Building Blocks

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>IR-780 iodide is a water-soluble drug that has been shown to have significant cytotoxicity against prostate cancer cells. It binds to the mitochondrial membrane potential, which is involved in energy production and the regulation of the cell cycle. IR-780 iodide is taken up by tumor cells, where it inhibits adriamycin uptake and induces apoptosis. In vitro assays have shown that IR-780 iodide can be used as a diagnostic tool for detecting bladder cancer by binding to the mitochondria of cells from patients with bladder cancer. In vivo studies have been done in mice to determine the effectiveness of IR-780 iodide in treating cervical cancer. These studies showed that IR-780 iodide was not significantly effective in vivo, due to its low bioavailability and lack of specificity for cervical cancer cells. Histological analysis showed that IR-780 iodide did not inhibit tumor growth or induce apoptosis in vivo.</p>

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about H-D-ASN-L-ASP-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Iodobenzoic acid methyl ester is a palladium complex that can be used as a catalyst for the hydrolysis of ketoesters, imines, and halides. The reaction mechanism involves the coordination of the metal center to the carboxylate or amine group on the substrate, followed by a nucleophilic attack at the benzoate or chloride group. The resulting product is an alkyl halide. 2-Iodobenzoic acid methyl ester has been shown to catalyze the cross-coupling of diphenyl ethers with various amines in water and in organic solvents.</p>

<p>Versatile small molecule scaffold</p>

<p>2-Iodobenzoic acid is a synthetic compound that is used in the treatment of wastewater. It is produced by the reaction of benzoate and nitrite in the presence of sodium hydroxide. The intramolecular hydrogen atom transfer from the 2-iodobenzoic acid to benzoate is a reversible reaction. This process can be catalyzed by palladium, which has been shown to be effective in coupling 2-iodobenzoic acid with other compounds to produce cyclic peptides. The use of 2-iodobenzoic acid as a contraceptive has been investigated for its ability to inhibit acetylcholinesterase activity, which may lead to increased levels of acetylcholine and inhibition of muscle contractions.</p>

<p>Isocytosine is a prodrug that has been synthesized with the intramolecular hydrogen on the nitrogen atoms, which makes it more chemically stable. Isocytosine is a reactive molecule, and can react with tautomers to form isocytosine derivatives. Isocytosine contains three hydrogen atoms that are transferable through reactions to other molecules. The chemical stability of isocytosine allows for its use in wastewater treatment. It also has metabolic effects, such as the inhibition of colorectal adenocarcinoma and metabolic disorders. Isocytosine can be used as a model system for studying transfer reactions and reaction mechanisms.</p>

<p>Prop-1-en-2-ylboronic acid is a chemical compound that belongs to the group of aromatic hydrocarbons. It is used in pharmaceutical preparations as a monomer and as a chiral building block for the synthesis of oxazolidinones, which are used in medicinal chemistry as protein inhibitors against cancers. Prop-1-en-2-ylboronic acid is also used as a reagent in preparative high performance liquid chromatography. This chemical has shown maximal response against colorectal carcinoma cells and has been shown to be an inhibitor of cholesterol ester transfer.</p>

<p>(6,6)-Phenyl-C61 butyric acid methyl ester (PCBM) is an organic semiconductor that has been used in molecular modeling studies and experimental models. The molecular structure of PCBM consists of a phenyl group on one end and a butyrate group on the other end. It has been shown that PCBM can be used to create polymer films with enhanced UV absorption properties. These films can be used as reaction products for low energy transport properties. This organic semiconductor is also known to have a high efficiency when it comes to cycloaddition processes, which can be achieved by multi-walled carbon nanotubes. PCBM has been shown to have a morphology that includes spherical particles with diameters between 10 and 20 nm.</p>

<p>Pent-4-enylamine is a nitrogen nucleophile that can react with alkenes to form compounds. Pent-4-enylamine reacts quickly with alcohols and ethers in the presence of an acid catalyst to produce an alkene. Pent-4-enylamine has been used in food chemistry as a reactive intermediate for the formation of functional groups, such as amines, hydroxyl groups, and nitriles. It is also a model system for studying aminoalkenes and their reactions with other functional groups. Pent-4-enylamine has been shown to be a reactive heterocycle that forms 5 membered heteroaryl rings using structural analysis and model system studies.</p>

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about Octahydro-2,6-naphthyridin-1(2H)-one acetate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 10-Oxooctadecanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 5-(1-Oxodithiolan-3-yl)pentanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Mercapto-N-methylbenzamide is a synthetic compound that has been shown to have inhibitory activities against activated brain cells and cell lines. This drug has been used in the synthesis of axitinib, a cancer drug that inhibits cellular growth. 2-Mercapto-N-methylbenzamide is also used as a preservative in cosmetics and can be found in carbonated drinks and foods. It has been shown to inhibit the production of serotonin in microbicidal reactions by inhibiting the enzyme hydroxymethyl transferase, which catalyzes the conversion of 5-hydroxytryptophan to serotonin. It also prevents the reaction products from being formed by reacting with hypoxanthine, xanthine, and phosphoribosyl pyrophosphate (PRPP). 2-Mercapto-N-methylbenzamide also reacts with plasma samples to form ethylmercaptoacetate, which is then oxidized to merc</p>

<p>Organic intermediate</p>

<p>2,4,6-Triphenylpyridine is an aromatic heterocycle with a benzyl group and trifluoroacetic acid at the 2-, 4-, and 6-positions. It is a colorless solid that has a melting point of 183 °C. In the gas phase, it exists as three anion radicals (2-, 4-, and 6-). These radicals are responsible for its optical properties. The 2-anion radical has a blue emission spectrum while the 4- and 6-anion radicals have red emission spectra. 2,4,6-Triphenylpyridine can be used as an indicator for trifluoroacetic acid or benzonitrile. It is soluble in primary alcohols such as methanol and ethanol at lower temperatures, but becomes insoluble at higher temperatures. 2,4,6-Triphenylpyridine also has functional theory applications due to its ability to</p>

<p>3-Hydroxynaphthalene-2-carboxaldehyde is a primary amino acid that can exist in two forms, the imine and the enamine tautomers. The proton on carbon 2 is acidic, which allows for hydrogen bonding with other molecules. The 3-hydroxynaphthalene-2-carboxaldehyde has a viscosity of 1mm2/s and a fluorescence emission maximum at about 275nm. It also has optical properties that are similar to naphthalene.</p>

<p>Please enquire for more information about 3-(Prop-2-en-1-ylsulfanyl)prop-1-ene including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>6-Bromo-2-methoxyquinoline is a versatile compound with various applications. It is commonly used as a disinfectant in ceramic compositions and research chemicals. Additionally, it has been found to have potential therapeutic benefits. Studies have shown that 6-Bromo-2-methoxyquinoline exhibits antioxidant properties and can inhibit the production of inflammatory mediators such as arachidonic acid and prostaglandins. Furthermore, it has been found to modulate potassium channels, which play a crucial role in cellular function. This compound also shows promise in the development of copolymers and other materials due to its unique chemical structure. With its wide range of applications, 6-Bromo-2-methoxyquinoline is an essential compound for various industries.</p>

<p>Diethyl Acetylphosphonate is a synthetic chemical that is used in the production of ethyl esters, which are used as intermediates for the production of epoxides. It has shown to be a bidentate ligand and reacts with primary amines. Diethyl Acetylphosphonate can be made by reacting phosphorus pentachloride with ethyl acetate and hydrochloric acid. The reaction mechanism is similar to that of other organophosphorus compounds, in which a phosphine oxide intermediate reacts with an organic halide. Diethyl Acetylphosphonate has shown to be effective in detergent compositions and triethyl orthoformate, as well as alkanoic acid.</p>

<p>Versatile small molecule scaffold</p>

<p>4,4'-Dithiopyridine is a reactive molecule that can be used in the synthesis of other organic compounds. It is a disulfide bond with a redox potential of -0.43 V, which makes it readily available for reaction. The structural analysis of 4,4'-dithiopyridine has been performed using NMR spectroscopy and gas chromatography/mass spectrometry (GC/MS). This compound is an inhibitor of sugar transport and can be used to study the p-nitrophenyl phosphate reductase enzyme in bacteria. The reaction product between 4,4'-dithiopyridine and NADPH cytochrome P450 produces the fluorescent molecule 2-aminopurine. This fluorescent molecule may be used as a probe to study transfer reactions in bacteria.</p>

<p>Diiodomethane is a chemical compound with the molecular formula CHI. It is a colorless gas that can be obtained by reacting methyl ethyl and hydroxyl group in the presence of an oxidant such as boron nitride. Diiodomethane has been used as a substrate film for n-dimethyl formamide and reaction solution, which have been studied using spectroscopic data. The product of this reaction is water vapor that leaves the system due to its low boiling point. Reaction mechanism for this process is thought to be due to the kinetic energy of the particles that collide and produce diiodomethane molecules.</p>

<p>2,4-Dibromothiazole is a nicotinic acetylcholine receptor (nAChR) antagonist which selectively blocks the binding of acetylcholine to nAChRs. It has been shown to be effective in treating inflammatory bowel disease by inhibiting the production of inflammatory mediators. This drug also has anti-inflammatory effects and can be used for the treatment of autoimmune diseases such as Crohn's disease. 2,4-Dibromothiazole also has low energy properties and is used in palladium complexes for cross-coupling reactions. It can also be used as a cancer chemotherapeutic agent and as a cardiac drug.</p>

<p>4,6-Dichloro-5-nitropyrimidine is an intermediate in the synthesis of Tenofovir, a nucleophilic drug that inhibits HIV. It is produced by the reaction of chloride with amines and nitro compounds in the presence of ammonium chloride. 4,6-Dichloro-5-nitropyrimidine has been shown to have anticancer activity against human lymphocytes and other cancer cells. It can also be used for the treatment of AIDS. The biological properties of this compound are dose dependent and are dependent on the size of chlorine atoms attached to nitrogen atoms.</p>

<p>2,4-Diamino-5-nitropyrimidine is a synthetic molecule that belongs to the class of heterocyclic amines. It has been shown to be a potent antiproliferative agent and has been found to inhibit hepg2 cell growth in vitro. This compound was also found to inhibit cancer cells, including mcf-7. 2,4-Diamino-5-nitropyrimidine binds nucleophilic sites on proteins and inhibits enzymes involved in DNA synthesis. The inhibition of these enzymes leads to cell death by preventing the production of new proteins needed for cell division.</p>

<p>3-Chloro-5-iodobenzoic acid methyl ester is a versatile building block that can be used to make many complex compounds, including research chemicals and reagents. 3-Chloro-5-iodobenzoic acid methyl ester is used as an intermediate for the production of speciality chemicals and has many uses in chemical reactions. This compound was previously sold under the CAS number 289039-85-6.</p>

<p>(-)-Corey lactone diol is a synthetic compound that is soluble in organic solvents. It is used for the synthesis of carbocyclic nucleosides, which are analogs of pyrimidine nucleosides. (-)-Corey lactone diol has been shown to inhibit cholesterol synthesis and the synthesis of alkene. (-)-Corey lactone diol also shows anti-inflammatory properties, which may be due to its inhibition of prostaglandin synthesis.</p>

<p>4-Chloro-8-quinolinol is a quinoline derivative that has been shown to have pharmacological effects. It is used in the synthesis of other compounds, such as 5-chloro-8-hydroxyquinoline, which is used in the treatment of cancer. 4-Chloro-8-quinolinol can also be prepared by oxidizing 5,6,7,8 tetrachloroquinoline with chlorine and ammonia. The photophysical properties of this compound are analogous to those of benzothiazole derivatives. The fluorescence emission spectrum ranges from 360 nm to 450 nm with a maximum at 390 nm and emission intensity at 350 nm. This compound exhibits fungitoxicity against Penicillium notatum and Aspergillus fumigatus.</p>

<p>Cyclobutanesulfonyl chloride is a reagent that is used for the synthesis of 1-6-alkylcyclobutanes. It can be used to synthesize heterocyclic compounds, including those with high optical purity. Cyclobutanesulfonyl chloride has been shown to have antiviral and antiproliferative properties. It has also been shown to exhibit anticancer activity in vitro and in vivo. The mechanism of action for this compound is unclear, but it may inhibit protein synthesis by attacking the amino acid methionine in proteins or by inhibiting DNA replication.</p>

<p>Chloroiodomethane is a chemical that is used as an intermediate in the production of other chemicals. It is a colourless liquid with a strong odour. 3-Bromopropylamine hydrobromide reacts with chloroiodomethane to form 3-bromopropyl bromide, which can be reacted with hydrogen chloride to form the corresponding acid chloride. This reaction product can then be reacted with β-amino acids to form amides or esters. The reaction mechanism of this process involves nucleophilic substitution of chloroiodomethane by the amino group of the β-amino acid to produce an intermediate α,β-unsaturated carbonyl chloride, which undergoes elimination to give the final product. Chloroiodomethane also reacts rapidly with fatty acids and hydroxyl groups in biological systems, leading to inflammatory diseases such as HIV infection.</p>

<p>4-tert-Butoxybenzaldehyde is a colorless liquid that has a viscosity of 0.3 mm2/s at 25 °C. It can be synthesized by reacting pyridine with hydrochloric acid in the presence of a Grignard reagent. 4-tert-Butoxybenzaldehyde reacts with phenolic antioxidants to form an ester, which can be used as an industrial solvent. The crystal x-ray diffraction pattern of 4-tert-Butoxybenzaldehyde exhibits peaks at 2θ = 8.0, 11.5, and 18.5° corresponding to the (100), (200), and (220) planes, respectively. This chemical can also undergo reactions that lead to termination or transfer reactions, including diethyl ketomalonate formation with diethyl malonate in the presence of water as a solvent and potassium hydroxide as a catalyst for transfer reactions.END&gt;</p>

<p>1,4-Benzenedicarboxylic acid, monoethyl ester (1,4-BDE) is a monomer that is used in the manufacture of polycarbonates and other plastics. 1,4-BDE is also used as a solvent for xylene and butanol. It has been shown to be useful in the production of polyester fibers. The monomer can be synthesized by reacting ethylene with terephthalic acid or dimethyl terephthalate (DMT). This reaction produces 1,4-BDE and methanol as byproducts. The process is carried out at temperatures of 250 °C to 300 °C and under atmospheric pressure. The purified product can be isolated using distillation or extraction with organic solvents such as benzene or butanol. The reaction can be carried out in the presence of ruthenium, which acts as a catalyst.</p>

<p>2-(Boc-aminomethyl)benzoic acid is a versatile building block with a wide range of applications in the field of organic chemistry. It has been shown to be useful as a reagent in the synthesis of complex compounds and fine chemicals, as well as a reaction component for the preparation of pharmaceuticals. 2-(Boc-aminomethyl)benzoic acid can also be used as an intermediate in the synthesis of speciality chemicals such as herbicides, pesticides, and fungicides.</p>

<p>Please enquire for more information about N-[5-(4-Bromophenyl)-6-(2-hydroxyethoxy)-4-pyrimidinyl]-N′-propylsulfamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Benzofuran-5-carbaldehyde is a synthetic compound that inhibits the enzyme ido1. It has been shown to have potent cytotoxicity, potent inhibition, and neurotrophic properties in a number of cell lines. 1-Benzofuran-5-carbaldehyde also exhibits inhibitory effects on the enzymes hydrolyzing dopamine, which is involved in the synthesis of norepinephrine and epinephrine. The chemical structure of 1-benzofuran-5-carbaldehyde closely resembles that of dopamine and its derivatives, and can be used for the treatment of neurodegenerative diseases such as Parkinson's disease.</p>

<p>4-Bromobenzaldehyde is a chemical compound that belongs to the group of aromatic compounds. It has been shown to have a potent stimulatory effect on locomotor activity in mice, which may be due to its ability to increase levels of epidermal growth factor and gamma-aminobutyric acid in the brain. 4-Bromobenzaldehyde can be synthesized from 2,4-dibromophenol and anhydrous copper chloride in the presence of sodium hydroxide. The reaction mechanism for this synthesis is believed to involve an intermediate enamine form of 4-bromobenzaldehyde, which can then undergo hydrolysis into 2,4-dibromophenol and benzaldehyde. This product is used as a reagent in organic synthesis because it can be used to form esters with trifluoroacetic acid or hydrochloric acid in high yield.</p>

<p>Please enquire for more information about 5-Bromo-2-fluoro-1,3-dimethylbenzene including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-Chloropyrimidine-2-carbonitrile is an industrial chemical that belongs to the class of heterocycles. It is commonly used in the synthesis of amines, phenoxy compounds, and halides. This compound is widely used in research laboratories as a building block for the synthesis of various organic compounds. 4-Chloropyrimidine-2-carbonitrile is available in enantiopure form, making it suitable for chiral chemistry applications. It contains cyano and ethoxycarbonyl functional groups, which make it versatile for further derivatization. This compound exhibits solid catalyst properties and can be used as a methyl ether or amide precursor. Its emission properties make it useful in fluorescence-based assays and imaging techniques.</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 methanesulfonate is a genotoxic agent that inhibits the growth of bacteria by binding to the DNA. N-butyl methanesulfonate is effective against typhimurium and has shown carcinogenic effects in hamster cells. N-butyl methanesulfonate is also capable of inhibiting quinoline derivatives, which are carcinogens that are found in tobacco smoke. This chemical can be used as a natural compound for the treatment of diabetic neuropathy and cryptococcus neoformans. It may also be used as an antiviral agent for the treatment of influenza virus.</p>

<p>Versatile small molecule scaffold</p>

<p>Bromo-PEG3-azide is a PEG compound with two different functional groups (also known as heterobifunctional). Unlike homobifunctional PEG compounds (same functional group on both ends), this type of compounds are more versatile as have two different anchor points. Bromo-PEG3-azide is used as a linker and spacer to add a PEG moiety, via pegylation (a bioconjugation technique) to proteins, peptides, oligonucleotides, small molecules and nanoparticles.</p>

<p>2-Bromo-3-hydroxy-benzaldehyde is a nitrate that has been shown to have anti-cancer properties. It inhibits the growth of cancer cells by binding to bromodomains in their DNA, thereby preventing transcription and replication. 2-Bromo-3-hydroxy-benzaldehyde also inhibits the production of nitric oxide, which may lead to an inhibitory effect on tumour angiogenesis. The stereoisomers of this compound are used as precursors for the synthesis of ammonium nitrate, which is used as a fertilizer and explosive. 2-Bromo-3-hydroxy-benzaldehyde is also used in organic synthesis as a precursor for acetylation or halide reactions with palladium complexes or halides.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-Ethyl-4-methylpyrrole-2,5-dione is a chlorophyll analog. It has been found to be an electron donor in photosystem II of the chlorobium reaction center. The compound was prepared by evaporation of a solution of chlorobenzene and ethyl acetoacetate in carbon tetrachloride with the aid of a vacuum pump. 3-Ethyl-4-methylpyrrole-2,5-dione has also been used as a reagent for the preparation of phycocyanin from Spirulina platensis, which is an important component of blue algae. The compound reacts with phenoxy and furyl groups under acidic conditions to produce carboxylate and calcium carbonate, respectively. Oxidation products are formed in reactions with ethyl group and other organic compounds under alkaline conditions.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1-Bromo-4-isobutylbenzene is a ketone that can be synthesized by the reaction of benzene with acetonitrile in the presence of a catalytic amount of oxone. The synthesis is an example of an arylation, which is the addition of an aromatic group to another molecule. It has been shown experimentally that 1-bromo-4-isobutylbenzene undergoes a transition from the x-ray structure analysis to the crystal x-ray structure when dissolved in acetonitrile and heated to 100°C. The final product is then purified by recrystallization with ethylene as a solvent.</p>

<p>Glycidyltrimethylammonium chloride is a quaternary ammonium compound that has been widely used as a disinfectant and in wastewater treatment. It is mainly used to kill bacteria and viruses, although it can also be used to remove hazardous material from water. Glycidyltrimethylammonium chloride has the ability to inhibit bacterial growth by causing cell membrane damage. This compound is also able to inhibit the synthesis of DNA, RNA, and protein in cells by binding to their respective building blocks. In addition, glycidyltrimethylammonium chloride has cytotoxic effects on human cells and significantly inhibits the replication of oral pathogens.</p>

<p>Versatile small molecule scaffold</p>

<p>3-Methylbenzo[b]thiophene-2-carboxylic acid (MBTCA) is a heterocyclic compound that is an intermediate in the synthesis of 3-methylthiophene-2-carboxylic acid, a precursor to other drugs. MBTCA is an aerobic, nonpolar compound that has shown antimicrobial activity against some bacteria and fungi. It also has been shown to have practicality as a biomolecular probe for methyl groups in organic solvents. MBTCA can be synthesized by nitration of benzene in the presence of sulfur and sulfoxides. This reaction produces nitrobenzene, which can then be oxidized by potassium permanganate or hydrogen peroxide to produce MBTCA. The most common isomer of MBTCA is 2-(3,5-dimethoxybenzylidene)tetrahydrofuran, with three methyl groups on the</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>3,4,5-Trimethoxybenzoyl Chloride is a reactive, active chemical that is used in the synthesis of cytotoxic amides. It is prepared by reacting 3,4,5-trimethoxybenzoic acid with an amine or ammonia in the presence of a base. The reaction yields an amide substituted at the 3- and 4-positions with trimethoxyphenyl groups.</p>

<p>Versatile small molecule scaffold</p>

<p>p-Isobutylstyrene-d7 is a solid catalyst that can be used in the synthesis of organic compounds. It has been shown to have good activity for the transfer of acid chloride groups to aromatic ring systems and for the synthesis of thiadiazoles. p-Isobutylstyrene-d7 has been shown to be an excellent catalyst for the conversion of hydrochloric acid into hydrogen chloride, which can then be recycled. The toxicity studies on this compound have shown that it is not toxic to bacterial strains, which may make it a good candidate for use as a catalyst in bioremediation or a growth substrate. This catalyst has also been shown to have photocatalytic activity and may be used in the purification of water contaminated with heavy metals.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Ethyl 3-formyl-1H-pyrrole-2-carboxylate is a formyl compound with the molecular formula C8H8O3. It is a colorless liquid that has a strong odor. The compound can be obtained by the reaction of ethyl acetoacetate and pyrrole in the presence of aluminum chloride. The compound has been studied for its nuclear magnetic resonance (NMR) properties. It has two conformers, which are distinguished by their different chemical shifts, and this difference can be used to study coupling between the carbonyl group and other groups in the molecule.</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>3-Bromo-2-nitrobenzaldehyde is an organic chemical compound used in the synthesis of other chemical compounds. It is a colorless liquid that can be easily synthesized using potassium permanganate, tetrahydrofuran, acetone and hydrochloric acid. The chemical reaction is carried out by reacting potassium permanganate with hydrochloric acid to form potassium chloride and manganese dioxide. The manganese dioxide then reacts with acetone to produce 3-bromo-2-nitrobenzaldehyde. This synthetic method for producing 3-bromo-2-nitrobenzaldehyde uses less hazardous chemicals than the traditional method.</p>