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(61,055 products)
Found 199650 products of "Building Blocks"
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2-Thiohydantoin
CAS:2-Thiohydantoin is an organic compound that has been structurally characterized. The molecule is planar with a shape that can be described as a chair with both arms. It has been shown to have some interesting biological properties, including the ability to inhibit bowel disease and cancerous growths. 2-Thiohydantoin was also found to be an effective inhibitor of the mitochondrial membrane potential in rats and mice, suggesting it may work by inhibiting mitochondria. 2-Thiohydantoin has also been shown to increase the formation of hydrogen fluoride and other reactive oxygen species, which may contribute to its anti-bacterial activity.Formula:C3H4N2OSPurity:(%) Min. 98%Color and Shape:PowderMolecular weight:116.14 g/mol3-(Trifluoromethyl)phenylacetone
CAS:<p>3-(Trifluoromethyl)phenylacetone is a chiral iminium-type organocatalyst that is used in asymmetric organic reactions. This compound has been shown to be effective for the synthesis of chiral amines and hydroxyl groups, as well as biotransformations. 3-(Trifluoromethyl)phenylacetone binds to substrates through hydrogen bonding, steric interactions, and electrostatic interactions. It also has a high affinity for hydroxides and isosteres. 3-(Trifluoromethyl)phenylacetone can be used as an alternative to L-proline in certain biotransformations because it binds more tightly to the enzyme than L-proline does.</p>Formula:C10H9F3OPurity:Min. 95%Color and Shape:Clear LiquidMolecular weight:202.17 g/mol2-Methoxy-4-propylcyclohexan-1-ol
CAS:<p>2-Methoxy-4-propylcyclohexan-1-ol is a versatile compound with various applications. It is commonly used as an anesthetic and can be found in research chemicals. This compound has been shown to have colloidal properties, making it suitable for use in the formulation of various products. Additionally, 2-Methoxy-4-propylcyclohexan-1-ol has been studied for its potential therapeutic effects on conditions such as casein-related disorders and fatty acid metabolism. Its unique structure allows it to interact with different biological pathways, including protein kinase signaling and carotenoid synthesis. Overall, this compound offers a wide range of possibilities for scientific research and product development.</p>Formula:C10H20O2Purity:Min. 95%Color and Shape:Clear LiquidMolecular weight:172.26 g/molKojic acid dipalmitate
CAS:<p>Tyrosinase inhibitor; skin whitener</p>Formula:C38H66O6Purity:(Hplc) Min. 98.5%Color and Shape:White Off-White PowderMolecular weight:618.93 g/mol4-Methylmorpholine N-oxide monohydrate
CAS:<p>Intermediate for organic syntheses</p>Formula:C5H13NO3Color and Shape:PowderMolecular weight:135.16 g/molO-Methyl-D-threonine
CAS:O-Methyl-D-threonine is an amino acid that is biosynthesized from O-methylserine and D-threonine. It belongs to the class of β-lactam antibiotics and inhibits peptidoglycan synthesis by binding to the catalytic site of the enzyme synthase, which is required for the formation of β-lactam rings in peptidoglycan. The crystal structure of O-methylserine has been determined and analyzed. Mutations in the catalytic tripeptide have been shown to affect its activity, as well as protonation state and carboxylate groups.Formula:C5H11NO3Purity:Min. 98 Area-%Color and Shape:White Off-White PowderMolecular weight:133.15 g/mol1-Phenyl-3-(propan-2-yl)urea
CAS:<p>1-Phenyl-3-(propan-2-yl)urea is a chemical compound that is used in the synthesis of organic compounds. It has been shown to be useful as a building block and also has applications in the preparation of complex compounds. 1-Phenyl-3-(propan-2-yl)urea can be used as a reagent for reactions involving esterification, hydrolysis, cyclization, and nitration. The compound is also useful for research purposes and can be used as an intermediate for other chemicals.</p>Formula:C10H14N2OPurity:Min. 95%Color and Shape:PowderMolecular weight:178.23 g/mol7-Methylindole technical grade
CAS:7-Methylidole is a heterocyclic chemical compound that is used as a precursor in the synthesis of many pharmaceuticals. It has been shown to have an inhibitory effect on the growth of cancer cells in tissue cultures and can be used as a marker for cancer cells. 7-Methylidole is also a virulence factor, which can be seen through assays on bacterial strains. This compound has been proven to be reactive with Polygonum cuspidatum. The reaction produces indirubin, which is a red pigment that is found in some species of Polygonum and other plants.Formula:C9H9NPurity:Min. 95%Color and Shape:PowderMolecular weight:131.17 g/mol5-Methanesulfinylpentanenitrile
CAS:<p>5-Methanesulfinylpentanenitrile is a compound that is found in plants such as broccoli, cabbage, and cauliflower. It has been shown to have anticarcinogenic properties in cell culture studies. The activity of sulforaphane can be increased by the presence of glucosinolates. Sulforaphane inhibits the synthesis of fatty acids and is metabolized by detoxification enzymes. Amides are formed from sulforaphane, which can be detected using preparative high performance liquid chromatography (prep-HPLC). The water solubility of sulforaphane can be increased by heating it to a temperature above its boiling point so that it becomes supercritical (above its critical temperature). This allows for the preparation of dry weight samples for analysis.</p>Formula:C6H11NOSPurity:Min. 95%Molecular weight:145.23 g/molN-Methyl-1-quinolin-2-ylmethanamine dihydrochloride
CAS:<p>Please enquire for more information about N-Methyl-1-quinolin-2-ylmethanamine dihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C11H12N2•(HCl)2Purity:Min. 95%Color and Shape:PowderMolecular weight:245.15 g/mol2-Methoxy-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazole-5-carbaldehyde
<p>Please enquire for more information about 2-Methoxy-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazole-5-carbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C11H20N2O3SiPurity:Min. 95%Color and Shape:PowderMolecular weight:256.37 g/mol(3-Isopropyl-[1,2,4]oxadiazol-5-yl)-acetonitrile
CAS:<p>Heterocycle with nitrile functional handle</p>Formula:C7H9N3OPurity:Min. 95%Color and Shape:PowderMolecular weight:151.17 g/molN-Methyl-N-[1H-indol-3-yl)methyl]amine
CAS:<p>N-Methyl-N-[1H-indol-3-yl)methyl]amine is a plant alkaloid that is found in many plants. It has been shown to have a high constant and to be able to be extracted from the gramine. N-Methyl-N-[1H-indol-3-yl)methyl]amine has been shown to inhibit nitrification and may have potential use as an herbicide. The reaction products of this compound are unknown, but it has been shown to inhibit biosynthesis in vitro assays. This compound also has properties that make it useful for the study of gender and dry weight expression in plants, as well as its ability to be produced by polyclonal antibodies.</p>Formula:C10H12N2Purity:Min. 95%Color and Shape:PowderMolecular weight:160.22 g/mol3,3-Difluorocyclobutanone
CAS:<p>Versatile small molecule scaffold</p>Formula:C4H4F2OPurity:Min. 95%Color and Shape:Clear LiquidMolecular weight:106.07 g/molMono(2-ethylhexyl) terephthalate
CAS:<p>Please enquire for more information about Mono(2-ethylhexyl) terephthalate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C16H22O4Purity:Min. 95%Color and Shape:PowderMolecular weight:278.34 g/mol2-Amino-6-bromo-4-fluorophenol
CAS:<p>2-Amino-6-bromo-4-fluorophenol is a reagent that is used in the synthesis of complex compounds. It is also a useful intermediate for the production of fine chemicals and speciality chemicals. This chemical is used as a building block in the synthesis of versatile building blocks, which are needed to produce speciality chemicals such as pharmaceuticals, agrochemicals, fragrances, and dyes. 2-Amino-6-bromo-4-fluorophenol has been used as a reaction component in the synthesis of various organic compounds. It can be synthesized from phenol or aniline via reductive amination.</p>Formula:C6H5BrFNOPurity:Min. 95 Area-%Color and Shape:PowderMolecular weight:206.01 g/mol2-Methylcinnamic acid, predominantly trans
CAS:<p>The 2-methylcinnamic acid is a derivative of cinnamic acid. It is an organic compound that is a colorless liquid at room temperature. The 2-methylcinnamic acid can be synthesized via the Suzuki coupling reaction between 2-chlorocinnamic acid and 4-hydroxycinnamic acid in the presence of a ruthenium complex, a diphosphine ligand, and an acidic co-solvent. This organic compound has been shown to inhibit prostaglandin synthesis by interacting with the prostanoid receptor, a protein located on the surface of cells that binds to inflammatory agents or hormones. These interactions may also lead to the inhibition of cyclooxygenase (COX) enzymes, which are responsible for prostaglandin synthesis. The 2-methylcinnamic acid can also be converted into flavonoids such as quercetin and apigenin through oxidation reactions.</p>Formula:C10H10O2Purity:Min. 95%Color and Shape:PowderMolecular weight:162.19 g/mol4-Methoxybenzenediazonium tetrafluoroborate
CAS:<p>4-Methoxybenzenediazonium tetrafluoroborate (MBD) is a synthetic molecule that can be prepared by the reaction of sodium hydrogen with UV irradiation. MBD has been shown to have a pharmacokinetic profile similar to methyl cinnamate and is used in the treatment of hyperpigmentation, such as melasma and post-inflammatory hyperpigmentation. MBD interacts with the amino acid tyrosine at its 4-hydroxyl group, cleaving the C-O bond and forming an intramolecular hydrogen bond with the oxygen atom. This results in the formation of diazonium salt which reacts with tyrosinase and inhibits its activity.</p>Formula:C7H7BF4N2OPurity:Min. 98 Area-%Color and Shape:PowderMolecular weight:221.95 g/mol2-Methyl-1,3-propanediol
CAS:<p>2-Methyl-1,3-propanediol is a glycol ether that is used in sample preparation for chemical analysis. It is an antimicrobial agent that has been shown to be active against bacteria such as Escherichia coli and Staphylococcus aureus. 2-Methyl-1,3-propanediol has also been shown to have the ability to inhibit the growth of epidermal cells. This chemical has been shown to be effective in treating skin lesions caused by dermatophytes, fungi and bacterial infections. 2-Methyl-1,3-propanediol inhibits the synthesis of glycol esters, fatty acids and epidermal growth factor through competition with hydroxyl groups on cell membranes. It also chelates metal ions such as Cu2+, Zn2+, Cd2+ and Pb2+.</p>Formula:C4H10O2Purity:Min. 95%Color and Shape:Colorless PowderMolecular weight:90.12 g/mol3-Methoxyacetophenone
CAS:<p>3-Methoxyacetophenone is a bacterial metabolite that is produced by the metabolism of caproic acid. 3-Methoxyacetophenone has been shown to possess antibacterial activity against gram-positive bacteria and to inhibit protein synthesis in these bacteria. The compound class of 3-methoxyacetophenone includes methyl ketones, which are a type of organic compounds containing a carbonyl group (C=O). This compound can be found in bacterial strains such as Pseudomonas aeruginosa and Streptococcus pneumoniae. These bacteria produce 3-methoxyacetophenone during growth on l-tartaric acid or hydrogen tartrate as the sole carbon sources. The organism’s DNA sequences have been determined by deuterium isotope sequencing and l-tartaric acid as the sole carbon source.</p>Formula:C9H10O2Purity:Min. 95%Color and Shape:Colorless Clear LiquidMolecular weight:150.17 g/mol
