Building Blocks
Esta sección contiene productos fundamentales para la síntesis de compuestos orgánicos y biológicos. Building blocks son los materiales de partida esenciales utilizados para construir moléculas complejas a través de diversas reacciones químicas. Desempeñan un papel crítico en el descubrimiento de fármacos, la ciencia de materiales y la investigación química. En CymitQuimica, ofrecemos una gama diversa de building blocks de alta calidad para apoyar sus investigaciones innovadoras y proyectos industriales, asegurando que tenga los componentes esenciales para una síntesis exitosa.
Subcategorías de "Building Blocks"
- Ácidos borónicos y derivados del ácido borónico(5.756 productos)
- Building Blocks quirales(1.242 productos)
- Building Blocks de hidrocarburos(6.095 productos)
- Building Blocks orgánicos(61.038 productos)
Se han encontrado 196817 productos de "Building Blocks"
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
CASIN
CAS:<p>CASIN is a lysine-derived antimicrobial agent that inhibits the growth of bacteria by binding to the peptide chains of collagen, which are found in skin and mucous membranes. CASIN has been shown to inhibit the growth of many bacterial species, including those that are resistant to other antibiotics. CASIN can be used for the treatment of infectious diseases caused by bacteria, such as bacterial vaginosis or chlamydia. CASIN has also been shown to reduce body mass index in animal models. The mechanism of action is not known but may involve interference with an enzyme that controls the biosynthesis of fatty acids. The use of CASIN in humans is limited due to its toxicity on human cells and potential safety concerns.</p>Fórmula:C20H22N2OPureza:Min. 95%Peso molecular:306.4 g/moltert-Butyl N-[3-(tetramethyl-1,3,2-dioxaborolan-2-yl)propyl]carbamate
CAS:<p>Versatile small molecule scaffold</p>Fórmula:C14H28BNO4Pureza:Min. 95%Peso molecular:285.19 g/molLeu-Leu-Leu-OH
CAS:<p>Leu-Leu-Leu-OH is a pentapeptide that is used in cancer treatment to inhibit the growth of cancer cells. It prevents the production of proteins and, as a result, cell division. Leu-Leu-Leu-OH has been shown to be effective against tumor cells with an antibody that binds to the surface of cells. The monoclonal antibody is taken up by the cancer cells through receptor mediated endocytosis, which leads to inhibition of protein synthesis and cell death.</p>Fórmula:C18H35N3O4Pureza:Min. 95%Forma y color:White PowderPeso molecular:357.49 g/molmethyl 4-bromo-3-formylbenzoate
CAS:<p>Versatile small molecule scaffold</p>Fórmula:C9H7BrO3Pureza:Min. 95%Peso molecular:243.1 g/molBenzyl N,N,N',N'-Tetraisopropylphosphorodiamidite
CAS:<p>Benzyl N,N,N',N'-tetraisopropylphosphorodiamidite is a reagent that reacts with hydroxybenzyl amine to form an ester. This product is used for the synthesis of phosphoramidites and benzyl esters. It is also used as a catalyst for the synthesis of diesters.</p>Fórmula:C19H35N2OPPureza:Min. 95%Peso molecular:338.48 g/molMethacryloxypropyl terminated polydimethylsiloxanes
CAS:<p>MW 20,000 - 30,000</p>Fórmula:C20H40O6Si3Pureza:Min. 95%Peso molecular:460.8 g/mol7-Fluoroisoquinolin-1-amine
CAS:<p>Versatile small molecule scaffold</p>Fórmula:C9H7FN2Pureza:Min. 95%Peso molecular:162.16 g/mol4-Amino-3-isothiazolidinone 1,1-dioxide hydrochloride
CAS:Versatile small molecule scaffoldFórmula:C3H7ClN2O3SPureza:Min. 95%Peso molecular:186.62 g/mol2-Mercaptopyridine
CAS:<p>2-Mercaptopyridine is a quinone that has been used as an inhibitor of the HIV reverse transcriptase enzyme. It binds to the active site of the enzyme and inhibits its activity by forming a stable covalent bond with two cysteine residues in the enzyme. The molecule is stabilized by two adjacent sulfide bonds, which form a six-membered ring with three nitrogen atoms and one oxygen atom. This ring coordinates to the zinc ion in the active site of the enzyme. 2-Mercaptopyridine has also been found to be effective against methicillin-resistant Staphylococcus aureus (MRSA) and Mycobacterium tuberculosis. 2-Mercaptopyridine binds to DNA at positions where it is complementary to guanine or adenine nucleotides, thus preventing RNA synthesis and replication.</p>Fórmula:C5H5NSPureza:Min. 95%Forma y color:PowderPeso molecular:111.17 g/mol2-Bromo-4-iodoanisole
CAS:<p>2-Bromo-4-iodoanisole is an electrophilic intermediate that can be synthetically prepared by regioselective halogenations of 4-iodoanisole. It is also a substrate for sequential halogenations with bromine or iodine. The 2-bromo-4-iodoanisole reacts with aluminum to form an aluminate, which can be used as a catalyst in organic synthesis. 2-Bromo-4-iodoanisole has been shown to react with aromatic rings by electrophilically attacking the ring and adding a second bromine atom to the ring, leading to quenching of the molecule and formation of structurally diverse products.</p>Fórmula:C7H6BrIOPureza:Min. 95%Peso molecular:312.93 g/mol2-[3-Chloro-5-(trifluoromethyl)-2-pyridinyl]-acetonitrile
CAS:<p>Versatile small molecule scaffold</p>Fórmula:C8H4ClF3N2Pureza:Min. 95%Forma y color:PowderPeso molecular:220.58 g/mol1,3,5,7-Tetrabromoadamantane
CAS:<p>1,3,5,7-Tetrabromoadamantane is a molecule that has been synthesized and introduced as a mediator to introduce oxidants. The introduction of the oxidant is mediated by 1,3,5,7-tetrabromoadamantane. This molecule has been shown to be synthesized in two steps from hexamethylenetetramine (HMT) and iodomethane. The synthesis of this molecule can also be achieved by reacting synthons such as tetraphenylmethane with hydrochloric acid. 1,3,5,7-Tetrabromoadamantane is an equivalence mediator because it can mediate a redox reaction in which the oxidizing agent is reduced and the reducing agent is oxidized.</p>Fórmula:C10H12Br4Pureza:Min. 95%Peso molecular:451.82 g/molN-(4-Bromophenyl)-N-phenylacrylamide
CAS:<p>Versatile small molecule scaffold</p>Fórmula:C15H12BrNOPureza:Min. 95%Forma y color:PowderPeso molecular:302.16 g/molMethyl 4-amino-2-methoxybenzoate
CAS:<p>Methyl 4-amino-2-methoxybenzoate is a solute with anticancer activity. It has been shown to inhibit the growth of erythrocytes and cancer cells in vitro. The mechanism of action is associated with its ability to bind to aminobenzothiazole, which inhibits the production of DNA and RNA. Methyl 4-amino-2-methoxybenzoate has also been shown to inhibit the proliferation of human muscle cells and induce their differentiation. This drug does not have any effect on lipid or protein synthesis in cells, which may be due to its solvent perturbation properties.</p>Fórmula:C9H11NO3Pureza:Min. 95%Forma y color:PowderPeso molecular:181.19 g/molFerrocenylmethyl methacrylate
CAS:<p>Ferrocenylmethyl methacrylate is a reactive, irreversible oxidation agent. It is used in the synthesis of hydroxylated polymers and redox-active biological sensors. Ferrocenylmethyl methacrylate has been used as a component in polymerization reactions to produce polymers with recording potential. It has also been used for the detection of cancer cells and for the diagnosis of prostate cancer.</p>Fórmula:C15H16FeO2Pureza:Min. 95%Peso molecular:284.13 g/mol4-Bromo-2,5-dimethoxybenzaldehyde
CAS:<p>4-Bromo-2,5-dimethoxybenzaldehyde is a nucleophilic compound that can act as an iminium. It is used in the synthesis of chalcones, which are aromatic compounds that have been found to have anticancer properties. 4-Bromo-2,5-dimethoxybenzaldehyde has two isomers: 2,4-dimethoxybenzaldehyde and 2,5-dimethoxybenzaldehyde. The separation of these compounds can be achieved using chromatography with a silica gel column. This process can be done on both the mixture of the two isomers or on one specific isomer. The synthetic pathway for this product begins with benzylpiperazine and piperazine. These two molecules react to form 3,4-dichlorobenzylpiperazine, which reacts with dimethoxybenzyl chloride to form 4-bromo-2,5-dim</p>Fórmula:C9H9BrO3Pureza:Min. 95%Peso molecular:245.07 g/mol2,6-Dimethoxyisonicotinic acid
CAS:<p>2,6-Dimethoxyisonicotinic acid is a cytotoxic agent that is structurally related to colchicine and combretastatin A-4. It has been shown to induce apoptosis in cancer cells by inhibiting the polymerization of tubulin. This drug also inhibits the proliferation of cancer cells by binding to DNA and disrupting the synthesis of proteins necessary for cell division. The inhibitory effect on protein synthesis may be due to its ability to inhibit the activity of RNA polymerase II and III, which are essential for transcription. 2,6-Dimethoxyisonicotinic acid also induces an anticancer effect through its ability to bind to phenolic moieties and inhibit the growth of cancer cells.</p>Fórmula:C8H9NO4Pureza:Min. 95%Peso molecular:183.16 g/molSodium 4-hydroxybenzenesulfonate dihydrate
CAS:<p>Sodium 4-hydroxybenzenesulfonate dihydrate is a hydrogenated compound with reactive properties. It is used in the production of optical materials and is used to produce hydrogen peroxide, which is a strong oxidizing agent. Sodium 4-hydroxybenzenesulfonate dihydrate has been shown to react with calcium ions to form calcium sulfinates. The luminescence property of this compound can be enhanced by mixing it with other compounds such as x-ray diffraction study, functional groups, or hydrogen peroxide. The reaction time for the formation of sodium 4-hydroxybenzenesulfonate dihydrate can be shortened by adding anions such as sulfamic acid.</p>Fórmula:C6H5NaO4S·2H2OPureza:Min. 95%Forma y color:White To Off-White SolidPeso molecular:232.19 g/moltert-Butyl 3-(piperidin-3-yl)azetidine-1-carboxylate
CAS:<p>Versatile small molecule scaffold</p>Fórmula:C13H24N2O2Pureza:Min. 95%Peso molecular:240.35 g/mol(1R,4R)-2-Oxa-5-azabicyclo[2.2.1]heptane hydrochloride
CAS:<p>Versatile small molecule scaffold</p>Fórmula:C5H9NO·HClPureza:Min. 95%Peso molecular:135.59 g/mol
