Building Blocks
This section contains fundamental products for the synthesis of organic and biological compounds. Building blocks are the essential starting materials used to construct complex molecules through various chemical reactions. They play a critical role in drug discovery, material science, and chemical research. At CymitQuimica, we offer a diverse range of high-quality building blocks to support your innovative research and industrial projects, ensuring you have the essential components for successful synthesis.
Subcategories of "Building Blocks"
- Boronic Acids & Boronic Acid Derivatives(5,756 products)
- Chiral Building Blocks(1,242 products)
- Hydrocarbon Building Blocks(6,093 products)
- Organic Building Blocks(60,519 products)
Found 195533 products of "Building Blocks"
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1,2-Bis(diphenylphosphino)ethane
CAS:<p>1,2-Bis(diphenylphosphino)ethane is a ligand that binds to the metal molybdenum. It has been shown to have biochemical properties in relation to its ability to form complexes with adriamycin and other drugs. The redox potential of 1,2-Bis(diphenylphosphino)ethane depends on the presence of sodium ions. This ligand is able to bind to the iron in the mitochondrial membrane and can affect the mitochondrial membrane potential. X-ray crystal structures show that this ligand binds to a monosodium salt. 1,2-Bis(diphenylphosphino)ethane has been shown to be a potent inhibitor of transfer reactions and is used as an analytical reagent for structural analysis.</p>Formula:C26H24P2Purity:Min. 98 Area-%Color and Shape:White Off-White PowderMolecular weight:398.42 g/mol2-Bromo-1H-imidazole
CAS:<p>2-Bromo-1H-imidazole is an environmental pollutant that has been detected in the atmosphere, water, and soil. It is used as a pesticide and has been found to be an impurity in biphenyl. 2-Bromo-1H-imidazole can be used as a substrate for the Suzuki coupling reaction or as a starting material for the synthesis of imidazole derivatives. The compound spontaneously fragments under acidic conditions to form nitric acid and hydrogen bromide. 2-Bromo-1H-imidazole has been shown to inhibit hepatitis C virus (HCV) replication and induce cancer cell apoptosis in vitro.<br>2-Bromo-1H-imidazole is also known to cause DNA fragmentation in cells through oxidation by reactive oxygen species or through spontaneous decomposition of the molecule into acid, bromine radicals, and ammonia.</p>Formula:C3H3BrN2Purity:Min. 95%Color and Shape:PowderMolecular weight:146.97 g/mol3-Bromo-5-cyanobenzoic acid
CAS:<p>3-Bromo-5-cyanobenzoic acid is a fine chemical that is used as a reagent or intermediate in the production of other chemicals. 3-Bromo-5-cyanobenzoic acid can be used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and perfumes. This compound is also useful as a building block for making speciality chemicals and research chemicals. 3-Bromo-5-cyanobenzoic acid is versatile because it can be used in many different reactions with many different substrates to make many different products.</p>Formula:C8H4BrNO2Purity:Min. 95%Color and Shape:PowderMolecular weight:226.03 g/molN-Boc-2-methyl-L-proline
CAS:<p>N-Boc-2-methyl-L-proline is a chemical compound that is used as a building block in the synthesis of other compounds. This substance is also an intermediate in the production of pharmaceuticals and pesticides. The compound has been shown to have high quality, versatility, and complexity. N-Boc-2-methyl-L-proline can be used as a reagent for research or as a speciality chemical. The CAS number for this substance is 103336-06-7.</p>Formula:C11H19NO4Purity:Min. 95%Color and Shape:White To Off-White SolidMolecular weight:229.27 g/mol2,2'-Bipyridine-6,6'-(1H,1'H)dione
CAS:<p>2,2'-Bipyridine-6,6'-(1H,1'H)dione is a high-quality compound that is used as a reagent to provide a variety of useful compounds. This compound can be used as a building block for various chemical syntheses or as a component in many reactions. It is also a versatile building block and can be used in the synthesis of other compounds. 2,2'-Bipyridine-6,6'-(1H,1'H)dione has been shown to be an effective intermediate for organic synthesis.</p>Formula:C10H8N2O2Purity:Min. 95%Color and Shape:Off-White To Light Brown SolidMolecular weight:188.18 g/mol4-Bromo-3-chlorobenzoic acid
CAS:<p>4-Bromo-3-chlorobenzoic acid is a molecule that belongs to the class of antimicrobial compounds and is used for the treatment of gram-negative pathogens. It inhibits the growth of these bacteria by blocking their ability to synthesize DNA, RNA, and proteins. 4-Bromo-3-chlorobenzoic acid has been shown to be effective against bacteria in mammalian cells and also has activity against multidrug resistant strains. This compound is biosynthesized in plant cells from carbon sources like glucose, and it can be found in plants like carrot tissue. The resistance of bacteria to this compound has been observed globally, with outbreaks occurring in Japan and India.</p>Formula:C7H4BrClO2Purity:Min. 95%Color and Shape:White PowderMolecular weight:235.46 g/mol3-Bromobenzylamine
CAS:<p>3-Bromobenzylamine is a chemical compound that belongs to the class of amines. It is used as an intermediate in organic synthesis, and its derivative 3-bromobenzylamine hydrochloride is used in pharmaceuticals as a heart stimulant. 3-Bromobenzylamine can be synthesized by reacting an amine with phosgene and then brominating it. This chemical has been shown to have inhibitory activity against cancer cells and can be used for the treatment of cancer. 3-Bromobenzylamine has also been shown to inhibit the growth of bacteria, fungi, and viruses in vitro. 3-Bromobenzylamine may also be useful for treating psoriasis due to its ability to inhibit prostaglandin synthesis.</p>Formula:C7H8BrNPurity:Min. 95%Color and Shape:Colorless PowderMolecular weight:186.04 g/molFmoc-Ala-Pro-Pro-OH
CAS:<p>Fmoc-Ala-Pro-Pro-OH is an amino acid that belongs to the class of speciality chemicals. It is a versatile building block for organic synthesis, with applications in pharmaceuticals, agrochemicals, and other chemical industries. The CAS number for Fmoc-Ala-Pro-Pro-OH is 386768-25-8.</p>Formula:C28H31N3O6Purity:Min. 95%Color and Shape:PowderMolecular weight:505.56 g/mol3-Fluoro-4-methoxyaniline
CAS:<p>3-Fluoro-4-methoxyaniline is a chemical intermediate. It is an aminopyridine that is used in the synthesis of bosutinib, an anticancer drug. 3-Fluoro-4-methoxyaniline binds to the ATP binding site of the cell's mitochondria and prevents the release of cytochrome c from the mitochondria, which leads to apoptosis. 3-Fluoro-4-methoxyaniline also has antimitotic effects and can inhibit the growth of tumor cells. 3-Fluoro-4-methoxyaniline has been shown to have poor cellular uptake, which may be due to its interaction with positron emission tomography (PET) agents such as cyanuric acid or glycopeptide. This chemical has also been shown to be a good surrogate for chloride ions in studies on transfected tumor cells.</p>Formula:C7H8FNOPurity:Min. 98.5%Color and Shape:Off-White PowderMolecular weight:141.14 g/mol3-[Bis(phenylmethyl)amino]-5-fluoro-6-methyl-2-(phenylmethoxy)benzoic acid phenyl ester
CAS:<p>Building block in tetracycline antibiotic synthesis</p>Formula:C35H30FNO3Purity:Min. 95%Color and Shape:PowderMolecular weight:531.62 g/mol8-Bromo-1-octene
CAS:<p>8-Bromo-1-octene is a biologically active molecule that is an aliphatic hydrocarbon with a hydroxyl group. It is used in the study of growth factors and viruses, and has been shown to inhibit the growth of cells in tissue cultures. 8-Bromo-1-octene has also been shown to inhibit RNA synthesis and protein synthesis in vitro, as well as the growth of recombinant virus. 8-Bromo-1-octene can be synthesized by reacting 6-bromo-1-hexene with hydrogen bromide, or can be obtained from commercially available sources.</p>Formula:C8H15BrPurity:Min. 95%Color and Shape:Colorless Slightly Yellow Clear LiquidMolecular weight:191.11 g/mol2-Bromo-4-chloropyridine
CAS:<p>2-Bromo-4-chloropyridine is a 4-chloropyridine derivative with the chemical structure of a heterocyclic amine. It has been synthesised as an analog of 2,4,6-trimethylaniline to explore its pharmacological effect. 2-Bromo-4-chloropyridine has been shown to have a bladder carcinogenic effect in animals. The compound was evaluated for its potential to cause bladder cancer in humans by determining the concentration of the compound in human urine following oral administration and by measuring the frequency of bladder tumors in rats. It has also been found that 2-bromo-4-chloropyridine inhibits serotonin receptors (5HT2C) and dopamine receptors (D2).</p>Formula:C5H3BrCINPurity:Min. 95%Color and Shape:Off-White To Yellow Solid Or Liquid (May Vary)Molecular weight:192.44 g/mol1-(2-Dimethylaminoethyl)-4-methylpiperazine
CAS:<p>Polyurethane is a polymer that is synthesized by the reaction of diisocyanates with polyols, such as glycols or sugar alcohols. Polyurethanes are used in a wide variety of products, including coatings, foams and elastomers. 1-(2-Dimethylaminoethyl)-4-methylpiperazine (DMP) is an ionic surfactant that is commonly used as an extender and/or viscosity stabilizer in polyurethane systems. DMP provides good wetting properties to the coating and improves film formation, surface smoothness and abrasion resistance. It also helps to reduce the hardness of the surface film, which can be beneficial when using soft materials such as foam or rubber.</p>Formula:C9H21N3Purity:Min. 95%Color and Shape:Clear LiquidMolecular weight:171.28 g/mol5-Bromo-1-pentene
CAS:<p>5-Bromo-1-pentene (5BP) is an antitumoral drug that has potent inhibitory activity against the t-cell leukemia cell line and other tumor cells. 5BP is an organoborane ester with a bromine atom at the 1-position. It is synthesized by reacting trifluoroacetic acid with a hydrohalic acid such as hydrochloric acid, or with a metal halide such as sodium carbonate, followed by reaction with dimethyl formamide and n-dimethylformamide. The 5BP molecule has a coordination geometry of octahedral and its structure consists of three hydrogen atoms, two methyl groups, one hydroxyl group, and one unsaturated alkyl group. The mechanism of action of 5BP is still unclear. The inhibition of protein synthesis may be due to the steric hindrance caused by the bulky bromine atom at the 1 position on the benzene ring.</p>Formula:C5H9BrPurity:Min. 95%Color and Shape:Colorless Clear LiquidMolecular weight:149.03 g/mol3,5-Dimethyl-4-hydroxyphenylacetic acid
CAS:<p>3,5-Dimethyl-4-hydroxyphenylacetic acid (DHPA) is a fine chemical that can be used as a building block in the production of other chemicals. It is a useful intermediate in organic synthesis and has been used to produce pharmaceuticals, fragrances, and dyes. DHPA is also an important reagent for research purposes and can be used to synthesize other compounds.</p>Formula:C10H12O3Purity:Min. 95%Color and Shape:Off-White PowderMolecular weight:180.2 g/mol3,4-Dichloro-2-methylpyridine
CAS:<p>3,4-Dichloro-2-methylpyridine is a novel sulfur analogue that has been shown to have significant antitumor activity in breast cancer xenografts. 3,4-Dichloro-2-methylpyridine inhibits the growth of tumor cells by binding to their DNA and inhibiting RNA synthesis. It also inhibits the production of reactive oxygen species and stabilizes cell membranes. 3,4-Dichloro-2-methylpyridine has been found to be active against human tumors in vivo and is a potential anticancer drug for human use.</p>Formula:C6H5Cl2NPurity:Min. 95%Color and Shape:PowderMolecular weight:162.02 g/mol3,4-Dihydro-2H-pyran-2-methanol
CAS:<p>3,4-Dihydro-2H-pyran-2-methanol is a tetrahydropyran alcohol that has been shown to be able to form cationic polymers in the presence of a ring-opening metathesis polymerization catalyst. The chloride anion is also capable of initiating the polymerization reaction. This compound has potential applications as a drug delivery agent or biomaterials scaffold due to its ability to act as a linker for the synthesis of biocompatible polymers. 3,4-Dihydro-2H-pyran-2-methanol can also be used in molecular modelling studies to explore the reactivity between hydroxy groups and nucleophiles.</p>Formula:C6H10O2Purity:Min. 95%Color and Shape:Colorless PowderMolecular weight:114.14 g/mol2,2'-Bipyridine-4,4'-dicarboxylic acid
CAS:<p>2,2'-Bipyridine-4,4'-dicarboxylic acid (BBDA) is a synthetic molecule that has been used as an oxidant in organic synthesis. It is a redox-active compound with a reversible oxidation potential of +0.2 V. The electron transfer to the adjacent nitrogen atom is accompanied by light emission at 490 nm and chloride ion release. BBDA reacts with potassium dichromate in water to form 2,2'-bipyridine-6,6'-dicarboxylic acid and potassium chloride. This reaction can be monitored by magnetic resonance analysis and X-ray absorption spectroscopy. The formation of BBDA from dimethylformamide and esters has been reported in the literature.</p>Formula:C12H8N2O4Purity:Min. 95%Color and Shape:PowderMolecular weight:244.21 g/molDL-Valine
CAS:<p>Valine is a non-essential, branched-chain amino acid that is used for the treatment of bowel disease. Valine is a water-soluble, colorless and odorless crystalline powder that has a sour taste. It can be prepared by reacting valeric acid with ammonia in the presence of an alkali or by hydrolysis of proteins. Valine is also widely distributed in animal tissues, where it participates in the biosynthesis of important biological compounds such as coenzyme A. The optimum concentration to achieve maximum electrochemical impedance spectroscopy (EIS) signal was observed at 20 mM. The EIS signal was found to be dependent on the pH and protein content of the solution matrix. Valine binds to human serum albumin and exhibits strong hydrogen bonding interactions. In addition, valine possesses a signal peptide that helps export it from cells into blood plasma.</p>Formula:C5H11NO2Color and Shape:PowderMolecular weight:117.15 g/molBenzofuran-2-carboxaldehyde
CAS:<p>Benzofuran-2-carboxaldehyde is a compound that inhibits metathesis reactions. It has been shown to inhibit the growth of cancer cells in vivo and in vitro. Benzofuran-2-carboxaldehyde also shows estrogen receptor modulator activity, which may be due to its ability to bind to estrogen receptors. The molecular modelling study of this compound reveals a possible mechanism for benzofuran-2-carboxaldehyde’s inhibition of metathesis reactions as well as its cytotoxicity. This mechanism suggests that the benzofuran-2-carboxaldehyde molecule can form hydrogen bonds with diphenyl ether and mcf7 cells, leading to their destabilization.</p>Formula:C9H6O2Purity:Min. 95%Molecular weight:146.14 g/mol
