Building Blocks

<p>Versatile small molecule scaffold</p>

2-(2-Naphthyl)-2-propanol is a reactive chemical that is orally administered, and interacts with tissues to produce extents. The molecule has been shown to be magnetic resonance spectroscopic (MRS) detectable. 2-(2-Naphthyl)-2-propanol reacts with chloride ions and produces 2-chloro-1-naphthol and 2-(2-naphthyl)ethanol, which can be used as biomarkers for its presence in the body. This chemical also reacts with isopropyl groups to form epoxides or peroxides, depending on the extent of reaction. Irradiation of this compound by UV light yields hydroxypyridinium salts. 2-(2-Naphthyl)-2-propanol may interact with metal ions such as iron, copper, or zinc.

8-Methoxychroman-4-one is a natural product that inhibits the activity of dopamine beta-hydroxylase, an enzyme that converts dopamine to norepinephrine. It also has inhibitory effects on dopaminergic neurons in vivo and has been shown to be effective in reversing streptozotocin-induced diabetes in rats. 8-Methoxychroman-4-one may also have potential as a prophylactic agent for diabetic nephropathy. The extract of the rhizomes has been shown to contain both 8-methoxychroman-4-one and oxime, aminoguanidine, which is an inhibitor of nitric oxide synthase.

Versatile small molecule scaffold

<p>7-Chlorobenzo[d]thiazol-2-amine is a synthetic intermediate used in the production of dyes, pigments, and pharmaceuticals. It is prepared by the reaction of 2-aminobenzothiazole with nitrous acid and 7-chloroacetophenone. 7-Chlorobenzo[d]thiazol-2-amine can be cleaved at the 2 position to produce 2,4,5-trichlorobenzothiazole. The infrared absorption spectrum of 7-chlorobenzo[d]thiazol-2-amine has been recorded in the solid phase at room temperature and shows three bands between 1710 cm−1 and 1700 cm−1.</p>

<p>7-Bromo-1,3-benzothiazol-2-amine is a heterocyclic compound with the chemical formula CHBrN. It is synthesized by reacting 2-aminobenzothiazole with aniline in the presence of acid. The product has been shown to have traceless reactions and can be used for solid phase synthesis. 7-Bromo-1,3-benzothiazol-2-amine has been shown to undergo cleavage under acidic conditions, which is useful for the synthesis of other heterocyclic compounds.</p>

<p>Versatile small molecule scaffold</p>

<p>2,2-Dimethyl-1,2,3,4-tetrahydroquinoline is a molecule with the chemical formula C8H10N. It is a white crystalline solid that has a pyridine ring and a tetrahydroquinoline ring. 2,2-Dimethyl-1,2,3,4-tetrahydroquinoline has been shown to interact with nitrogen atoms in its environment. This process can lead to the formation of an N-oxide or carbonyl groups at the nitrogen atom. The molecule has also been shown to react with methyl groups and form stoichiometric amounts of n-oxides or carbonyl groups. 2,2-Dimethyl-1,2,3,4-tetrahydroquinoline can be used as a desorption agent for gas chromatography (GC).</p>

<p>1-Bromo-5-methylnaphthalene is a chemical compound that belongs to the group of organic compounds. It can be synthesized by deoxygenation of 1,2-dibromonaphthalene with lithium diisopropylamide and diisopropylamide in an alkaline medium. The reaction yields high yields of 1-bromo-5-methylnaphthalene. The synthesis can also be achieved by the regioisomeric lithium–diels–alder reaction.</p>

<p>N-(4-Propoxyphenyl)acetamide is a crystalline solid that has the chemical formula C8H11NO2. This compound belongs to the group of hydrogen bond coplanar molecules. It has a molecular weight of 153.19 and a melting point of 209 degrees Celsius. Its crystal structure is monoclinic with chains that are parallel to each other and have an angle of 90 degrees, with four propoxyphenyl groups at one end and one acetamide group at the other end.</p>

<p>Versatile small molecule scaffold</p>

<p>3-(2-Methoxyphenoxy)propanoic acid is a nonracemic compound that is an enantiomer of phenoxyacetic acid. 3-(2-Methoxyphenoxy)propanoic acid has been shown to inhibit the growth of bacteria by inhibiting protein synthesis. It also inhibits the production of proteins essential for cell division and causes bacterial cells to undergo apoptosis, which leads to cell death. 3-(2-Methoxyphenoxy)propanoic acid is active against both Gram-positive and Gram-negative bacteria, but is not active against Mycobacterium tuberculosis or Mycobacterium avium complex.</p>

<p>Versatile small molecule scaffold</p>

<p>5-Azidoquinoline is a molecule with the molecular formula CHN. It is classified as an oxadiazoloquinine and has a range of chemical properties that make it suitable for use in medicine, including its ability to form halides and nitro groups. 5-Azidoquinoline can also be used to synthesize other molecules, such as chloroacetone, by nucleophilic substitution reactions. The electronegativity of the 5-azido group makes it an excellent nucleophile, which allows for kinetic reactions. This molecule has six different heterocycles and can be substituted with halogens or other azides.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>3-(4-Methoxyphenyl)propionaldehyde is an enantioselective compound that can be synthesized in four steps from trichloroacetimidate and d-proline. This compound has been shown to be efficient for the olefination of aldehydes with allylic alcohols. The reaction is catalyzed by Cu(OAc)2, which is used as a catalyst to promote the reaction between the aldehyde and the allylic alcohol, leading to the formation of acetic acid esters.</p>

<p>1-(Propan-2-yl)imidazolidine-2-thione is a thione that has been shown to be a degradable molecule. It has been used in devices such as hydrogen bonding interactions, sublimable, targetable, and dispersive. The properties of 1-(Propan-2-yl)imidazolidine-2-thione make it an ideal candidate for diagnostic or therapeutic applications of iontophoresis and coordination chemistry.</p>

2-(Trimethylacetyl)thiophene is a thiophene derivative that is used as a precursor to other organic compounds. It reacts with carbon tetrachloride in the presence of light to yield 2-chloro-1,3-dithiole-4,5-dithiol and 2-trimethylacetylthiophene. The kinetics of this reaction has been studied using magnetic resonance spectroscopy. The abundances of the two products have been measured by gas chromatography/mass spectrometry (GC/MS). The dihedral angles for the reactant and product molecules have also been determined by NMR spectroscopy. This compound's conformational studies have revealed dipole moment values and frequencies that are different than those found in other thiophenes.

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Ethyl 4-oxo-5-phenylpentanoate (ETP) is a synthetic chemical that can be used as a test compound for cancer research. ETP has been shown to inhibit the growth of human breast cancer cells in vitro and in vivo. It has also been shown to have an inhibitory effect on the growth of liver cancer cells. ETP inhibits the production of endogenous retinoids, which are naturally occurring compounds derived from vitamin A, by binding to lysine residues on histones. This prevents the transcription and replication of DNA, thereby preventing cell division. The terminal half-life of this compound is approximately 1 hour in humans.</p>

<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>Benzylazepane is a triacetoxyborohydride that can be used for the reductive amination of aldehydes to form amines. Benzylazepane has been shown to react with sodium triacetoxyborohydride and amines to produce acrylonitrile, which is useful in the synthesis of polymers. The reductive amination of benzaldehyde with ethyl cyanoacetate forms acrylonitrile and acetaldehyde, which is then oxidized using ozonolysis. This reaction produces nitroethane, nitromethane, and acrylamide. Benzylazepane is also used in the synthesis of nature-inspired molecules such as polysaccharides and nucleotides.</p>

<p>Versatile small molecule scaffold</p>

<p>3,4-Dihydro-2H-1-benzopyran-4-carboxylic acid is a chromanone with an enantiomeric ratio of S:R. It is a synthetic compound and a member of the acid compounds group. 3,4-Dihydro-2H-1-benzopyran-4-carboxylic acid is used as an intermediate in organic chemistry to produce sorbinil sodium salt and ganate, which are also synthetic compounds. This chemical has been shown to be effective for oral hypoglycemia in rats when administered with amines. The racemic mixture contains two enantiomers that are not identical but are related to each other as mirror images. Phenylacetic acid (PAA) is another member of the same class of molecules that can be complicating when purified from this chemical. 3,4-Dihydro-2H-1-ben</p>

<p>Versatile small molecule scaffold</p>

<p>(1R,2S)-2-Methylamino-cyclohexanol is an alkanolamine that has been shown to have antioxidant properties. It is synthesized from hydrogen chloride and ethanolamine by a dehydration reaction. This compound can be used as a co-catalyst for the catalytic oxidation of chlorides in organic solvents and has been shown to inhibit the growth of membranes in E. coli. (1R,2S)-2-Methylamino-cyclohexanol also has potential applications in preventing atherosclerosis or treatment of zinc deficiency.</p>

<p>Versatile small molecule scaffold</p>

<p>6-Bromohexan-3-one is a pheromone that belongs to the group of skeleton-targeted pheromones. It binds to an unknown receptor in the insect and causes specific behavioral changes such as attraction, orientation, and oviposition. 6-Bromohexan-3-one has been shown to be effective against male gypsy moths, although it is not active against other insects. The structure of 6-Bromohexan-3-one consists of a phosphonium group with a six member ring and a double bond between carbons 3 and 4.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-Iodobiphenyl is a synthetic chemical compound that has been used in the manufacture of dyes, pesticides, and other organic chemicals. 3-Iodobiphenyl is a low molecular weight soluble solid with a high solubility in most organic solvents. It is insoluble in water and may be produced as one of two different isomeric forms, depending on the conditions used to synthesize it. The physical properties of these two forms are similar but they differ in their reactivity. 3-Iodobiphenyl can adsorb onto amine groups on proteins and phospholipid membranes, forming a monolayer that alters the permeability of membrane bilayers. This organocatalytic reaction can also be facilitated by metal ions such as copper or zinc. 3-Iodobiphenyl also reacts with halides such as chloride or bromide to form soluble complexes that may be used for solute separation during phase chrom</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2,4-Dimethoxyiodobenzene is a methyl ketone that has three methoxy groups. It is used as a building block in organic synthesis and can be synthesized by the reaction of 2,4-dimethoxybenzaldehyde with peroxide and methylamine. 2,4-Dimethoxyiodobenzene inhibits radical formation by reacting with an activated metal halide to form a covalent bond between the two molecules. The terminal alkyne reacts with a halogen to form an alkynyl radical which then reacts with another activated metal halide to form a second covalent bond. This process creates a new radical that has been deactivated by the addition of two bonds, preventing it from initiating another chain reaction. 2,4-Dimethoxyiodobenzene also exhibits inhibitory potency against β-amino acid decomposition through the same mechanism.</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>2,3,6-Trimethyl-1,4-naphthoquinone (2,3,6-TQ) is a hexane extract from the bark of the East Indian tree Pterocarpus marsupium that has been shown to have both reversible and irreversible inhibitory effects on monoamine oxidase. 2,3,6-TQ has been shown to have neuroprotective properties in mouse models of Parkinson's disease. It also has neurotrophic effects in cultured cells. The molecular modeling data suggest that 2,3,6-TQ binds to the active site of monoamine oxidase type A and B with a binding affinity comparable to that of clorgyline and deprenyl. In addition, it inhibits dopamine metabolism by inhibiting monoamine oxidase type A and B.</p>

<p>Methyl 3-nitropropanoate is a chemical compound that is used in synthetic organic chemistry. It can be synthesized by the nitration of propionic acid and then reacting the product with methyl iodide. This reaction produces an asymmetric synthesis of an α-lactam ring, which is one of the most commonly found functional groups in natural products. The carbonyl group on this molecule is also reactive to many other reagents, which enables it to be modified for use in various methods. The lactam ring has been shown to have anti-inflammatory properties, focusing research on its potential medicinal uses.</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>2,3-Dihydro-benzo[b]thiophen-6-amine 1,1-dioxide is a morpholine that undergoes rapid elimination to form an azepine. The compound also undergoes bromination and then subsequent debromination. The compound was found to be stable in the presence of azide, but sensitive to irradiation. Spectroscopic studies revealed that the isomers are present in equal proportions.</p>

<p>1,1-Dioxido-1-benzothien-6-ylamine is a cytotoxic drug that inhibits the synthesis of DNA and RNA in cancer cells. It is synthesized from benzo[c]thiophene-2,5-dione by oxidation with nitric acid to give the corresponding dioxido compound. The synthesized product has high lipophilicity (log P = 2.2) and a reactive hydroxy group that can undergo modifications such as esterification or alkylation. 1,1-Dioxido-1-benzothien-6-ylamine shows potent antitumor activity against solid tumours and high lipophilicity that enables it to cross the blood brain barrier very easily. It also induces apoptosis in tumour cells by binding to nucleic acids and inhibiting their synthesis. This drug is cytotoxic at nanomolar concentrations and has been shown to be effective against lung</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Ethyl 4-methylcinnamate is a ligand that binds to diazoacetate, which reacts with ethylene and aldehydes to form ethyl diazoacetate. The reaction rate increases with the addition of alkali, which causes hydrolysis of the acetal group in ethyl 4-methylcinnamate. Impurities may be present in this product, including genotoxic impurities and 8-hydroxyquinoline. Industrialized countries have strict quality control standards for this compound, whereas in developing countries, the purity of this chemical is not regulated.

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>2,4-Dichlorobenzenesulphonamide is a chlorinated benzenesulphonamide compound that has been shown to have anticancer activity. The mechanism of action is not well understood, but it has been suggested that the drug may inhibit mitochondrial membrane potential, leading to cancer cell death. 2,4-Dichlorobenzenesulphonamide has also been shown to induce apoptosis in cervical cancer cells. This drug may be useful for the treatment of carcinomas, as well as other cancers.</p>

<p>5-Methoxy-benzo[b]thiophene is a synthetic compound that has been shown to have antiestrogenic activity. It was synthesized using the acetonitrile technique and has been shown to inhibit the growth of mammary carcinomas in mice. 5-Methoxy-benzo[b]thiophene binds to estrogen receptor protein, which inhibits the binding of estrogen and prevents its effects on breast cancers. This agent also has been shown to be an effective therapy for some human breast cancer cells, which may be due to its ability to block estrogen receptor function.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2,2,6-Trimethyl-1,4-cyclohexanedione is a diketone that is produced from the shikimate pathway. It is used in organic synthesis as a carbon source and to produce volatile compounds. 2,2,6-Trimethyl-1,4-cyclohexanedione has been shown to be an attractant for mosquitoes and other insects. This compound also has pheromone activity which may be due to the presence of different isomers. 2,2,6-Trimethyl-1,4-cyclohexanedione can be found in solution form as well as in solid form with a melting point of 156°C. The compound can also be identified using various biochemical markers (e.g., esterase) or by biological studies on subcultures of bacteria or fungi.</p>

4-Hydroxy-2,2,6-trimethylcyclohexan-1-one is a subunit of the nonproteinogenic amino acid, selenocysteine. It is an intermediate in the synthesis of selenocysteine and has been shown to be stereoselective and homologous to other amino acids. 4-Hydroxy-2,2,6-trimethylcyclohexan-1-one is found in corynebacterium and thermophilic species. The enzyme dehydrogenase catalyses the conversion of this compound to 3-(3′hydroxyphenyl)-4-(4′hydroxyphenyl)butanoic acid (4HPPBA). This reaction also produces hydrogen peroxide as a byproduct. 4HPPBA can be converted back into 4-hydroxy-2,2,6-trimethylcyclohexanone by the enzyme reductase. There

<p>2-Chloro-5-(trifluoromethyl)benzamide is a profile that belongs to the group of anti-tuberculosis drugs. It has a high cytotoxic effect against eukaryotic cells and has been shown to have an anti-tuberculosis effect in mice. 2C5BM also inhibits bacterial growth by binding to DNA gyrase and topoisomerases, thereby inhibiting the replication of bacteria. Studies have found that 2C5BM can inhibit the growth of Mycobacterium tuberculosis, but not Mycobacterium avium complex. The therapeutic index for 2C5BM is high, which means it has a wide range of safety margins, with no detectable side effects on healthy human erythrocytes.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Spiro[2.3]hexan-4-one is a reactive, hydrophobic molecule that is synthesized by the reaction of an epoxide with an alcohol. This compound has been shown to undergo photooxidation and thermally induced reactions. It can be used in coatings to provide resistance to environmental effects such as hydrolysis, oxidation, or photooxidation. Spiro[2.3]hexan-4-one can also be used in the production of methylenecyclopropanes, which are used as chemical intermediates for pharmaceuticals and other organic compounds.

<p>Versatile small molecule scaffold</p>

<p>4-Methyl-1,5,6,7-tetrahydro-2H-cyclopenta[b]-pyridin-2-one is a cycloalkane that has been shown to have antiinflammatory properties. It has been found to produce phosphoric acid and methanol when heated in the presence of phosphoric acid. 4-Methylcyclohexanone has also been shown to form hydrogen bonds with a variety of molecules including other cycloalkanes, nitro compounds, aromatic hydrocarbons, and heterocyclic compounds. Single crystal x-ray diffraction studies of this compound have revealed that it adopts an anisotropic molecular structure.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Methyloct-3-yn-2-ol is a nucleophile that can be used to make an efficient method for the synthesis of olefinic bonds. This compound is also a ligand, which can form bidentate complexes with electrophilic metal centers. 2-Methyloct-3-yn-2-ol has been shown to react with heterocycles and alkenes in nucleophilic addition reactions. The reaction mechanism is thought to proceed through c–h bond cleavage, followed by dehydration of the resulting olefinic products. This process is reversible and can be driven by acid or base catalysis.</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Bromo-1-methylnaphthalene is the chemical compound with the formula C6H5BrCH2. It is a brominated derivative of naphthalene. This compound is an intermediate in the synthesis of arylboronic acids, which are used as coupling partners in Suzuki and Miyaura cross-coupling reactions. It also has been used as a catalyst for indole synthesis from chlorobenzene and ammonia. 2-Bromo-1-methylnaphthalene can be prepared by treating naphthalene with bromine and potassium t-butoxide at low temperature. The reaction can also be conducted using chloride or potassium instead of t-butoxide.<br>2-Bromo-1methyhnaphthalene is a useful chemical because it can react efficiently with aryl bromides to produce coupling products, such as benzofuran derivatives, in high yield.</p>

<p>Versatile small molecule scaffold</p>

<p>N-Aminobenzenecarbothioamide is a chemical compound that is stable in hydrochloric acid and carbon disulphide. It has been shown to inhibit the growth of skin cells by binding to epidermal growth factor. It also inhibits the production of inflammatory bowel disease, which may be due to its ability to inhibit nitro and nitrite ion. The antimicrobial activity of N-aminobenzenecarbothioamide has not been studied.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-Bromo-2-methylpropanoic acid is a colorimetric substrate that is used in the screening of enzymes with propionate as a cofactor. This substrate has been found to be selective for esterases, and can be used as an alternative to octanoate for enzymatic studies. The 3-bromo-2-methylpropanoic acid esters are also hydrophobic and have higher melting points than their corresponding acids, making them more suitable for thermophilic organisms. <br>The 3-bromo-2-methylpropanoic acid esters are chiral compounds that can be synthesized in two forms: (R)-3-bromo-2-methylpropanoic acid methyl ester and (S)-3-bromo-2-methylpropanoic acid methyl ester. The enantiomers of these compounds exhibit different biological activity. For example, the (S)-enantiomer</p>

<p>Ethanol, 2-(phenylsulfonyl)- is a synthetic chemical compound. It is used as an electron donor in the Suzuki coupling reaction and has shown significant cytotoxicity against tumour cell lines. This product also has been used in the synthesis of naphthalene and pulchella. The mechanism for its cytotoxicity involves the desulfurization of tyrosinase, which is an enzyme that catalyzes the conversion of dihydroxyphenylalanine to melanin. This product has also been shown to be effective against glandularia with structural studies showing that it reacts with sulfonic acid groups.</p>

<p>Versatile small molecule scaffold</p>

<p>3-tert-Butylcyclobutanone is an organocatalyst that is used for the asymmetric synthesis of cyclobutanones. It has been shown to be a chiral, stereoselective and catalytic mediator in the Baeyer–Villiger oxidation of enones. 3-tert-Butylcyclobutanone also exhibits self-assembly properties and can form dimers with other molecules. This compound is also capable of catalyzing cycloadditions between electron deficient alkenes and electron rich dienes. The dimers of 3-tert-butylcyclobutanone are formed by hydrogen bonding interactions between the keto groups on adjacent molecules.</p>

<p>3,3-Dimethyl-5-oxohexanoic acid is a peroxide with the chemical formula C10H16O4. It is synthesized by the ozonolysis of isophorone. 3,3-Dimethyl-5-oxohexanoic acid can be used as a dehydrating agent and has been shown to be effective in the production of esters, such as methyl esters. The dehydration of this compound gives rise to hydrogen peroxide and acetone. The hydrolysis of 3,3-dimethyl-5-oxohexanoic acid with water yields acetic acid and methyl alcohol. This reaction has been shown to be stoichiometric.</p>

<p>1-(2-Methoxy-5-methylphenyl)ethanone is a volatile, synthetic compound. It is used as a chemical intermediate in the production of picotamide and esterification products. Methoxyphenylacetic acid (1) is methylated with methanol in the presence of hydrochloric acid to form 2,5-dimethoxybenzoic acid (2). The latter is then esterified with methanol and acetic anhydride to yield picotamide (3).</p>

<p>Versatile small molecule scaffold</p>

<p>3-Ureidobenzoic acid is an organic compound that can act as a reducer or bidentate ligand. The reductive properties of 3-ureidobenzoic acid are due to its ability to accept electrons from other molecules, which can be used to reduce metal ions. The ligand properties of 3-ureidobenzoic acid are due to the formation of a covalent bond with other molecules, often metal ions. 3-Ureidobenzoic acid is also known to be a synthetase, which catalyzes the formation of peptide bonds in proteins by joining amino acids together. This compound has been found in cytochrome P450 enzymes, where it is believed to play a role in electron transfer and activation reactions. It has also been shown to be involved in supramolecular hydrogen bonding, which stabilizes certain compounds and plays an important role in enzyme activity and intermolecular reactions.</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>1-Butyl-4-nitrobenzene is an environmental pollutant that is a byproduct of coal combustion and industrial processes. It can be chlorinated to produce 1,2,3-trichloropropane, which is used in the production of various chemicals. The chemical transformation of 1-butyl-4-nitrobenzene yields a variety of products including nitroarenes and anilines. The mechanistic pathways for the production of these compounds are not completely understood but it has been shown that isotope effects may play a role in the formation of certain product yields.</p>

<p>2,2-Dimethylpentanenitrile is a solvent that can be used in the polymerization of cellulose acetate. It has been shown to have reactive sites and be resistant to radiation and heat. 2,2-Dimethylpentanenitrile has also been used as a polymerization initiator for cationic polymers, which are water vapor-resistant and bond cleavage resistant. This compound is an experimental infection agent that is used against enteritidis, which is an antibiotic-resistant bacterium. 2,2-Dimethylpentanenitrile has also been shown to be effective as an electrophotographic developer for particle suspensions and gaseous emissions.</p>

<p>2-Methyl-4-phenyl-1,3-oxazole is an organic compound that is a white solid. It has a molecular weight of 222.2 g/mol and chemical formula C6H5NO2. 2-Methyl-4-phenyl-1,3-oxazole can be synthesized by reacting phenylmagnesium bromide with methyl iodide in an ether solvent at room temperature. The reaction produces a product in high yield, which is soluble in both water and organic solvents. The product is stable to air and light for up to two months at room temperature.<br><br>The following are the properties of 2-methyl 4 phenyl 1,3 oxazole:<br><br>• White solid<br>• Molecular weight of 222.2 g/mol<br>• Chemical formula C6H5NO2 <br>• Soluble in both water and organic solvents <br>• Synthesized by reacting phenylmag</p>

<p>Versatile small molecule scaffold</p>