Building Blocks
Sottocategorie di "Building Blocks"
- Acidi boronici e derivati dell'acido boronico(5.778 prodotti)
- Building Blocks Chirali(1.243 prodotti)
- Building Blocks Idrocarburici(6.098 prodotti)
- Building Blocks organici(61.036 prodotti)
Trovati 205240 prodotti di "Building Blocks"
tert-Butyl N-(6-bromo-1-benzothiophen-2-yl)carbamate
CAS:Versatile small molecule scaffold
Formula:C13H14BrNO2SPurezza:Min. 95%Peso molecolare:328.23 g/mol4-Chloro-2,5,6-trimethylpyrimidine
CAS:Versatile small molecule scaffold
Formula:C7H9ClN2Purezza:Min. 95%Peso molecolare:156.61 g/mol1-Amino-3-(1,3-dioxaindan-5-yloxy)propan-2-ol
CAS:Versatile small molecule scaffold
Formula:C10H13NO4Purezza:Min. 95%Peso molecolare:211.21 g/mol8-Phenyl-1-oxa-3-azaspiro[4.5]dec-2-en-2-amine
CAS:Versatile small molecule scaffoldFormula:C14H18N2OPurezza:Min. 95%Peso molecolare:230.31 g/mol2,2,2-Trifluoro-1-(piperidin-2-yl)ethan-1-ol
CAS:Versatile small molecule scaffoldFormula:C7H12F3NOPurezza:Min. 95%Peso molecolare:183.17 g/mol3-Bromo-5H,6H,8H-[1,2,4]triazolo[3,4-c][1,4]oxazine
CAS:Versatile small molecule scaffoldFormula:C5H6BrN3OPurezza:Min. 95%Peso molecolare:204.02 g/mol2-Amino-3-Bromo-6-trifluoromethylpyridine
CAS:Versatile small molecule scaffoldFormula:C6H4BrF3N2Purezza:Min. 95%Peso molecolare:241.01 g/molMethyl 2-hydroxy-4-methylvalerate
CAS:Methyl 2-hydroxy-4-methylvalerate is an organic compound that belongs to the class of fatty acids. It is a colorless liquid with a fruity odor. Methyl 2-hydroxy-4-methylvalerate has been shown to inhibit the formation of reactive oxygen species and has antioxidant potential. It also inhibits bone resorption, which may be due to its ability to reduce levels of isobutyric acid in rats and humans. Methyl 2-hydroxy-4-methylvalerate has been found in tropical fruits such as mangoes, durians, and papayas.
Formula:C7H14O3Purezza:Min. 95%Peso molecolare:146.18 g/mol3-(3-Fluorophenoxymethyl)-5H,6H,7H,8H,9H-[1,2,4]triazolo[4,3-a]azepine
CAS:Versatile small molecule scaffoldFormula:C14H16FN3OPurezza:Min. 95%Peso molecolare:261.29 g/mol6-Methoxy-1,2-benzoxazol-3-amine
CAS:Versatile small molecule scaffold
Formula:C8H8N2O2Purezza:Min. 95%Peso molecolare:164.16 g/mol2-(2-Chlorophenyl)-1-phenylethan-1-one
CAS:Versatile small molecule scaffold
Formula:C14H11ClOPurezza:Min. 95%Peso molecolare:230.69 g/molEthyl 4-(4-chloro-3-nitrobenzenesulfonamido)benzoate
CAS:Versatile small molecule scaffoldFormula:C15H13ClN2O6SPurezza:Min. 95%Peso molecolare:384.8 g/mol(4-Methyl-1H-indol-2-yl)methanol
CAS:Versatile small molecule scaffold
Formula:C10H11NOPurezza:Min. 95%Peso molecolare:161.2 g/mol5-(Dimethylamino)-2-fluorobenzoic acid
CAS:Versatile small molecule scaffold
Formula:C9H10FNO2Purezza:Min. 95%Peso molecolare:183.18 g/mol(2S,4R)-1-Boc-2-Hydroxymethyl-4-aminopyrrolidinehydrochloride
CAS:Versatile small molecule scaffold
Formula:C10H21ClN2O3Purezza:Min. 95%Peso molecolare:252.74 g/molN-(3-Methoxyphenyl)prop-2-enamide
CAS:Versatile small molecule scaffold
Formula:C10H11NO2Purezza:Min. 95%Peso molecolare:177.2 g/mol2-Chloro-3,4-dihydronaphthalen-1(2H)-one
CAS:2-Chloro-3,4-dihydronaphthalen-1(2H)-one is a sulfoxide with significant antifungal activity. It has been shown to be effective against Candida albicans and other fungi, including Aspergillus niger and Mucor racemosus. It is commonly used as an electrolyte in electroluminescent devices, such as light emitting diodes (LEDs). The reaction time for the formation of 2-chloro-3,4-dihydronaphthalen-1(2H)-one from potassium sulfate is dependent on the acid catalyst used. Organic chemists have shown that the use of 2-chloro-3,4-dihydronaphthalen-1(2H)-one can inhibit leukotriene synthesis.
Formula:C10H9OClPurezza:Min. 95%Peso molecolare:180.63 g/mol4-(2-Amino-4-methylpentanoyl)piperazin-2-one
CAS:Versatile small molecule scaffold
Formula:C10H19N3O2Purezza:Min. 95%Peso molecolare:213.28 g/mol1-(Butane-1-sulfonyl)piperidine-2-carboxylic acid
CAS:Versatile small molecule scaffoldFormula:C10H19NO4SPurezza:Min. 95%Peso molecolare:249.33 g/mol4-(chloromethyl)-1-methyl-1H-imidazole hydrochloride
CAS:Prodotto controllatoVersatile small molecule scaffold
Formula:C5H8Cl2N2Purezza:Min. 95%Peso molecolare:167.03 g/mol(2-Chloroethoxy)(2-chloroethyl)phosphinic acid
CAS:Versatile small molecule scaffold
Formula:C4H8Cl2O3PPurezza:Min. 95%Peso molecolare:205.98 g/mol2-Methyl-3-oxo-pentanoicacid methyl ester
CAS:The synthesis of 2-methyl-3-oxo-pentanoic acid methyl ester is accomplished by a three step process. The first step is the intramolecular condensation of 2,2-dimethylpropionic acid with acetone to form a 1:1 mixture of 3,4-dihydroxybutyl and 4,4-dihydroxybutyl esters. The second step is the selective transesterification of the 3,4-dihydroxybutyl ester with benzaldehyde. This reaction provides an optically pure 2-methyl-3-oxo-pentanoic acid methyl ester as the major product. The third step is an aldol condensation between the ketone from the second step and acetone to produce another optically pure 2,2 dimethylpropionic acid methyl ester.Formula:C7H12O3Purezza:Min. 95%Peso molecolare:144.17 g/mol1-(2-Isothiocyanatoethyl)-4-methoxybenzene
CAS:Versatile small molecule scaffold
Formula:C10H11NOSPurezza:Min. 95%Peso molecolare:193.27 g/molN-(3-Hydroxyphenyl)-2-(2-oxopyrrolidin-1-yl)acetamide
CAS:Prodotto controllatoN-(3-Hydroxyphenyl)-2-(2-oxopyrrolidin-1-yl)acetamide is a research tool that is used as an activator or ligand to study the function of receptors, ion channels and other proteins. It binds to cell surface receptors and activates them by mimicking the endogenous ligands. This compound has been shown to be a high purity reagent with protein interactions.Formula:C12H14N2O3Purezza:Min. 95%Peso molecolare:234.25 g/mol3-(3-Fluorophenyl)butanoic acid
CAS:Versatile small molecule scaffold
Formula:C10H11FO2Purezza:Min. 95%Peso molecolare:182.19 g/mol2-Methyl-3-[2-(morpholin-4-yl)ethoxy]phenol
CAS:Versatile small molecule scaffold
Formula:C13H19NO3Purezza:Min. 95%Peso molecolare:237.29 g/molDiisopropylphosphine, 10wt.% in hexane
CAS:Please enquire for more information about Diisopropylphosphine, 10wt.% in hexane including the price, delivery time and more detailed product information at the technical inquiry form on this page
Formula:C6H15PPurezza:Min. 95%Peso molecolare:118.16 g/mol6-Methyl-3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazine
CAS:Versatile small molecule scaffold
Formula:C8H10N2OPurezza:Min. 95%Peso molecolare:150.18 g/mol2-Phenylbutan-1-amine HCl
CAS:Versatile small molecule scaffold
Formula:C10H15N·HClPurezza:Min. 95%Peso molecolare:185.7 g/mol1-(2-Chloroethyl)-3,5-dimethylcyclohexane
CAS:Versatile small molecule scaffold
Formula:C10H19ClPurezza:Min. 95%Peso molecolare:174.71 g/mol6-[3-(3-Chlorophenyl)-1,2,4-oxadiazol-5-yl]-2,3-dihydropyridazin-3-one
CAS:Versatile small molecule scaffold
Formula:C12H7ClN4O2Purezza:Min. 95%Peso molecolare:274.66 g/molEthyl 1-amino-1-cyclobutanecarboxylate monohydrochloride
CAS:Ethyl 1-amino-1-cyclobutanecarboxylate monohydrochloride is a cyclic carbonyl compound that is used as a building block in organic synthesis. It has been used to synthesize a number of natural products, such as piperarborenine and cyclobutanes. This compound can be synthesized by reacting ethyl chloroformate with cyclobutanecarbaldehyde in the presence of an acid or base catalyst. The steric and geometric properties of this molecule are highlighted below.
Formula:C2H5O2CC4H6NH2·HClPurezza:Min. 95%Peso molecolare:179.64 g/mol2-(Chloromethyl)-5,6,7,8-tetrahydroquinazolin-4(3H)-one
CAS:Versatile small molecule scaffold
Formula:C9H11ClN2OPurezza:Min. 95%Peso molecolare:198.65 g/mol5-Aminohexanoic acid hydrochloride
CAS:Versatile small molecule scaffold
Formula:C6H14ClNO2Purezza:Min. 95%Peso molecolare:167.63 g/mol4-(Pyrrolidine-1-sulfonyl)-1H-pyrrole-2-carboxylic acid
CAS:Versatile small molecule scaffoldFormula:C9H12N2O4SPurezza:Min. 95%Peso molecolare:244.27 g/mol3-Hydroxy-5-methylpyridine
CAS:3-Hydroxy-5-methylpyridine (3HMP) is a chemical substance that has been classified as an amine. It is a product of the metabolism of purines, which are nitrogenous bases found in DNA and RNA. 3HMP is produced by aerogenic bacteria (such as Enterobacter), and can be used to estimate the number of these bacteria present in water samples. 3HMP has been shown to have antiviral properties against influenza virus, and can be used as a biomarker for the presence of other viruses in animals. 3HMP also has mineralization properties, which have been studied extensively, particularly with regards to pancreatic disease.
Formula:C6H7NOPurezza:Min. 95%Colore e forma:PowderPeso molecolare:109.13 g/molRef: 3D-FH16174
Prodotto fuori produzione2-Bromo-3,3,3-trifluoro-1-propene
CAS:Prodotto controllato2-Bromo-3,3,3-trifluoro-1-propene is a chemical compound that has been synthesized in an asymmetric reaction. The reactant is bromopropane and the product is 2,2,2-trifluoropropene. The methylene group on the propene molecule is activated by the nucleophilic attack of a fluoride ion from hydrogen fluoride to form a cavity with a highly strained bond. The kinetic study of this reaction revealed that the activation energy for the reaction is 42 kJ/mol. Palladium-catalyzed coupling reactions are catalyzed by palladium and require nonpolar solvents such as toluene or dichloromethane. This type of reaction has been shown to be exothermic with an isolated yield of 1%.
Formula:C3H2BrF3Purezza:Min. 95%Colore e forma:Colorless PowderPeso molecolare:174.95 g/mol4-Chloro-2-hydroxy-6-methylphenylboronic acid
CAS:Versatile small molecule scaffoldFormula:C7H8BClO3Purezza:Min. 95%Peso molecolare:186.4 g/mol4,5-Dihydroxy-2,3-Pentanedione
CAS:4,5-Dihydroxy-2,3-pentanedione is a carbonyl compound that is the product of the oxidation of ascorbic acid. It is used in wastewater treatment and has antimicrobial properties against infectious diseases. This compound has been shown to inhibit protein synthesis by binding to the ribosome and preventing the formation of peptide bonds between amino acids. 4,5-Dihydroxy-2,3-pentanedione has also been shown to bind to plasma proteins, which may be due to its acyl chain structure. 4,5-Dihydroxy-2,3-pentanedione can be synthesized in a catalytic mechanism that involves dehydroascorbic acid and molecular oxygen.
Formula:C5H8O4Purezza:Min. 95%Colore e forma:PowderPeso molecolare:132.11 g/molRef: 3D-FD180770
Prodotto fuori produzionePiperyline
CAS:Piperyline is an alkanoic acid that has shown to be effective against skin cancer. It also has antimicrobial properties, which may be due to its ability to bind metal ions and form polymeric compounds. Piperyline inhibits microbial growth by inhibiting the synthesis of proteins and nucleic acids. The antimicrobial activity is related to its cationic polymerization with hydroxyl groups, which forms a structure that can inhibit microbial enzymes and disrupt microbial cell membranes. This compound also interacts with the skin's natural lipids, making it difficult for microorganisms to attach and grow on the skin. Piperyline is synthesized in organic chemistry laboratories as an amide precursor of other pharmaceuticals such as penicillin.
Formula:C16H17NO3Purezza:Min. 95%Peso molecolare:271.31 g/mol
