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>Benzaldehyde, 2-amino-5-nitro-, is a reagent that can be used in organic synthesis as an optical and functionalized nitro compound. It has been used to synthesize chiral nitriles and has been used in the synthesis of some ligands. This compound contains two nitro groups and one cyano group, which are both activated for nucleophilic substitution reactions. Benzaldehyde, 2-amino-5-nitro-, also has a phenylhydrazone functionality that can be converted into azo compounds. This reagent is an analogue of benzaldehyde with the addition of two nitro groups.</p>

<p>(3-Methylthiophen-2-yl)(phenyl)methanone is an organic compound that belongs to the class of substituted thiophenes. This compound has been synthesized by thermally or photochemically induced cycloaddition of 2-benzoylthiophene and methyl acetylene. The compound has a triplet emission with a maximum at 637 nm. It also reacts with isobutylene in the presence of ultraviolet light to form a carbonyl group. This reaction is used for the detection of isobutylene in air, as it produces a strong absorption band at 515 nm.</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>Rhosin hydrochloride is a cardiac glycoside derived from the plant Rhosinus peregrinus. It has been shown to have a regulatory effect on cardiac hypertrophy, and has been used in animal experiments to treat cancer. Rhosin hydrochloride is also known to inhibit cell factor and regulatory adhesions, which are proteins that aid in the binding of cells to other cells or tissue. It has been shown to be effective at inhibiting the uptake of calcium ions by rat cardiomyocytes. These properties make rhosin hydrochloride an attractive target for future research into cardiovascular disease treatment.</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>Dec-9-en-1-amine is a heterobifunctional amine with a diazonium salt. It can be used to immobilize biomolecules to surfaces using electrochemical methods. Dec-9-en-1-amine reacts with oxalyl chloride to produce the corresponding amide, which is then reacted with a secondary amine to form an oxazoline. The reaction of a primary amine with the oxazoline forms an azide and the final product is an oxazolidinone. The hybridization of DNA fragments can be detected by labeling one of the strands with a fluorescent dye and measuring changes in fluorescence as the two strands separate during hybridization.</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>6-Phenoxynicotinic acid is an anticancer agent that is potent against a number of human cancer cell lines. It has shown anti-cancer efficacy in animal models and is known to interact with the cancer cells by modifying their DNA. 6-Phenoxynicotinic acid inhibits the growth of cancer cells by inhibiting the synthesis of specific proteins required for cell division. This compound has been synthesized and shown to have potent anticancer activity, which may be due to its ability to inhibit tyrosine kinases, leading to inhibition of protein synthesis.</p>

<p>3-(Pyridin-2-yloxy)benzoic acid is an organic compound that belongs to the group of anilides. It has been shown to be toxic to plants by inhibiting their chlorophyll production and by causing phytotoxicity. 3-(Pyridin-2-yloxy)benzoic acid also inhibits the germination of seeds, primarily due to its inhibition of growth hormone activity. 3-(Pyridin-2-yloxy)benzoic acid can be used as a herbicide because it is highly effective against broadleaf plants, but not grasses. This compound is also relatively non-toxic to mammals and birds, but can cause skin irritation in humans.</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-(2,2-Dimethylpropyl)benzoic acid is an organic compound with the formula CH3COCH2C6H5CO2H. It is a white crystalline solid that is soluble in water and polar organic solvents. The compound is used in the synthesis of other compounds. 2-(2,2-Dimethylpropyl)benzoic acid can be prepared by reacting benzoic acid with magnesium to form a Grignard reagent, which reacts with chlorobenzene to yield the desired product. This compound has been shown to react selectively with substituents on benzyl chloride to produce substituted benzoates.</p>

<p>5-(Bromomethyl)-1,3-oxazolidin-2-one is a synthetic compound that has been shown to be pharmacologically active in mice. It can be synthesized by the electrochemical oxidation of benzene and alcohols. 5-(Bromomethyl)-1,3-oxazolidin-2-one has been shown to have selectivities for cyclic and nucleophilic substrates over tetrafluoroborate substrates. The yields of this reaction are typically low due to the competing reactions between the substrate and oxidant. 5-(Bromomethyl)-1,3-oxazolidin-2-one has been shown to have selective chiral centers due to its spirocyclic structure. It also shows pharmacological effects in mice, which may be due to its ability to inhibit cyclooxygenase (COX) activity.</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>N-Butyl-1H-1,3-benzodiazol-2-amine is an organic compound that belongs to the group of benzimidazoles. It is a fungicide that inhibits the growth of fungi by inhibiting their DNA synthesis. This drug has been shown to inhibit the growth of fungi that cause plant diseases such as rice blast, wheat stem rust and barley yellow dwarf.</p>

<p>Versatile small molecule scaffold</p>

<p>4-Cyano-4-phenylpiperidine hydrochloride is used as an intermediate in the synthesis of organic compounds. It is a white crystalline solid that reacts with water to form hydrogen cyanide and 4-phenylpiperidine. This compound has been shown to be a potent inhibitor of thionyl chloride and benzyl chloride, which are both toxic industrial chemicals. 4-Cyano-4-phenylpiperidine hydrochloride also reacts with diethanolamine to form a benzyl ether, which can then react with other nucleophiles such as piperidine to produce amines.</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>Methyl 2-(2-acetyl-3-hydroxyphenyl)acetate (1) is an ester that can be synthesized by reacting methanol with isobenzofuran. The radical cations of 1 are stable, and the spectra show a strong C=O stretching frequency at 1750 cm−1, as well as a weak C=C stretching frequency at 1360 cm−1. These spectral data were confirmed by infrared and mass spectrometry. The synthesis of 1 was also confirmed by the analysis of its electron impact mass spectrum, which shows molecular ion peaks at m/z 107 and 131.<br>Methyl 2-(2-acetyl-3-hydroxyphenyl)acetate has been isolated from Australian rainforest plants.</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-(1-Chloroethyl)-1,3,5-trimethylbenzene is a solvents that can be used to make cationic polymers. It is a compound that has been shown to be an effective inhibitor of cationic polymerization with styrene. 2-(1-Chloroethyl)-1,3,5-trimethylbenzene can also be used as an initiator in the synthesis of ethylene dichloride. This chemical is insoluble in water and is not reactive with acids or alkalines.</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>Ethyl (4-formylphenoxy)acetate is a molecule that belongs to the group of quinoline derivatives. It is a copper complex that has shown cytotoxic activity against cancer cells in vitro. The cytotoxicity of ethyl (4-formylphenoxy)acetate has been attributed to its ability to form conjugates with monoclonal antibodies, which may be important for treatment and diagnosis of cancer. Studies have demonstrated the interaction between ethyl (4-formylphenoxy)acetate and DNA, as well as the application of radiation and crystallography techniques to optimize labeling.</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>