Building Blocks

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Pyrimidine-2-carbohydrazide is a bioinorganic compound that has been shown to be active against bacteria, including staphylococcus. It is also effective against tuberculosis and leishmania. Pyrimidine-2-carbohydrazide binds to the bacterial cell membrane and inhibits its growth by preventing the synthesis of essential proteins. This drug's pharmacokinetic properties have been studied using techniques such as bioinorganic and electron paramagnetic resonance spectroscopy. The tetranuclear nature of pyrimidine-2-carbohydrazide makes it an excellent candidate for use with ciprofloxacin in the treatment of leishmaniasis.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2,3-Dihydro-1λ⁶-thiophene-1,1,3-trione is a chemical compound that has been synthesized by the reaction of two molecules of dimethyldioxirane with one molecule of thiol. It is a colorless liquid that can be oxidized to 2,3-dihydro-2λ⁶-thiophene-2,2,4(1H)-trione or reduced to 2-(2'-formylphenyl)ethanol. This chemical is an important precursor for the synthesis of sulfur and nitrogen nucleophiles. The yields are high and it is commercially available.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-Pyrrol-1-ylmethyl-benzoic acid is a silicon-containing compound that can be used as an electropolymerization initiator. It has been shown to be an efficient activator for the polymerization of carbodiimides in the presence of solvents, such as nitro groups and nitro compounds. 4-Pyrrol-1-ylmethyl-benzoic acid is a monomer that can be used in the preparation of biosensors with silicon nitride. This chemical is able to generate pores with diameters ranging from 1 to 10 nm. The permeation of this compound through membranes is also possible.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-Bromomethyl-2-chloroquinoline is an organic compound that contains a pyrrole ring and an alkyl group. It is synthesized by the reaction of 4-bromomethylbenzene with quinoline. This product has been shown to be efficacious against tumor cells in vitro and in vivo, and has antitumor activity. 4-Bromomethyl-2-chloroquinoline is also used as a building block for the synthesis of other heterocyclic compounds. The efficiency of this process depends on the metalation of the pyrrole ring. Lithiation, for example, leads to increased reactivity due to increased electron density on the ring. Alkylation occurs when a reactive alkylating agent reacts with one or more of the bromine atoms on the pyrrole ring, leading to cleavage of carbon bonds in the ring and formation of new bonds between carbon atoms. This reaction</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Dimethyl[(E)-2-(pyridin-2-yl)ethenyl]amine is a substance that belongs to the group of photosensitive polymerization substances. The polymerization reaction starts when it is exposed to light. It has been shown to form a film that can be developed and used as a plate or an emulsion. Dimethyl[(E)-2-(pyridin-2-yl)ethenyl]amine can also be used as an additive in the production of polymeric particles, which are formed by the addition of acrylic acid.</p>

<p>Versatile small molecule scaffold</p>

<p>(S)-3-Bromopropane-1,2-diol is a drug that belongs to the group of leukotriene antagonists. It is an immunogenic agent that inhibits the transport of penicillin-binding proteins in vivo and prevents the synthesis of protein genes. (S)-3-Bromopropane-1,2-diol has been shown to inhibit the growth of Staphylococcus aureus by binding to penicillin-binding protein, which prevents it from synthesizing proteins needed for cell division. This drug has also been found to have antioxidative properties in vitro, which may be due to its ability to scavenge reactive oxygen species.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Bromo-1-(5-methyl-1-phenyl-1H-pyrazol-4-yl)-1-ethanone is a chemical that has been identified as an environmental contaminant. It has been shown to be toxic to aquatic organisms, but not to mammals.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>6,7-Difluoro-1,2-dihydroquinoxalin-2-one is a heterocyclic compound that belongs to the group of substituted quinoxalines. This compound contains two phenolic hydroxyl groups and one hydroxyl group on the benzene ring. 6,7-Difluoro-1,2-dihydroquinoxalin-2-one is obtained by condensation of resorcinol and pyrogallol. It can be synthesized from indoles by reaction with benzene and pyrazine in the presence of a base.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about 1-Bromo-3-methylbicyclo[1.1.1]pentane including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-Acetyl-1-methyl-1H-pyrazole is an oleum that is obtained by nitrating 3,4-dimethylphenol with a mixture of conc. sulfuric acid and fuming nitric acid. It can be used to produce the anhydride of benzene and other aromatic compounds. 3-Acetyl-1-methyl-1H-pyrazole has also been used as a reagent for the preparation of 1,2,4,5,6,7,8,9-octahydroazulene from 1,3,5,7-tetrahydroazulene.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>