Building Blocks
Subcategorías de "Building Blocks"
- Ácidos borónicos y derivados del ácido borónico(5.775 productos)
- Building Blocks quirales(1.238 productos)
- Building Blocks de hidrocarburos(6.099 productos)
- Building Blocks orgánicos(60.996 productos)
Se han encontrado 205207 productos de "Building Blocks"
Cyanidin 3-O-rutinoside
CAS:Please enquire for more information about Cyanidin 3-O-rutinoside including the price, delivery time and more detailed product information at the technical inquiry form on this pageFórmula:C27H31O15Pureza:Min. 95%Peso molecular:595.53 g/molCoproporphyrin III
CAS:Please enquire for more information about Coproporphyrin III including the price, delivery time and more detailed product information at the technical inquiry form on this page
Fórmula:C36H38N4O8Pureza:Min. 95%Peso molecular:654.71 g/mol4-Chloro-N-[2-(1,2-dihydro-2-oxo-4-quinolinyl)ethyl]benzamide
CAS:Please enquire for more information about 4-Chloro-N-[2-(1,2-dihydro-2-oxo-4-quinolinyl)ethyl]benzamide including the price, delivery time and more detailed product information at the technical inquiry form on this page
Fórmula:C18H15ClN2O2Pureza:Min. 95%Peso molecular:326.78 g/mol(αR)-α-(2-Chlorophenyl)-2H-tetrazole-2-ethanol
CAS:Please enquire for more information about (αR)-α-(2-Chlorophenyl)-2H-tetrazole-2-ethanol including the price, delivery time and more detailed product information at the technical inquiry form on this page
Fórmula:C9H9ClN4OPureza:Min. 95%Peso molecular:224.65 g/molD-Carnosine trifluoroacetate
CAS:Please enquire for more information about D-Carnosine trifluoroacetate including the price, delivery time and more detailed product information at the technical inquiry form on this page
Fórmula:C9H14N4O3•(C2HF3O2)xPureza:Min. 95%N-[2-[(2S)-2-Cyano-4,4-difluoro-1-pyrrolidinyl]-2-oxoethyl]-6-[methyl[3-(1-piperazinyl)propyl]amino]-4-quinolinecarboxamide trifluor oacetate
CAS:Please enquire for more information about N-[2-[(2S)-2-Cyano-4,4-difluoro-1-pyrrolidinyl]-2-oxoethyl]-6-[methyl[3-(1-piperazinyl)propyl]amino]-4-quinolinecarboxamide trifluor oacetate including the price, delivery time and more detailed product information at the technical inquiry form on this pageFórmula:C25H31F2N7O2•(C2HF3O2)xPureza:Min. 95%Peso molecular:499.56 g/mol(1R,5S,6r)-rel-3-Oxabicyclo[3.1.0]hexane-6-carboxylic acid
CAS:Versatile small molecule scaffoldFórmula:C6H8O3Pureza:Min. 95%Peso molecular:128.13 g/mol2,6-Dichloro-4-methoxyaniline
CAS:2,6-Dichloro-4-methoxyaniline is a chemical that belongs to the group of methyl derivatives. It is used as an industrial chemical and as a precursor to other chemicals in the production of pesticides, herbicides, and other products. 2,6-Dichloro-4-methoxyaniline can be found in brominated flame retardants and phenolic resins. It is also present in pentachlorophenol (PCP) and hydroxylated congeners. 2,6-Dichloro-4-methoxyaniline has been detected in humans at levels ranging from 10 to 100 parts per billion. The chemical structure of 2,6-dichloro-4-methoxyaniline is similar to that of triclosan, which has been shown to have antimicrobial activity against bacteria such as Staphylococcus aureus and EscherichFórmula:C7H7Cl2NOPureza:Min. 95%Peso molecular:192.04 g/mol2,4-Dichloropyrido [2,3-D] pyrimidine
CAS:2,4-Dichloropyrido [2,3-D] pyrimidine is a regioselective chlorination agent that can be used for the synthesis of various organic compounds. It is often used in cross-coupling reactions to form carbon-carbon bonds. 2,4-Dichloropyrido [2,3-D] pyrimidine has been shown to give high yields and is selective for disubstituted or monosubstituted substrates. This compound is also useful for the functionalization of C-H bonds via palladium-catalyzed coupling reactions.
Fórmula:C7H3Cl2N3Pureza:Min. 95%Forma y color:White PowderPeso molecular:200.02 g/mol2-[(6-Chloro-3,4-dihydro-3-methyl-2,4-dioxo-1(2H)-pyrimidinyl)methyl]-benzonitrile
CAS:2-[(6-Chloro-3,4-dihydro-3-methyl-2,4-dioxo-1(2H)-pyrimidinyl)methyl]-benzonitrile is an antibacterial agent that belongs to the group of nitro compounds. It inhibits bacterial growth by blocking the synthesis of proteins and DNA. 2-[(6-Chloro-3,4-dihydro-3-methyl-2,4-dioxo-1(2H)-pyrimidinyl)methyl]-benzonitrile has been shown to be active against a wide range of bacteria including Gram positive and Gram negative organisms. This compound also exhibits metal ion chelating properties and can be used for the removal of heavy metals from water. The square planar geometry of 2-[(6-Chloro-3,4-(dihydro)-3-(methyl)-2,4-(dioxo)-1Fórmula:C13H10ClN3O2Pureza:Min. 95%Peso molecular:275.69 g/mol3,5-Diiodo-L-tyrosine
CAS:3,5-Diiodo-L-tyrosine (3DILT) is an iodinated amino acid that can be used as a marker for human immunodeficiency virus (HIV) infection. It is synthesized by the reaction of 3,5-diiodotyrosine with L-tyrosine in the presence of a metal chelate and dinucleotide phosphate. This reaction proceeds via nucleophilic substitution on the aromatic ring with an iodide ion. The product is then purified to remove unreacted 3,5-diiodotyrosine and the metal chelate. 3DILT reacts with antibodies in a luminescence immunoassay to produce light that can be detected. The detection limit of this assay is 10 pg/mL.Fórmula:C9H9I2NO3Pureza:Min. 95%Peso molecular:432.98 g/mol3-(4-Hydroxyphenyl)hex-4-ynoic acid
CAS:Versatile small molecule scaffoldFórmula:C12H12O3Pureza:Min. 95%Peso molecular:204.22 g/mol3-Boc-3-azabicyclo[3.2.1]octan-8-amine
CAS:Versatile small molecule scaffoldFórmula:C12H22N2O2Pureza:Min. 95%Peso molecular:226.32 g/molc3-Ethylbenzoic acid
CAS:C3-Ethylbenzoic acid is an organic compound that can be synthesized from the reactants ethyl bromide, propylene oxide, and acetic anhydride. The synthesis of C3-Ethylbenzoic acid is a stepwise process in which the starting materials are converted to intermediates and then reacted to form the desired product. The reaction mechanism involves bond cleavage, which generates a carboxylic acid group on one end of the molecule and a phenyl group on the other end. C3-Ethylbenzoic acid interacts with clausamine and isoprene during transport through cell membranes. This interaction may lead to increased permeability of cell membranes by c3-ethylbenzoic acid.Fórmula:C9H10O2Pureza:Min. 95%Peso molecular:150.17 g/molEthyl 4-bromoacetoacetate
CAS:Ethyl 4-bromoacetoacetate is a chemical compound that is used in the synthesis of quinoline derivatives. It also has antiinflammatory properties and can be used to treat inflammatory diseases such as arthritis. The thermal expansion of this compound is greater than that of water, which can be useful in treating respiratory problems by providing increased oxygen transport. Ethyl 4-bromoacetoacetate is a reactive chemical that reacts with hydrochloric acid to produce hydrogen gas and ethyl bromide gas. It also undergoes nucleophilic substitutions at the carbon atom adjacent to the acetoacetate group. This reaction solution can be analyzed using magnetic resonance spectroscopy, which produces data on the sequences of this compound's atoms and its antiinflammatory activity.Fórmula:C6H9BrO3Pureza:90%NmrPeso molecular:209.04 g/mol4-Formylbenzoic acid
CAS:4-Formylbenzoic acid is an organic compound with the molecular formula CH2=C(O)CH=CHCO2H. It is a white solid that is soluble in water and has a strong, unpleasant odor. 4-Formylbenzoic acid has been shown to have affinity for binding to odorous molecules such as sulfur compounds, amines, and mercaptans. The binding of these molecules to the 4-formylbenzoic acid leads to a decrease in their odor concentration. This process can be done using electrochemical impedance spectroscopy or optical sensors. The oxidation of 4-formylbenzoic acid by trifluoroacetic acid produces 2-formylphenol and formaldehyde, which are themselves volatile compounds with an unpleasant odor. These reactions may be used as wastewater treatment methods. Langmuir adsorption isotherm may be used as an analytical method for measuring the concentration of 4-formylbenzoic acid
Fórmula:C8H6O3Pureza:Min. 98 Area-%Forma y color:White Yellow PowderPeso molecular:150.13 g/mol2,4,6-trichloropyridine-3-carbonitrile
CAS:Versatile small molecule scaffoldFórmula:C6HCl3N2Pureza:Min. 95%Peso molecular:207.4 g/molFmoc-D-Ala-OH
CAS:Fmoc-D-Ala-OH is a synthetic cyclic peptide that has been shown to have anticancer properties. This compound was synthesized by solid-phase chemistry and exhibits an inhibitory effect on cancer cells. Fmoc-D-Ala-OH blocks the synthesis of proteins in cancer cells, leading to cell death. It also inhibits the activity of serine proteases such as degarelix acetate, which are important for cancer cell growth and metastasis.Fórmula:C18H17NO4Pureza:Min. 95%Forma y color:PowderPeso molecular:311.33 g/mol7H,8H-Pyrido[2,3-d]pyridazin-8-one
CAS:Versatile small molecule scaffoldFórmula:C7H5N3OPureza:Min. 95%Forma y color:PowderPeso molecular:147.13 g/molFmoc-N-methylglycine
CAS:Fmoc-N-methylglycine is a modified form of the amino acid glycine, which has been modified to include a reactive group that can be used to link other molecules. This molecule has gram-negative bacterial activity and exhibits potent antibacterial activity against many gram-positive bacteria. Fmoc-N-methylglycine is also an antimicrobial peptide with binding constants in the nanomolar range. It is also an agent that binds to serotonin, which may explain its effects on mood and sleep. Fmoc-N-methylglycine can be synthesized using stepwise solid phase synthesis methods or by conjugation with other molecules.Fórmula:C18H17NO4Pureza:Min. 95%Peso molecular:311.33 g/mol
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