Building Blocks

<p>Versatile small molecule scaffold</p>

<p>Fmoc-Ala-Ala-Pro-OH is a building block that is used in organic synthesis as a reaction component or reagent. It can be used to synthesize a wide range of complex compounds with speciality chemical and fine chemical applications. Fmoc-Ala-Ala-Pro-OH is also a versatile building block that can be used to synthesize various useful scaffolds, such as the Fmoc amino acid sequence, which has been shown to bind heparin. This compound has high purity and can be used in research and development.</p>

<p>Fmoc-b-Ala-Phe-Pro-OH is a chemical compound that is used as a reaction component, reagent, and useful scaffold. It reacts with various other chemicals to form complex compounds. This synthetic compound can be used as an intermediate in the synthesis of peptides, proteins, and other organic compounds. Fmoc-b-Ala-Phe-Pro-OH can also be used as a building block for the synthesis of speciality chemicals.</p>

<p>3,4-Difluoro-1H-Pyrrole is a neutral compound with a molecular weight of 136.17 g/mol. It has the chemical formula C6H3F2N and it can be found in reactions involving the congener and coordination chemistry. 3,4-Difluoro-1H-Pyrrole is an intermediate in organic synthesis that is used as starting material for other organic compounds such as pharmaceuticals and agrochemicals. The redox potential of 3,4-Difluoro-1H-Pyrrole is -0.42 V for the reaction with chloride solution and its basicity is 0.89 mM at 25°C. This molecule has been studied by X-ray crystallography and by titration calorimetry for hydrogen bonding interactions.</p>

<p>3,5-Dimethylbenzaldehyde is an organic compound that is a colorless liquid. It has a chemical formula of C9H12O2 and is classified as an aldehyde. 3,5-Dimethylbenzaldehyde can be synthesized by the reaction of isopropyl palmitate with xylene in the presence of carbon as a source. The reaction time required for this synthesis is approximately one day. The major products of this reaction are 3,5-dimethylbenzaldehyde and 2-methylbutanal. This reaction mechanism can also be used to determine the concentration of urinary metabolites in human urine samples. Analysis of these samples requires an organic solvent such as hexane or dichloromethane. Kinetic data was collected from the rate at which zinc powder reacts with 3,5-dimethylbenzaldehyde over time at different concentrations. A kinetic experiment was conducted using c–h bond activation to produce 3,5-dimethoxy</p>

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about 6-(Chloromethyl)pteridine-2,4-diamine monohydrochloride 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 N-[2-[(2S)-2-Cyano-4,4-difluoro-1-pyrrolidinyl]-2-oxoethyl]-6-[methyl[3-(1-piperazinyl)propyl]amino]-4-quinolinecarboxamide trifluor oacetate 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 D-Carnosine trifluoroacetate 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 (αR)-α-(2-Chlorophenyl)-2H-tetrazole-2-ethanol  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 4-Chloro-N-[2-(1,2-dihydro-2-oxo-4-quinolinyl)ethyl]benzamide 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 Cyanidin 3-O-rutinoside 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>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-[[(3aS,4R,6S,6aa)-4-[7-[[(1R,2S)-2-(3,4-Difluorophenyl)cyclopropyl]amino]-5-(propylthio)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-3-yl]- 2,2-dimethyl-tetrahydro-3aH-cyclopenta[d][1,3]dioxol-6-yl]oxy]ethanol-d7 is a compound with brominated sparfloxacin. It has various applications in the field of biochemistry and research chemicals. This compound has been found to have interactions with adipocytes and adipose tissues. Additionally, it has shown potential effects on glycan metabolism and potassium ion channels. Furthermore, this compound has been studied for its potential as an herbicide and its interaction with other substances such as</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1-Phenyl-1H-pyrazol-4-amine is a white crystalline solid that can be used in organic synthesis. It is soluble in water and acetone, but insoluble in ether and chloroform. The chemical formula for 1-phenyl-1H-pyrazol-4-amine is C6H5N3O. It has a molecular weight of 147.17, an empirical formula of C6H5N3O and a density of 1.47g/mL at 20°C. 1-Phenyl-1H-pyrazol-4-amine reacts with the hydroxyl group on l -glutamic acid to form the corresponding ester, which can be hydrolyzed under alkaline conditions to produce ammonia and benzoic acid. This molecule also contains an anion that can be deprotonated by an alkali metal such as sodium or potassium to form the corresponding salt, which</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2,2-Dipropylpentanoic acid is a white crystalline solid with a melting point of -51°C. It has a hydroxyl group and an ester linkage. The chemical formula is CH3(CH2)3COOC3H7. It has a molecular weight of 182.27 g/mol and a density of 1.071 g/cm3. It is soluble in organic solvents such as chloroform, ether, benzene, acetone, and carbon tetrachloride but insoluble in water. 2,2-Dipropylpentanoic acid can be used as a catalyst for the synthesis of polymers from monocarboxylic acids and chloride or magnesium halides. This compound also has antidepressant activity by inhibiting the reuptake of serotonin from the synapse into the presynaptic neuron.</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>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>2,6-Dimethylphenylacetic acid is a hydrogen phosphate that is soluble in solvents such as acetonitrile. It has been used in the synthesis of lidocaine with high sensitivity and specificity. It can be used to detect phosphoric compounds, which are often present in pharmaceuticals and food supplements. This compound has also been shown to have a solvent effect on the conditions of the reaction, making it a useful additive for optimizing processes. The main impurities of this compound are 2-methylbenzoic acid and benzoic acid.</p>

<p>Versatile small molecule scaffold</p>

<p>2-Methylthiazole-4-carboxaldehyde is an aldehyde that is the product of the condensation of 2,4-dibenzoylacetone and acetone in the presence of diazomethane. It has been used as a precursor to other compounds such as benzoyl chloride, glyoxal, and aldehydes. 2-Methylthiazole-4-carboxaldehyde can be synthesized using acetylation or nitration of thiols or with glyoxal or aldehyde. The reactivity of this compound is high and can be carried out in high yield.</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>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Iridium(III) bis-(2-phenylpyridine) (Ir{dFCF3ppy}2(bpy)) is a monomeric amido ligand that can be used in polymerization processes. It has an average molecular weight of 185.8 and a transition temperature of -55°C. Ir{dFCF3ppy}2(bpy) is soluble in organic solvents such as chloroform and acetone and will react with amines, anionic sites, and cycloalkyl groups to form polymers. The yields of the polymerization process are dependent on the starting materials used.</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>Tadalafil is a synthetic drug that is used as a treatment for erectile dysfunction. It works by inhibiting the PDE5 enzyme, which is responsible for breaking down cGMP. Tadalafil has been shown to be effective in the treatment of male erectile dysfunction and pulmonary hypertension, with few side effects. This drug is taken orally, with a meal or without one, and can be administered with or without food. To improve absorption, tadalafil should be taken at least 30 minutes before sexual activity. The dosage of tadalafil ranges from 2.5 to 20 mg, and it should not exceed 40 mg per day.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about (2R,4R)-1-[(2S)-5-Amino-1-oxo-2-[[(1,2,3,4-tetrahydro-3-methyl-8-quinolinyl)sulfonyl]amino]pentyl]-4-methyl-2-piperidinecarboxylic a cid 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 (R)-1-[3-[4-Amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]piperidin-1-yl]-3-chloropropan-1-one 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>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-Amino-5-hydroxy-2,7-naphthalenedisulfonic acid (4-AHNDS) is a hydroxyl group and nitrogen containing molecule. It is a reactive compound that can be used to extract anions from water. 4-AHNDS has been shown to react with sodium ions in the presence of water, forming a salt that is soluble in water. This chemical also reacts with organic molecules and forms stable complexes. The reaction mechanism of 4-AHNDS has been studied by kinetic analysis and surface methodology measurements.</p>

<p>1-Hydroxycyclopentane-1-carbonitrile is a monomer that is hydrolyzed to form benzoin and cyanohydrins. It can be used in the production of scifinder as a monomer or dimerizer.</p>

<p>Organic intermediate</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-4-nitropyridine is a pyridine compound that has been identified as an environmental contaminant. It is used to synthesize other compounds, such as 4-(3-bromopyridin-2-yl)morpholine, which is used in the synthesis of acetonitrile. 3-Bromo-4-nitropyridine undergoes nucleophilic substitution reactions with amines, leading to homoconjugation and bond cleavage. This reaction may be followed by nitration to give 3-(3'-nitro)pyridine. 3-Bromo-4-nitropyridine can be converted into its n-oxide form or into the ionic form by treatment with acetonitrile.</p>

<p>4-(Benzyloxy)piperidine HCl is a versatile building block that is used in the synthesis of complex compounds such as research chemicals, reagents and speciality chemicals. 4-(Benzyloxy)piperidine HCl is also a useful intermediate in organic synthesis and can be used as a reaction component. 4-(Benzyloxy)piperidine HCl has CAS number 81151-68-0 and is a useful scaffold for chemical syntheses.</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>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>6-Chloro-2-fluoropurine is an analytical reagent with a monoclonal antibody that binds to the nucleic acid of HL-60 cells and can be used for optical analysis. 6-Chloro-2-fluoropurine has been shown to have significant cytotoxicity against HL-60 cells, which may be due to its ability to bind to intracellular targets. 6-Chloro-2-fluoropurine has also been shown to inhibit the growth of HL-60 cells in a fluorescein angiography study and is used as a diagnostic agent for diagnosis of cancer.</p>

Chlorbutanol hemihydrate is an antimicrobial agent that is used as an intra-articular injection, and has been shown to be effective against choline chloride. Chlorbutanol hemihydrate binds to the active substances and reacts with chlorine atom to form an active substance. The reaction rate of chlorbutanol hemihydrate with chlorine atoms is slow, so it can be administered intravenously or intramuscularly. Functional assays have shown that chlorbutanol hemihydrate can inhibit the growth of cancer cells in a dose-dependent manner. It also inhibits the production of oxytocin receptor in mice tissues. Chlorbutanol hemihydrate has been shown to be safe for humans when given at doses up to 10 times higher than the recommended dosage, but may cause allergic reactions in some people.

<p>Versatile small molecule scaffold</p>

<p>Pyrimidine nucleobase; component of nucleic acids</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>Please enquire for more information about (3S)-3- [4- [(2-Chlorophenyl) methyl] phenoxy] tetrahydrofuran 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>2-Bromo-4-iodoanisole is an electrophilic intermediate that can be synthetically prepared by regioselective halogenations of 4-iodoanisole. It is also a substrate for sequential halogenations with bromine or iodine. The 2-bromo-4-iodoanisole reacts with aluminum to form an aluminate, which can be used as a catalyst in organic synthesis. 2-Bromo-4-iodoanisole has been shown to react with aromatic rings by electrophilically attacking the ring and adding a second bromine atom to the ring, leading to quenching of the molecule and formation of structurally diverse products.</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>Ferrocenylmethyl methacrylate is a reactive, irreversible oxidation agent. It is used in the synthesis of hydroxylated polymers and redox-active biological sensors. Ferrocenylmethyl methacrylate has been used as a component in polymerization reactions to produce polymers with recording potential. It has also been used for the detection of cancer cells and for the diagnosis of prostate cancer.</p>

<p>4-Bromo-2,5-dimethoxybenzaldehyde is a nucleophilic compound that can act as an iminium. It is used in the synthesis of chalcones, which are aromatic compounds that have been found to have anticancer properties. 4-Bromo-2,5-dimethoxybenzaldehyde has two isomers: 2,4-dimethoxybenzaldehyde and 2,5-dimethoxybenzaldehyde. The separation of these compounds can be achieved using chromatography with a silica gel column. This process can be done on both the mixture of the two isomers or on one specific isomer. The synthetic pathway for this product begins with benzylpiperazine and piperazine. These two molecules react to form 3,4-dichlorobenzylpiperazine, which reacts with dimethoxybenzyl chloride to form 4-bromo-2,5-dim</p>

<p>2,4,6-Trichloropyrimidine is an antimicrobial agent that belongs to the chemical class of pyrimidine compounds. It inhibits bacterial growth by cross-linking with amino acids and nucleic acids in the cell wall, thereby inhibiting protein synthesis. 2,4,6-Trichloropyrimidine is also a cross-linking agent for polymers such as polyurethane and vinyl chloride. This compound has been shown to be effective against P. aeruginosa and other bacteria that are resistant to antibiotics. 2,4,6-Trichloropyrimidine reacts with water vapor or oxygen nucleophiles to form hydrogen chloride and amine groups. These reactions can be used for identification of this compound in the laboratory.</p>

<p>Please enquire for more information about Tert-butyl N-(8-bromooctyl)carbamate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1,2,3,4-Tetrahydropyridin-4-one is an organic compound that can be synthesized by a cross-coupling reaction between a pyridine and chloroformate. The reaction mechanism involves nucleophilic addition of the amine to the electrophile followed by reductive elimination. This process leads to the formation of a tetrahydroquinoline skeleton with stereoselectivity. Tetrahydropyridin-4-one can also be synthesized from an iminium ion or an activated pyridinium salt. The resulting product will have a different skeleton because it was synthesized through different mechanisms.</p>

<p>Please enquire for more information about Chlorpheniramine N-oxide 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 RC-3095 trifluoroacetate 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>