Building Blocks

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about 4-(Dibromomethyl)-2(1H)-quinolinone including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about N-(5-bromo-4-chloro-1H-indol-3-yl)pyrazine-2-carboxamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 4-[(1,1-Dimethylethoxy)carbonyl]-2-thiomorpholineacetic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 2,6-Di-tert-butyl-4-(morpholinomethyl)phenol 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>Please enquire for more information about 1,1-Dimethylethyl 4-[3-[[4-[[[2-[(2S)-2-cyano-4,4-difluoro-1-pyrrolidinyl]-2-oxoethyl]amino]carbonyl]-6-quinolinyl]methylamino]propy l]-1-piperazinecarboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 6-(Trifluoromethyl)-1,4-oxazepane hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,6-Dimethoxy-4-hydroxybenzylamine is a fine chemical that is used as a versatile building block for the synthesis of complex compounds. It is also used as a reagent and reaction component in various chemical reactions. CAS No. 130632-98-3.</p>

<p>Please enquire for more information about 2-(2,6-Dimethylpyridin-3-yl)propan-2-amine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,3-Epoxy-1-(1-ethoxyethoxy)propane is a water-insoluble solid that has been shown to form stable complexes with metal ions. It is soluble in hydrochloric acid and is polymerized by cationic polymerization. 2,3-Epoxy-1-(1-ethoxyethoxy)propane reacts with the hydroxyl group of polymers to produce epoxides. The epoxide ring can be opened to produce ethers or oxiranes through ring opening reactions. 2,3-Epoxy-1-(1-ethoxyethoxy)propane is an acidic compound and reacts with water vapor to form hydroxy groups. This compound can also be synthesized by transfer reactions from 1,2,4,5-tetrahydrobenzene and ethylene oxide.</p>

<p>Givinostat hydrochloride is a research chemical that has shown potential in various fields. It is a molybdenum-based compound that has been studied for its effects on dopamine release and hydrogen evolution. Givinostat hydrochloride has also been investigated as an osteoclast inhibitor, which may be beneficial in the treatment of bone-related disorders such as osteoporosis. Additionally, it has shown promise as a retinoid and calpain inhibitor, suggesting its potential use in dermatological conditions and neurodegenerative diseases. The compound contains fluorine atoms, making it suitable for imaging studies using fluorine MRI techniques. Givinostat hydrochloride has been tested on MDA-MB-231 cells and has shown inhibitory effects on their growth, indicating its potential as an anticancer agent.</p>

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about 1H-Pyrrole-2,3,4,5-tetracarboxylic acid 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>Debacarb is a subtilis mutant strain that produces the active substances debacarb and debacin. Debacarb inhibits the mitochondrial cytochrome b-245, which is an enzyme in the electron transport chain of mitochondria. It also inhibits bacterial growth by binding to nicotinic acetylcholine, which is an enzyme involved in the synthesis of bacterial cell walls. The target enzymes for this compound are not yet known. The bacterium Agrobacterium tumefaciens was found to be sensitive to Debacarb, but resistant strains were also obtained. Debacarb has been used as an agrochemical against bacterial strains such as Pseudomonas syringae and Erwinia carotovora. The effective dose for Debacarb varies depending on the bacterial strain. The most common effective doses are between 2 and 5 ppm, but higher concentrations may be needed against some bacteria.br&gt; Debacarb can inhibit polymerase chain reactions, which</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>