Building Blocks

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

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>

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>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

N-Phenyl-2-(dicyclohexylphosphino)pyrrole is a palladium catalyst used in organic synthesis. It is soluble in anhydrous solvents and is selective for reactions that require chloride as the source of the leaving group, such as cyanoacetic acid and phenylbutyrate. N-Phenyl-2-(dicyclohexylphosphino)pyrrole can be prepared by reacting bromobenzene with dimethyl acetylenedicarboxylate followed by treatment with ammonium chloride and heating at reflux. The reaction product can be isolated by precipitation from a mixture of ethanol and water.

<p>5-(4-Fluorophenoxy)pyridin-2-amine is a chemical compound which is used in the preparation of Chinese medicines. It has been shown to interact with calcium carbonate, section and calibration, as well as radiation and particle. 5-(4-Fluorophenoxy)pyridin-2-amine also has significant interactions with ethanolic extracts and servicing. This compound is found in dynamometers and optical systems, and can be used for positioning purposes. 5-(4-Fluorophenoxy)pyridin-2-amine can be used to dry weight and calibrate an optical system. It also has optically detectable properties that are useful for laser ablation preparations.</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

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>

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>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>1-Benzylpyridin-4(1H)-one is an organic compound that belongs to the group of benzyl compounds. It is a colorless oil with a sweet, floral odor. 1-Benzylpyridin-4(1H)-one is used as an intermediate in organic chemistry and reacts with alkenes, sulfoxides, and sulfides to form intermediates. It also reacts with alkynes to form triflic acid esters. The hydrolysis of this compound produces pyridine and benzaldehyde. This compound has been used in the synthesis of sulfoxide antibiotics such as cefotaxime and ceftazidime.</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Benzyloxy(methylidene)amine (BAM) is a selective and stereoselective mediator for the asymmetric synthesis of guanine. It is an amine that has been shown to cause carcinogenesis in rats. In addition, BAM is reactive and can be used at nanomolar concentrations in reactions to monitor the progress of the reaction. This mediator can form a radical coupling with piperidine, which produces a ferrocenyl-substituted guanosine.</p>

2-Chloro-6-methoxyphenol is an organic compound that is used as a sample pretreatment agent. It is used in the preparation of fatty acids, which are important in the production of polymers and other materials. The reactivity of this compound can be described by a reaction mechanism involving hydroxy groups, which allows it to react with water to form 2,4-dichlorophenol and hydrochloric acid. 2-Chloro-6-methoxyphenol has been shown to inhibit the growth of many bacterial strains, including those found in wastewater. This product is also nontoxic and nonflammable. It does not contain any toxic impurities or volatile organic compounds (VOCs).

<p>2,4-Dichloro-6,7-dimethoxyquinoline is a quinoline compound that has been used to investigate the enzyme methyltransferase. This chemical was found to bind to the quinoline site of the enzyme and had a high homology with other inhibitors of this type. 2,4-Dichloro-6,7-dimethoxyquinoline also showed potency against a number of methyltransferases and inhibited methylation reactions in vitro. The thermodynamic parameters for binding were determined using isothermal titration calorimetry.</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

Versatile small molecule scaffold

<p>4-(Hydroxymethyl)-7-methoxy-2H-chromen-2-one is a fluorescing compound with an ultraviolet absorption maximum of 330 nm and a visible absorption maximum at 420 nm. It has been shown to be soluble in methanol, chloroform, acetone, ether, and benzene. The molecule has a molecular weight of 188.4 g/mol and an esters composition of 2% fatty acid esters. It also absorbs light at 220 nm and emits light at 350 nm. 4-(Hydroxymethyl)-7-methoxy-2H-chromen-2-one has been shown to be very sensitive to the presence of fatty acids in the environment.</p>

<p>2-Benzylcyclohexan-1-amine is an oxime, which is a class of organic compounds that are derived from an amine and are characterized by the presence of at least one nitrogen atom in their structures. It can be synthesized by deuteration of cyclohexanone with deuterium gas. The reaction mechanism for this process includes catalytic reduction, acetylation, pyrolytic elimination, and reductive amination. 2-Benzylcyclohexan-1-amine has been shown to have a spectrum similar to the postulated spectrum for the compound N-methylphenethylamine, which has been proposed as a possible neurotransmitter in humans.</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

1-Methyl-5-oxopyrrolidine-2-carboxylic acid is a pyroglutamate derivative that is synthesized by the reaction of methyllithium with a ketone. It is used as a reagent for the synthesis of esters and organolithium compounds. Racemization occurs when this compound reacts with an alcohol or phenol to form an ester or ether, respectively. The Grignard reagents are not reactive in the presence of air, but react readily in the presence of water or alcohol. Methyllithium (MeLi) and aryllithium (ArLi) are both organolithium reagents that react with alkyl halides to form organometallic compounds.

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>4,6-Dimethyl-2-(methylsulfanyl)pyridine-3-carbonitrile is a pyridine derivative that is prepared by the reaction of 4,6-dimethylpyridine with aluminum hydride. The compound has the azomethine moiety in its structure and can be used as a starting material for the synthesis of other compounds.</p>

<p>1-(4-Bromobenzyl)-1H-imidazole is a compound that binds to the active site of enzymes and inhibits their activity. It is used as a research tool in molecular modeling, pharmacokinetics, and cancer chemotherapy. 1-(4-Bromobenzyl)-1H-imidazole has been shown to inhibit the growth of prostate cancer cells by inhibiting testosterone levels and also to be effective against leukemia cells. The drug has been shown to be a potent inhibitor of recombinant human catalysis with an IC50 value of 1 nM. This inhibition may be due to its ability to form a triazolium ring, which inhibits the enzymatic activity of catechol oxidase.</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>