:<p>Versatile small molecule scaffold</p>Formula:C8H7NO2Purezza:Min. 95%Peso molecolare:149.15 g/mol3,7-Dibromo-1,5-naphthyridine
CAS:Versatile small molecule scaffoldFormula:C8H4Br2N2Purezza:Min. 95%Peso molecolare:287.94 g/mol3-Bromo-1,6-naphthyridine
CAS:<p>Versatile small molecule scaffold</p>Formula:C8H5BrN2Purezza:Min. 95%Peso molecolare:209.04 g/mol3,8-Dibromo-[1,6]naphthyridine
CAS:<p>Versatile small molecule scaffold</p>Formula:C8H4Br2N2Purezza:Min. 95%Peso molecolare:287.94 g/mol5-bromo-1,7-naphthyridine
CAS:<p>5-bromo-1,7-naphthyridine is a heterocyclic compound that can be derived from pyrrole by the introduction of an electron deficiency. This molecule has been shown to react with nucleophiles such as water and amide in order to yield unsaturated products. The molecule also has electron-donating groups on it, which can be used to optimize yields. 5-bromo-1,7-naphthyridine is often used as a reagent in organic synthesis.</p>Formula:C8H5BrN2Purezza:Min. 95%Peso molecolare:209 g/mol3,5-Dibromo-1,7-naphthyridine
CAS:Versatile small molecule scaffoldFormula:C8H4Br2N2Purezza:Min. 95%Peso molecolare:287.94 g/mol1,5-Naphthyridin-2-ylamine
CAS:<p>1,5-Naphthyridin-2-ylamine is a monocyclic heterocycle that is derived from the amination of 1,5-naphthyridine. It has been used in the preparation of amides and carbocycles. The reaction also produces nitro compounds. The naphthyridinone reacts with a variety of alkyl groups to produce either alkenyl or alkynyl groups. This reaction can be carried out on an industrial scale by using Grignard reagents. The reaction proceeds via a tautomerization mechanism to produce the desired products. It has been shown that this chemical is toxic to cells and can produce DNA damage.</p>Formula:C8H7N3Purezza:Min. 95%Peso molecolare:145.16 g/mol1,6-Naphthyridin-2-amine
CAS:<p>A 1,6-Naphthyridin-2-amine is a chemical compound that can be synthesized in various yields by extracting it from coal tar. It has been used in the past to make n-substituted derivatives for use in combinatorial and screening studies. A 1,6-Naphthyridin-2-amine can be synthesized using a microwave irradiation technique that uses malononitrile as its starting material. The microwave irradiation technique is operational at low temperatures and can be tracked with a radiotracer. Microwave irradiation of malononitrile produces an intermediate that reacts with ammonia to produce the desired 1,6-naphthyridinone product. This product can then be converted into the desired 1,6-naphthyridin-2 amine via hydrogenation or nitration.</p>Formula:C8H7N3Purezza:Min. 95%Peso molecolare:145.16 g/mol2-[2-(2,4-Dichlorophenyl)-1,3-thiazol-4-yl]acetic acid
CAS:Prodotto controllato2-[2-(2,4-Dichlorophenyl)-1,3-thiazol-4-yl]acetic acid is a small molecule inhibitor that belongs to the class of peptides. It inhibits protein interactions by binding to peptide receptors on the surface of cells. This inhibitor is used as a research tool for studying the function of receptor molecules. 2-[2-(2,4-Dichlorophenyl)-1,3-thiazol-4-yl]acetic acid has been shown to activate ligand and receptor interactions in vitro. The purity of this product is high and it can be used as a research tool in life science and ion channels.Formula:C11H7Cl2NO2SPurezza:Min. 95%Peso molecolare:288.1 g/molEthyl 2-carbamothioyl-2,2-dimethylacetate
CAS:Versatile small molecule scaffoldFormula:C7H13NO2SPurezza:Min. 95%Peso molecolare:175.25 g/mol2-Chloro-6-nitrobenzene-1-sulfonyl chloride
CAS:Versatile small molecule scaffoldFormula:C6H3Cl2NO4SPurezza:Min. 95%Peso molecolare:256.06 g/mol7-Bromo-5-phenyl-2,3,4,5-tetrahydro-1H-1,4-benzodiazepin-2-one
CAS:Prodotto controllato<p>Versatile small molecule scaffold</p>Formula:C15H13BrN2OPurezza:Min. 95%Peso molecolare:317.18 g/mol7-Methyl-5-phenyl-1,3,4,5-tetrahydro-2H-1,4-benzodiazepin-2-one
CAS:Prodotto controllato<p>Versatile small molecule scaffold</p>Formula:C16H16N2OPurezza:Min. 95%Peso molecolare:252.31 g/mol3-Oxocyclohexanecarbonitrile
CAS:3-Oxocyclohexanecarbonitrile (3OHC) is a novel chemical compound with analgesic properties. 3OHC has been shown to be effective in reducing the inflammation of the human body. The mechanism of action has not yet been elucidated, but it may be due to its ability to inhibit prostaglandin synthesis and reduce the oxidative stress by forming reactive oxygen species. 3OHC is also an active antinociceptive agent that can be used in combination with other drugs to treat inflammatory diseases. 3OHC is able to reduce the pain caused by inflammatory diseases by reducing the production of prostaglandins, which are a group of chemicals that are responsible for causing pain and inflammation.Formula:C7H9NOPurezza:Min. 95%Peso molecolare:123.15 g/mol
