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(6,095 products)
- Organic Building Blocks(61,038 products)
Found 196817 products of "Building Blocks"
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4-Nitroindole
CAS:<p>4-Nitroindole is a versatile building block with a variety of applications. It can be used in the synthesis of complex compounds, research chemicals, and reagents. 4-Nitroindole is also useful in the synthesis of speciality chemicals and as an intermediate for the preparation of other compounds. This compound is high quality and has many uses as a reaction component or scaffold.</p>Formula:C8H6N2O2Molecular weight:162.15 g/molRef: 3D-N-2980
25gTo inquire50gTo inquire100gTo inquire250gTo inquire500gTo inquire-Unit-kgkgTo inquire4-tert-Butylaniline
CAS:<p>4-tert-Butylaniline is a chemical compound with the molecular formula C6H7N. It is an organic base that has acidic properties and can be used as an amine. 4-tert-Butylaniline is used in the manufacture of other chemicals, such as herbicides, pesticides, and pharmaceuticals. 4-tert-Butylaniline binds to metal ions such as palladium by hydrogen bonding. This binding increases the reactivity of the metal ion and allows it to catalyze reactions that would otherwise not occur. 4-tert-Butylaniline also has transport properties and binds to replicon cells through adsorption mechanisms.</p>Formula:C10H15NPurity:Min. 95%Color and Shape:Colorless Clear LiquidMolecular weight:149.23 g/mol2-Bromo-5-iodopyridine
CAS:<p>2-Bromo-5-iodopyridine is a compound that has been studied for its potential use in the treatment of neurodegenerative diseases. It inhibits nicotinic acetylcholine receptors, which are involved in the transmission of nerve impulses to the muscles. 2-Bromo-5-iodopyridine binds to acetylcholine receptors, blocking the uptake of acetylcholine and preventing it from binding with the receptor. This leads to an increase in acetylcholine levels, which increases muscle contraction and improves brain function. The crystal structure of 2-bromo-5-iodopyridine has been determined by x-ray diffraction studies. The molecule contains two bromine atoms and five iodine atoms, which are arranged such that they form a square planar geometry around a central metal ion (hydrochloric acid). Nitrogen atoms are found on opposite corners of this square plane. These nitrogen atoms can be substituted with chloride</p>Formula:C5H3BrINPurity:Min. 95%Color and Shape:Off-White PowderMolecular weight:283.89 g/molL-Glutamic acid monopotassium salt monohydrate
CAS:<p>Amino acid; neurotransmitter; flavor enhancer</p>Formula:C5H8KNO4·H2OColor and Shape:White PowderMolecular weight:203.23 g/molGlycine ethyl ester hydrochloride
CAS:<p>Used with EDC for carboxyl-foot printing studies of proteins</p>Formula:C4H9NO2•HClPurity:Min. 95%Color and Shape:PowderMolecular weight:139.58 g/molGallic acid anhydrous
CAS:<p>Gallic acid anhydrous is a compound that is found in plants and has antioxidant properties. Gallic acid anhydrous can be used as a model system for the study of electrochemical impedance spectroscopy. It has shown to have anti-cancer activity in vitro, but not in vivo, against squamous carcinoma cells. In addition, gallic acid anhydrous has been shown to inhibit oral pathogens and to scavenge anion radicals. Gallic acid anhydrous may have structural similarities to procyanidin B4, which is important for its antioxidant activity.</p>Formula:C7H6O5Purity:Min. 99 Area-%Color and Shape:White PowderMolecular weight:170.12 g/mol4-Vinylpyridine, stabilized with 100ppm Hydroquinone
CAS:<p>4-Vinylpyridine, stabilized with 100ppm Hydroquinone is a chemical compound that belongs to the class of pyridines. It has been shown to be stable in aqueous solution and to have a high water permeability. The reaction mechanism is not known, but it is thought that the quaternization of the vinyl group may be involved. 4-Vinylpyridine has been used as a component for the synthesis of polymers and can also be used in palladium-catalyzed coupling reactions.</p>Formula:C7H7NPurity:Min. 97 Area-%Color and Shape:Colorless Clear LiquidMolecular weight:105.14 g/molH-Gly-Gly-Gly-NH2·HCl
CAS:<p>Glycine is a non-essential amino acid with a pKa of 9.3. It is a building block of proteins and can be used to synthesize polypeptides. Glycine has been shown to function as an antigen in humans and has been used in pharmaceutical preparations and clinical studies as an immunological agent, such as in the treatment of hepatitis B virus infection. Glycine is also a component of protonated glycoconjugates, which are found in human serum. In addition to its role as an important amino acid, glycine is also an important molecule for kinetic studies because it has a high transfer rate between molecules and macrocyclic structures. This transfer rate can be used to study the conjugation reactions that occur with fluorescent compounds, like fluorescein, which can be used for labeling antibodies.</p>Formula:C6H12N4O3·HClPurity:Min. 95%Color and Shape:PowderMolecular weight:224.65 g/molTrans-methylisoeugenol
CAS:<p>Trans-methylisoeugenol is a natural compound that has been shown to have anti-inflammatory, antioxidant, and immunomodulatory properties. It is a metabolite of isoeugenol, which is a constituent of the essential oils from plants such as angelica dahurica and eugenia caryophyllata. Trans-methylisoeugenol binds to the glucuronide conjugate receptor on the cell surface, leading to various effects including inflammatory responses. Trans-methylisoeugenol also inhibits the activity of enzymes such as benzalkonium chloride and eugenol that are responsible for inflammation. Molecular docking analysis predicts that trans-methylisoeugenol may bind to the same site on the receptor as benzalkonium chloride.</p>Formula:C11H14O2Purity:Min. 90 Area-%Color and Shape:PowderMolecular weight:178.23 g/mol4-(4-Fluorophenoxy)benzylamine hydrochloride
CAS:<p>4-(4-Fluorophenoxy)benzylamine hydrochloride is a metabolic agent that inhibits the metabolism of phenylpropionic acid and butanoic acid. It is used industrially as an oxime to protect other organic compounds from damage by peroxides, such as in polymerization reactions. 4-(4-Fluorophenoxy)benzylamine hydrochloride has been shown to be effective in treating metabolic diseases, such as phenylketonuria and urea cycle disorders.</p>Formula:C13H12FNO·HClPurity:Min. 95%Color and Shape:PowderMolecular weight:253.7 g/mol2,3,4,6-Tetra-O-benzyl-D-galactopyranose
CAS:<p>2,3,4,6-Tetra-O-benzyl-D-galactopyranose is an isomeric sugar that is found in a variety of natural and synthetic carbohydrates. It has been shown to inhibit glycosidase enzymes such as aminoglycoside N-acetyltransferases and α-glycosidases. The stereoselective properties of 2,3,4,6-Tetra-O-benzyl-D-galactopyranose make it a good candidate for the treatment of drug resistant bacteria. This compound has been shown to have inhibitory activity against the hydrolase family of enzymes that includes proteases, lipases, and phospholipases.</p>Formula:C34H36O6Purity:Min. 95%Color and Shape:PowderMolecular weight:540.6 g/mol2-Methyl-1-benzofuran-3-carboxylic acid
CAS:<p>2-Methyl-1-benzofuran-3-carboxylic acid is a type of carboxylic acid that is cytotoxic to cancer cells. It is a major metabolite of the anticancer drug 2,4,5-trimethoxybenzaldehyde and has been shown to be effective against human breast cancer cells. The ester hydrochloride salt form of this compound has been shown to be an effective inhibitor of esterase activity in vitro. This inhibition leads to increased accumulation of 2-methyl-1-benzofuran-3-carboxylic acid in tumor tissue, which may be due to its ability to inhibit the synthesis of proteins required for the transport and metabolism of other drugs. The x-ray structure analysis revealed that this compound binds to the active site of beta lactamases in an orientation that overlaps with substrate binding sites. This binding prevents the formation of a covalent bond between penicillin G</p>Formula:C10H8O3Purity:Min. 95%Color and Shape:PowderMolecular weight:176.17 g/molPutrescine dihydrochloride
CAS:<p>Putrescine is a polyamine plant growth regulator affecting the synthesis of macromolecules. Promotes adventitious root formation. Precursor of spermidine.</p>Formula:C4H14Cl2N2Purity:Min. 98.0 Area-%Molecular weight:161.08 g/molRef: 3D-P-8000
1kgTo inquire5kgTo inquire10kgTo inquire25kgTo inquire2500gTo inquire-Unit-kgkgTo inquire3-Methyl-1,2,4-thiadiazole-5-carbohydrazide
CAS:<p>3-Methyl-1,2,4-thiadiazole-5-carbohydrazide is an intermediate in the synthesis of fezolinetant. It can be used as a pharmaceutical intermediate.</p>Formula:C4H6N4OSPurity:Min. 95%Molecular weight:158.18 g/molQuinoline 2,4-dicarboxylic acid
CAS:<p>Quinoline 2,4-dicarboxylic acid (QDA) is a novel cytotoxic agent that targets cervical cancer cells. It inhibits the uptake of glucose and other nutrients by cervical cancer cells, leading to cell death through apoptosis. QDA also inhibits the expression of genes involved in cross-linking reactions, which are important for the structural integrity of proteins. This agent has been shown to inhibit the growth of aniline-induced breast cancer cells and glutamate-stimulated PC12 cells. QDA binds to DNA and forms covalent bonds with nucleotide bases, inhibiting DNA synthesis, as well as interfering with protein synthesis and cell division. The QDA mechanism is similar to that of benzoquinolines and estrone sulfate.</p>Formula:C11H7NO4Purity:Min. 95%Color and Shape:White PowderMolecular weight:217.18 g/mol4-Chlorophenylurea
CAS:<p>4-Chlorophenylurea is an urea derivative that has been shown to inhibit the activity of a number of enzymes. It has been used as a chemical intermediate and in the synthesis of other compounds. 4-Chlorophenylurea is stable in dry environments and does not react with air. The enzyme hydrolysis can be inhibited by adding piperonyl butoxide, which prevents the cleavage of the urea ring. The enzyme's activity can also be suppressed by adding acidic compounds such as hydrochloric acid, which increases its activation energy. The chemical structure of 4-Chlorophenylurea contains a carbonyl group and two chloro groups that are responsible for its inhibitory effect on tumour cells. This compound can also be analysed using liquid chromatography methods, which provide structural data about the product being tested.</p>Formula:C7H7ClN2OPurity:Min. 95%Color and Shape:PowderMolecular weight:170.6 g/mol2,5-Furandicarboxylic diethyl ester
CAS:<p>2,5-Furandicarboxylic acid diethyl ester is a synthetic monomer that can be used in the production of polyesters. It is synthesized from primary alcohols by an acid-catalyzed reaction, followed by dehydration with phosphotungstic acid or heating to produce furanic and furfural. 2,5-Furandicarboxylic acid diethyl ester is a sustainable compound because it does not contain any toxic chemicals and it only contains one carbon atom that can be recycled into biomass. It has been shown to have control experiments and sequences that are similar to diglycerol.</p>Formula:C10H12O5Purity:Min. 95%Color and Shape:PowderMolecular weight:212.2 g/mol2-Quinolinecarboxylic acid
CAS:<p>2-Quinolinecarboxylic acid is an antibiotic that is used in the treatment of bacterial infections and has inhibitory properties. It has been shown to be a competitive inhibitor of the enzyme quinolinate phosphoribosyltransferase, which catalyzes the conversion of quinolinic acid to nicotinic acid. 2-Quinolinecarboxylic acid binds to the active site of the enzyme and prevents substrate binding, thereby blocking the production of nicotinic acid. This drug also inhibits bacterial growth by binding to DNA-dependent RNA polymerase, thereby preventing transcription and replication. The high frequency of human activity has been shown using a patch-clamp technique on human erythrocytes. This active form is metabolized through a number of metabolic transformations, including hydrolysis by esterases or glucuronidases, oxidation by cytochrome P450 enzymes, reduction by glutathione reductase, or conjugation with glucur</p>Formula:C10H7NO2Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:173.17 g/molBetonicine
CAS:<p>Betonicine is a natural compound that has been shown to have therapeutic effects in autoimmune diseases. It has been used as a model system for studying plant physiology and to determine the transport properties of hydroxyl groups. Betonicine has also been shown to have receptor activity, which is responsible for its disease-modifying effects in autoimmune diseases. Betonicine is an inorganic acid that can be synthesized from the reaction between ammonia and nitric acid. It can also be extracted from plants such as cress seeds, which are rich in nitrogen atoms. The titration calorimetry method was used to measure the concentration of betonicine in coli K-12 cells.</p>Formula:C7H13NO3Purity:Min. 95%Color and Shape:PowderMolecular weight:159.18 g/molN-(5-Amino-2,4-difluorophenyl)propane-1-sulfonamide
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H12F2N2O2SPurity:Min. 95%Color and Shape:PowderMolecular weight:250.27 g/mol
