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>Ethyl 1-benzothiophene-3-carboxylate is a heterocyclic compound that has been shown to be an efficient condensation reagent. This compound has two methylene groups and is used in the synthesis of heterocycles. It can be used as a precursor for the synthesis of amines and pyridopyridazine derivatives, which are often used as reagents in organic chemistry. Ethyl 1-benzothiophene-3-carboxylate can also be used for irradiation experiments. It has been shown that this compound is active at lower temperatures than other benzothiophenes, making it ideal for use in x-ray crystallography experiments.</p>

<p>2-(2-Hydroxyethyl)phenylboronic acid dehydrated is a molecule with a hydroxyl group, a neutral ph, and a hydroxyl group. It is used in the synthesis of nitro compounds and has shown to have an inhibitory effect on protein synthesis. The compound also binds to hyaluronic acid, which may be due to its structural similarity to the sugar glucose.</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>(2R)-2-Hydroxy-1-(2,4,5-trimethoxyphenyl)propan-1-one is an efficient method for the synthesis of adenosine. This method is based on a cyclic reaction with trimethoxybenzene and yields 2 moles of adenosine per mole of trimethoxybenzene. The reaction time is short and the yield is high. This synthetic route has been used to produce large quantities of adenosine for use in pharmacological studies. (2R)-2-Hydroxy-1-(2,4,5-trimethoxyphenyl)propan-1-one can be used as an enantiomer for the synthesis of other compounds. It was also shown that nitrite mediates this reaction</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>[(2-Oxo-2-phenylethyl)sulfanyl]acetic acid is a methyl ester that belongs to the class of alpha,alpha-diphenylacetates. It has been shown to be an effective inhibitor of protein synthesis in bacteria and yeast. This inhibition may be due to its ability to inhibit ribosome function by binding to the 30S subunit of bacterial ribosomes. The acid methyl ester form of [(2-Oxo-2-phenylethyl)sulfanyl]acetic acid is also an inhibitor of protein synthesis in bacteria and yeast, but it does not inhibit ribosome function.</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-[(5-Mercapto-1,3,4-thiadiazol-2-yl)thio]acetic acid (MTTSA) is a fluorescent probe that emits light at a wavelength of 590 nm when irradiated with light. MTTSA has been synthesized using gold nanoclusters as the catalyst. The average diameter of the nanoclusters was determined to be in the range of 2.0 - 3.0 nm, and their average quantum yield was found to be 0.097%. The emission wavelengths can be tuned by varying the size of the nanoclusters. When MTTSA is irradiated with UV radiation, it undergoes photocatalysis and converts organic matter into water and carbon dioxide gas.</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>Tetramethyl-1,3-cyclobutanediol is a diacid that can be used as a monomer for the production of polyesters. It has conformational properties that are different from other diols. Tetramethyl-1,3-cyclobutanediol is soluble in hydrochloric acid and reacts with coatings containing dibutyltin oxide to produce residues. This chemical also reacts with copper oxide, resulting in the formation of copper cyclohexanol and dibutyltin oxide. Tetramethyl-1,3-cyclobutanediol is able to react with carboxylic acids to form esters. This compound has been shown to be employed in the synthesis of polycarboxylic acids such as adipic acid and sebacic acid. Tetramethyl-1,3-cyclobutanediol has been used in the production of polyester resins by reacting with ethylene glycol and tere</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-Chloro-5-methoxybenzene-1-sulfonamide is a selective nematicide that has been shown to be effective against parasitic nematodes. It is a member of the class of compounds known as parasitic nematides. This compound is active against both larval and adult forms of these worms, but it does not affect other organisms or plants. 2-Chloro-5-methoxybenzene-1-sulfonamide is believed to act by binding to specific sites on the nematode's body and interfering with their biological properties.</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>