Building Blocks

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

1-[(tert-Butyldimethylsilyl)oxy]cyclopropane-1-carbaldehyde is a cyclopropanecarboxylic acid that can be prepared by reacting cyclopropane with an ester of ethoxyethyl chloride. It has been used as a precursor for the synthesis of sulfoxide and sulfone derivatives. Cyclopropanecarboxylic acids are used in the preparation of chlorides, esters, and solvents. This compound has also been used as a reagent for the synthesis of oxalyl chloride and pyridinium chloride. 1-[(tert-Butyldimethylsilyl)oxy]cyclopropane-1-carbaldehyde can be purified by recrystallization from organic solvents such as benzene or ether, or it can be purified by preparative thin layer chromatography (PTLC).

<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-Methoxy-5-methylbenzaldehyde is a natural product that has been identified as an intermediate in the biosynthesis of the sesquiterpene, ursolic acid. It can be synthesized by reacting piperazine with methoxymethyl chloride. 3-Methoxy-5-methylbenzaldehyde has also been used for labeling proteins and nucleic acids. The technique of chromatographic mass spectrometric detection uses this compound to detect volatile compounds in headspace by gas chromatography.</p>

2-Propylcyclohexanol is a cyclic alcohol that is used as a solvent in organic chemistry. It has two different forms: cis-2-proptyclohexanol and trans-2-proptyclohexanol, which is a mixture of the two. 2-Propylcyclohexanol can be used as a bifunctional reagent for bond cleavage reactions and dehydration reactions. This compound also has properties that make it useful as an organic solvent, such as its ability to dissolve hydronium ions and its relatively low boiling point. 2-Propylcyclohexanol can be used in microscopy because it does not interfere with fluorescence detection or other light sources. It can also be used in the preparation of carbohydrates. The monomers from which this compound is made are cyclic, meaning that they are shaped like circles or rings. These monomers are made up of carbon atoms, hydrogen atoms, and oxygen atoms.

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>N-[(Allyloxy)carbonyl]glycine is a synthetic compound that is used as a pharmaceutical agent. It is one of the four stereoisomers of N-allyloxycarbonylglycine, which are all synthesized by solid-phase synthesis. This drug was shown to inhibit the growth of cancer cells and may be useful in treating animals infected with infectious diseases. The antimicrobial activity of N-[(Allyloxy)carbonyl]glycine has been demonstrated using bacterial cultures, which showed that it inhibits the growth of bacteria by inhibiting protein synthesis. It also has been shown to have an effect on cellular processes such as DNA replication and transcription.</p>

<p>Prop-2-en-1-yl 2-iodoacetate is a reactive, hydroxyl group containing organometallic molecule that is used as a polymerization initiator in organic reactions. Prop-2-en-1-yl 2-iodoacetate is also used as an agent for catalytic reduction of hydrocarbons and as a reagent in the synthesis of organic compounds. This compound can also be used to synthesize polymers with hydrophobic effect by reacting with halides. The mechanism of this reaction involves formation of a carbocation intermediate followed by nucleophilic attack on the propargyl cation.</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>

Versatile small molecule scaffold

<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>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>