Building Blocks

<p>Versatile small molecule scaffold</p>

<p>2-Ethenyl-1-(hydroxylmethyl)cyclopropane is a cyclopropane ring that has been opened by a ring-opening reaction. It is a member of the class of compounds known as olefinic alcohols. These compounds are hydrolyzed to form an ester and an alkene, which can be used in polymerizations. The 2-ethynyl group is a weak hydrogen bond acceptor, meaning that it can react with polar molecules such as water and alcohols. This group also has low energies, which allow for polymerization reactions. This compound is soluble in organic solvents but not in water because of its hydroxyl group, which allows it to form hydrogen bonds with other compounds.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

2-tert-Butyldimethylsilyloxyethanol is a molecule that is used as an antimicrobial agent. It inhibits the efflux pump in gram-negative bacteria, which prevents them from removing antibiotics and other toxic substances from their cells. This results in a high level of antibiotic accumulation within the bacterial cell, which leads to cell death. 2-tert-Butyldimethylsilyloxyethanol has been shown to be effective against Staphylococcus aureus and Escherichia coli (E. coli) but not against Enterobacter aerogenes or Serratia marcescens. 2-tert-Butyldimethylsilyloxyethanol also has antiplasmid activity, inhibiting replication of plasmids in Escherichia coli and Salmonella typhimurium by blocking DNA synthesis at the initiation stage of replication.

<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>2-Azido-1,3-difluorobenzene is a photoactive compound that can be used to form an azide. It has been shown to undergo photochemical reactions to form the triplet state and then isomerize to the singlet state. This reaction can be initiated by a laser beam or other light source, such as sunlight. The triplet state of 2-azido-1,3-difluorobenzene has been shown to react with organic molecules containing electron withdrawing groups on their molecules, such as 2-methoxy-2-methylpropane. When these two substances are mixed together, they react to form an isomerized product that has a carbonyl group in its structure. This reaction could be helpful for developing new synthetic methods for producing pharmaceuticals and other compounds with important functions in chemistry and physics.</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>

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>5-Carboxyoxindole is a synthetic compound that has been shown to be cytotoxic in vitro and in vivo. It has been found to bind to the DNA of cancer cells, preventing DNA synthesis and replication, resulting in cell death. The mechanism of 5-carboxyoxindole is not completely understood but it has been suggested that it inhibits the production of ATP, leading to cell death. Techniques used to synthesize this compound include multistep reactions with yields up to 69%. These reactions are typically carried out at room temperature, although they can also be performed under reflux or microwave conditions.</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>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

1-Amino-1-phenylpropan-2-ol hydrochloride is an enantioselective, chiral amino alcohol that is synthesized by the reaction of aldehydes or ketones with phenylmagnesium bromide. This reaction yields the corresponding amino alcohols in high yields and with excellent enantioselectivity. 1-Amino-1-phenylpropan-2-ol hydrochloride can be used to synthesize various functional groups such as halides, oxazoline, diselenides, sulfonamides and alkenes. It can also be used for catalytic transformations involving other functional groups such as alcohols and alkyl halides.

<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>