Building Blocks

<p>Versatile small molecule scaffold</p>

<p>Methyl 3-methanesulfonamidobenzoate is an organic compound that is used as a reagent in organic synthesis. It has the chemical formula CH3O2C(CH2)2SO2CH=NOH. Methyl 3-methanesulfonamidobenzoate is a methyl ester of benzoic acid, which is also known as methyl benzoate. This compound has been shown to react with DNA, forming adducts with guanine and cytosine bases.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-Methyl-2-(propan-2-yl)butanoic acid is an inhibitor of cancer, which is structurally related to sulfamic acid. It has been shown to inhibit the growth of bacteria by binding to metal hydroxides and acting as a free radical scavenger. 3-Methyl-2-(propan-2-yl)butanoic acid inhibits the protease activity of trypsin and aminopeptidase and has depressant effects on the central nervous system. This compound also inhibits serotonin reuptake in the rat brain, suggesting that it may be a potential antidepressant. 3-Methyl-2-(propan-2-yl)butanoic acid has been shown to inhibit HIV infection by blocking the activation of tnf alpha.</p>

<p>Ethyl (Benzyloxy)acetate is a β-unsaturated ketone that is used in the synthesis of peroxisome proliferators. It is also used in the asymmetric synthesis of β-unsaturated ketones. Ethyl (Benzyloxy)acetate has been shown to induce inflammation and inhibit serine protease, which may be due to its ability to bind to hydroxyl groups and heterocycles. It can also act as an anti-HIV agent by binding to the hydroxyl group of insulin, which causes insulin resistance. This compound is also used as a solvent for organic chemistry reactions, including the conversion of ethyl formate into acetic acid.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>N-Hydroxy-4-phenylbutanamide is a toolbox hydroxamic acid that has been shown to activate by reacting with the carbonyl group of an arylesterase. This reaction will generate an aldehyde, which can then undergo cyclodehydration in the presence of sodium periodate to form an alkene. The chiral nature of this molecule allows for selective activation on either the left or right side of the molecule. The aerobic conditions are required for this reaction to take place and it can be performed at room temperature. N-Hydroxy-4-phenylbutanamide is also used as a reagent in organic synthesis, crystallography, and alkene synthesis.</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-Amino-N-ethylbenzamide is a synthetic compound that is used in the synthesis of quinazolinones and other pharmaceuticals. It is also used as a reagent for selective halogenation. 2-Amino-N-ethylbenzamide can be synthesized from anthranilic acid, which is produced by the degradation of amino acids in the body, and chloroform. The chlorination of this compound yields 2-chloroamino-N-ethylbenzamide. This reaction can be done in two ways: regioselectively or regiocontrolled. Regioselective reactions are those that have a specific orientation on the benzene ring, while regiocontrolled reactions are less specific.<br>2-Amino-N-ethylbenzamide has been used to produce trifluoromethylated compounds, which are often found in pharmaceuticals such as fluoroquinol</p>