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>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>3-Phenyl-4-(trifluoromethyl)-1,2-oxazole-5-carboxylic acid is a crystalline compound that is regioselective for the ring opening of epoxides. The compound has been studied in the context of enzymatic reduction and synthesizing epoxide intermediates. It is also a receptor agonist, which may be due to its ability to bind with high affinity to opioid receptors. 3-Phenyl-4-(trifluoromethyl)-1,2-oxazole-5-carboxylic acid has been shown to have toxicological properties in animal studies. This includes an enzyme induction effect and neurotoxicity. 3-Phenyl-4-(trifluoromethyl)-1,2-oxazole-5 carboxylic acid has been optimized for research on stereospecificity.</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>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>2,3,4,5-Tetrahydro-1-benzoxepine-3,5-dione is an intermediate in the synthesis of phenelzine. It is a benzyl derivative that can be synthesized from 2,3,4,5-tetrahydrobenzo[b]thiophene and isopropylmagnesium chloride. This compound has been shown to react with methoxy groups as well as sulfur and alkenyl groups. The reaction with nitro groups leads to the formation of an unstable nitroso compound. The compounds derived from this intermediate have been shown to have significant antibacterial activity against intestinal bacteria such as enterobacteriaceae and coliforms.</p>

<p>Versatile small molecule scaffold</p>

<p>5-Amino-1-methyl-1H-pyrazole-4-carbaldehyde (5AMPC) is a catalyst that activates alkyl groups. It is generated by the reaction of formaldehyde with cyanide. The cyanide group is then replaced by aminomethyl and cyano groups, which can be used in the synthesis of other organic compounds. 5AMPC has been extensively studied for its application as a catalyst in the production of nitriles from carbonyl compounds.</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>Undec-10-en-1-amine is a chemical compound with the molecular formula C11H23N. It has a reactive chemical structure that can undergo reactions with other molecules. Undec-10-en-1-amine is used as a model system in carbohydrate chemistry and biological studies. It is also used in silicon polymerizations, glycopolymer synthesis, and primary amino acid synthesis. Undec-10-en-1-amine has been shown to be cytotoxic, which may be due to its ability to deaminate cytidine residues on DNA. This reaction results in the formation of uracil, which blocks RNA synthesis and leads to cell death.</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-(Piperidin-4-yl)phenol is a potent antipsychotic drug that belongs to the group of piperidines. It has been shown to be active in animal models and as an antipsychotic agent in humans. 4-(Piperidin-4-yl)phenol binds to alpha and beta adrenergic receptors, serotonin receptors, dopamine receptors, and histamine H1 receptors. It has been shown to have high potency and affinity for these receptors. This drug is also cloned from human brain tissue and has acted as a subtype-selective antagonist at cloned human alpha 1A-adrenergic receptor.</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>1-(5-Phenylfuran-2-yl)ethan-1-one is a chemical compound that has been shown to be an effective method for synthesizing indole derivatives from 5-phenyl furan-2-carboxylic acid. The indole ring of the 1-(5-Phenylfuran-2-yl)ethan-1-one is derived from the furan ring, which is formed by a rearrangement of the carboxylic acid. This transformation can also be accomplished with other electrophilic reactants, such as thionyl chloride or phosphorus pentachloride. The synthesis of 1-(5-Phenylfuran-2-yl)ethan-1 can be achieved by the rearrangement of 2,3,4,5 tetrahydrofuran.<br>Synlett 2004, 1670</p>

<p>3-Chloromethyl-4-methyl-furazan is a colorless liquid that is soluble in alcohol, ether and benzene. It has a boiling point of 104°C and an average molecular weight of 183.3. 3-Chloromethyl-4-methyl-furazan reacts with strong bases to form sulfuryl chloride, which is used as a precursor to other compounds. It can also be used for the chlorination of organic compounds or the manufacture of various sulfonyl chlorides.</p>

<p>7-Aminoheptanoic Acid Hydrochloride is a product that is obtained from the reaction of diethyl malonate with hydroxylamine. It is a nucleophilic compound that can react with various electrophiles, such as phthalimide. This product has high yields and can be used in organic synthesis to make other compounds. The crystallization of 7-Aminoheptanoic Acid Hydrochloride can be done by refluxing in hydrochloric acid and then decompressing the solution. The crystallizing agent used for this process can be either an organic solvent or water. This product can also be produced on a large scale using the malonate method.</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>