Building Blocks
Subcategorías de "Building Blocks"
- Ácidos borónicos y derivados del ácido borónico(5.778 productos)
- Building Blocks quirales(1.243 productos)
- Building Blocks de hidrocarburos(6.098 productos)
- Building Blocks orgánicos(61.042 productos)
Se han encontrado 204339 productos de "Building Blocks"
benzyl(imino)methyl-sulfanone
CAS:Versatile small molecule scaffold
Fórmula:C8H11NOSPureza:Min. 95%Peso molecular:169.24 g/mol5-(4-Methylphenyl)thiophene-2-carbaldehyde
CAS:Versatile small molecule scaffoldFórmula:C12H10OSPureza:Min. 95%Peso molecular:202.27 g/mol5-(4-Bromophenyl)thiophene-2-carbaldehyde
CAS:Versatile small molecule scaffoldFórmula:C11H7BrOSPureza:Min. 95%Peso molecular:267.14 g/mol5-(4-Chlorophenyl)thiophene-2-carbaldehyde
CAS:Versatile small molecule scaffold
Fórmula:C11H7ClOSPureza:Min. 95%Peso molecular:222.69 g/mol5-(3-Bromo-phenyl)-thiophene-2-carbaldehyde
CAS:Versatile small molecule scaffoldFórmula:C11H7BrOSPureza:Min. 95%Peso molecular:267.14 g/mol5-(3-Nitrophenyl)thiophene-2-carbaldehyde
CAS:Versatile small molecule scaffoldFórmula:C11H7NO3SPureza:Min. 95%Peso molecular:233.25 g/mol5-Chloro-1-phenyl-1H-pyrazole-4-carbaldehyde
CAS:Versatile small molecule scaffoldFórmula:C10H7ClN2OPureza:Min. 95%Peso molecular:206.63 g/mol1-Acetamidocyclopropanecarboxylic acid
CAS:Versatile small molecule scaffoldFórmula:C6H9NO3Pureza:Min. 95%Peso molecular:143.14 g/mol3-Chloronaphthalen-2-amine
CAS:3-Chloronaphthalen-2-amine is a high concentration, organic solvent that is soluble in water and stable. It has been shown to be a reductant, which is a substance that donates electrons to another reactant in a chemical reaction. 3-Chloronaphthalen-2-amine can be used as a solvent for underwater applications and may have the ability to reduce nitrogen gas into ammonia. The residue of 3-chloronaphthalen-2-amine can be removed by solvents such as chloroform or ether.
Fórmula:C10H8ClNPureza:Min. 95%Peso molecular:177.63 g/mol5-[(Oxiran-2-yl)methoxy]-1,3-dioxaindane
CAS:Versatile small molecule scaffold
Fórmula:C10H10O4Pureza:Min. 95%Peso molecular:194.18 g/molN-(4-Bromophenyl)-3-oxobutanamide
CAS:N-(4-Bromophenyl)-3-oxobutanamide is a complex molecule that belongs to the class of organocatalysts. It has been shown to show antitubercular activity in vitro, with an MIC of 2.5 µg/mL against Mycobacterium tuberculosis and a MIC of 0.05 µg/mL against Mycobacterium avium complex. It also has been shown to be active as an organocatalyst for the carbonylative synthesis of cyclic carbonate esters from simple alkyl dicarbonates and lithium diisopropylamide, which can be used in organic synthesis. The chemical name for this product is N-(4-bromophenyl)-3-oxobutanamide (NBPBA).Fórmula:C10H10BrNO2Pureza:Min. 95%Peso molecular:256.1 g/molN-(4-Iodophenyl)-3-oxobutanamide
CAS:Versatile small molecule scaffold
Fórmula:C10H10INO2Pureza:Min. 95%Peso molecular:303.1 g/mol5-tert-Butyl-2-methyl-3-furoic acid
CAS:Versatile small molecule scaffold
Fórmula:C10H14O3Pureza:Min. 95%Peso molecular:182.22 g/mol2-(2,3-Dihydro-1H-inden-1-yl)acetic acid
CAS:2-(2,3-Dihydro-1H-inden-1-yl)acetic acid (DHIAA) is an organic compound that belongs to the group of heterocyclic compounds. It is a plant cell growth regulator and has been shown to inhibit inflammatory diseases in animal models. DHIAA has a stepwise mechanism that starts with the formation of an alkoxy radical by hydrogen bond between the hydroxyl group and the double bond. This mechanism leads to the production of a reactive oxygen species, which causes oxidative damage in cells. DHIAA also inhibits fatty acid synthesis, which may be due to its interaction with peroxisome proliferator-activated receptor alpha (PPAR-α).Fórmula:C11H12O2Pureza:Min. 95%Peso molecular:176.21 g/mol2-(2,3-Dihydro-1H-inden-1-yl)ethan-1-ol
CAS:Versatile small molecule scaffoldFórmula:C11H14OPureza:Min. 95%Peso molecular:162.23 g/moltert-Butyl N-(2-phenylethyl)carbamate
CAS:tert-Butyl N-(2-phenylethyl)carbamate is a reagent for the synthesis of amines and amine salts. It is prepared by treating benzonitrile with primary amines in the presence of hydrogen, which mediates the reaction. This tert-butyl carbamate can be isolated in high yield when a solvent such as diethyl ether or tetrahydrofuran is used. The tert-butyl carbamate can be hydrogenated to form an acid chloride, which is then reacted with an alcohol to form an ester. This method has been used in synthesizing many functionalized compounds, including anti-inflammatory drugs. Tert-butyl N-(2-phenylethyl)carbamate also has a conformational effect on solvents, where it causes immiscible solvents to become miscible due to its acidic nature.Fórmula:C13H19NO2Pureza:Min. 95%Peso molecular:221.29 g/mol1-(2-Bromoethyl)-2,3-dihydro-1H-indene
CAS:Versatile small molecule scaffoldFórmula:C11H13BrPureza:Min. 95%Peso molecular:225.12 g/molEthyl 2-(ethylamino)benzoate
CAS:Ethyl 2-(ethylamino)benzoate is an organic compound that is classified as a hydrocarbon. It has a chemical formula of C6H11NO2 and it is colorless and odorless. This substance can be ingested orally or applied topically. Ethyl 2-(ethylamino)benzoate has been shown to have antifungal, antibacterial, antidiabetic, anti-inflammatory, and antipyretic properties. The metal chelate of ethyl 2-(ethylamino)benzoate has been shown to cause cardiotoxicity in rats by inhibiting the synthesis of myocardial contractile proteins. This compound also inhibits the synthesis of collagen, which can lead to inflammatory diseases such as arthritis.
Fórmula:C11H15NO2Pureza:Min. 95%Peso molecular:193.24 g/mol5-(Hydroxymethyl)azepan-2-one
CAS:Versatile small molecule scaffoldFórmula:C7H13NO2Pureza:Min. 95%Peso molecular:143.18 g/molEthyl 2-acetyl-5,5-dimethyl-4-oxohexanoate
CAS:Versatile small molecule scaffoldFórmula:C12H20O4Pureza:Min. 95%Peso molecular:228.28 g/mol
