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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2-(1-Phenylcyclopropyl)propan-2-amine
CAS:<p>2-(1-Phenylcyclopropyl)propan-2-amine is a versatile building block with a wide range of applications. It can be used as an intermediate for the synthesis of various chemical compounds, as well as a research chemical in laboratories. 2-(1-Phenylcyclopropyl)propan-2-amine is also known to possess high purity and quality, and is an excellent reagent for use in many reactions.</p>Formula:C12H17NPurity:Min. 95%Color and Shape:Clear LiquidMolecular weight:175.27 g/mol4-dibenzocyclooctynol
CAS:<p>4-Dibenzocyclooctynol (4DC) is a synthetic compound that has been shown to be an efficient crosslinker for proteins. It is a ring-opening polymerization agent that reacts with amines and thiols, which are chemical groups found on the side chains of amino acids in proteins. 4DC has been used for the histological analysis of cells, and it has also been used as a pharmacological treatment for Parkinson's disease. 4DC can bind to dopamine receptors, stabilizing them and preventing the degeneration of neurons in the brain. This drug also has potential applications in medical research as a tool for studying glycoconjugates and molecular modeling.</p>Formula:C16H12OPurity:Min. 95%Color and Shape:PowderMolecular weight:220.27 g/mol5-Azetidin-3-yl-3-methyl-[1,2,4]oxadiazole hydrochloride
CAS:<p>5-Azetidin-3-yl-3-methyl-[1,2,4]oxadiazole hydrochloride is a solid that is used as a reagent in the preparation of other chemicals. This chemical has been shown to be useful in the synthesis of complex compounds, such as pharmaceuticals and pesticides.</p>Formula:C6H9N3O•HClPurity:Min. 95%Color and Shape:PowderMolecular weight:175.62 g/mol1-[4-(2-Methoxyethyl)phenoxy]propan-2-one
CAS:<p>1-[4-(2-Methoxyethyl)phenoxy]propan-2-one is a useful scaffold for organic synthesis. It is a versatile building block that can be used as an intermediate in the synthesis of complex compounds with pharmaceutical, agrochemical and other applications.1-[4-(2-Methoxyethyl)phenoxy]propan-2-one is also a reagent in chemical reactions, and has been used to synthesize other compounds such as 1-[4-(2-Methoxyethyl)phenoxy]propan-2-ol (CAS No. 1155083-54-7). This compound has been shown to have good reactivity and high quality, making it an excellent research chemical.</p>Formula:C12H16O3Purity:Min. 95%Molecular weight:208.25 g/mol(2S,3S)-3-Aminobutan-2-ol hydrochloride
CAS:<p>(2S,3S)-3-Aminobutan-2-ol hydrochloride is a high quality chemical that is used as a reagent, intermediate in the production of fine chemicals, and building block for synthesis of other compounds. It is also an important building block in the preparation of speciality chemicals. This compound can be used as an intermediate for the synthesis of various pharmaceuticals, pesticides, dyes, and flavors. (2S,3S)-3-Aminobutan-2-ol hydrochloride can be used in research to prepare new compounds with different properties. It is also a versatile building block that can be used to synthesize many different types of products.</p>Formula:C4H12ClNOPurity:Min. 95%Color and Shape:Clear LiquidMolecular weight:125.6 g/mol3,4,5-Trihydroxybenzamide
CAS:<p>3,4,5-Trihydroxybenzamide (THB) is an active agent that inhibits the synthesis of prostaglandin J2. It has been shown to inhibit the uptake of fatty acids in rat liver cells by blocking fatty acid binding proteins. THB has also been shown to inhibit the chemical structures of nitro and epidermal growth factor. 3,4,5-Trihydroxybenzamide can be used as a cancer treatment by inhibiting the growth and spread of cancer cells. This drug is also believed to have a protective effect on the skin by reducing inflammation and increasing cell proliferation.<br>THB is currently being researched for its ability to suppress histone proteins and growth factors such as HGF or EGF in human HL60 cells.</p>Formula:C7H7NO4Purity:Min. 98 Area-%Color and Shape:Off-White PowderMolecular weight:169.13 g/mol3,4,5-Trimethoxycinnamic acid
CAS:<p>3,4,5-Trimethoxycinnamic acid (TMC) is a hydroxycinnamic acid that is an intermediate in the synthesis of protocatechuic acid. TMC has been found to have an inhibitory effect on the matrix metalloproteinase activity in the cerebellar granule cells and may be useful for treating allergic reactions. It also has anti-inflammatory properties and can be used as a replacement for sodium carbonate in certain industrial processes. TMC also has been shown to have GABA-ergic effects, increasing locomotor activity and reducing anxiety. TMC can also be used as a Chinese herb for the treatment of ganoderma lucidum.</p>Formula:C12H14O5Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:238.24 g/mol2,4,6-Trihydroxybenzoic acid methyl ester
CAS:<p>2,4,6-Trihydroxybenzoic acid methyl ester is a synthetic compound that has been used in animal studies to investigate the inflammatory effects of substances. It has been shown to have anti-inflammatory properties in vitro and in vivo. Furthermore, 2,4,6-Trihydroxybenzoic acid methyl ester has been shown to inhibit the production of tumour necrosis factor-α (TNF-α) and other cytokines. This drug also has anti-fungal activity against Candida albicans and Aspergillus fumigatus. 2,4,6-Trihydroxybenzoic acid methyl ester is biodegradable.</p>Formula:C8H8O5Purity:Min. 95%Color and Shape:PowderMolecular weight:184.15 g/mol2,4,5-Trimethylbenzaldehyde
CAS:<p>2,4,5-Trimethylbenzaldehyde is a cell line that can be used to study the oxidation of α-pinene. It is a chemical compound that belongs to the group of aromatic compounds and has been shown to have high cytotoxicity. It has been found to oxidize other molecules in the body with an electron acceptor such as oxygen or another molecule. 2,4,5-Trimethylbenzaldehyde has also been shown to have biological properties. This product is being researched for its ability to inhibit fatty acid synthesis and reduce cholesterol production in the liver.</p>Formula:C10H12OPurity:Min. 95%Molecular weight:148.2 g/mol2,4,5-Trimethoxybenzaldehyde
CAS:<p>2,4,5-Trimethoxybenzaldehyde is a natural compound that belongs to the group of sephadex g-100. It is used as an absorbent and has been shown to react with human immunoglobulin in the presence of tiglic acid. The reaction mechanism for this chemical is not well understood but it is believed that intermolecular hydrogen bonding may be occurring. 2,4,5-Trimethoxybenzaldehyde has been shown to have anti-inflammatory effects when tested on rats in a laboratory setting. This chemical has also been used as an analytical reagent for biological samples and biological studies as well as a preparative hplc column. Optical sensors have also been used to detect this chemical in various types of optical sensing experiments. X-ray crystal structures have also been obtained for this compound using synchrotron radiation.</p>Formula:C10H12O4Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:196.2 g/mol2,3,4-Trimethoxybenzoic acid
CAS:<p>2,3,4-Trimethoxybenzoic acid is a molecule that has been shown to stimulate epidermal growth. It is a methylating agent that can be used to produce 2-hydroxybenzoic acid from protocatechuic acid. The hydroxy group on the 2,3,4-trimethoxybenzoic acid binds to the chloride ion in the protocatechuic acid and removes it from the molecule. This reaction mechanism is supported by x-ray crystal structures of protocatechuic acid and 2,3,4-trimethoxybenzoic acid.</p>Formula:C10H12O5Purity:Min. 95%Color and Shape:PowderMolecular weight:212.2 g/mol2,3,4-Trimethoxy-6-methylbenzaldehyde
CAS:<p>2,3,4-Trimethoxy-6-methylbenzaldehyde is a synthetic coumarin with antibacterial activity. It is synthesized by the condensation of 3-hydroxyacetophenone and benzaldehyde. 2,3,4-Trimethoxy-6-methylbenzaldehyde has been shown to have antibacterial activity against both Gram-positive and Gram-negative bacteria. This molecule has also been shown to inhibit the growth of Gram negative bacteria in the presence of hydrogen peroxide. The crystal structure of this molecule was determined by XRD analysis and shows that it contains a dihedral angle of about 155°.</p>Formula:C11H14O4Purity:Min. 95%Molecular weight:210.23 g/mol2,4,6-Trimethylbenzoic acid
CAS:<p>2,4,6-Trimethylbenzoic acid is a molecule that belongs to the class of carboxylates. It has been shown to exhibit anticarcinogenic properties in patients with cervical cancer. 2,4,6-Trimethylbenzoic acid inhibits the growth of cervical cancer cells by blocking the activation of ferrocenecarboxylic acid (FCCA). This compound also blocks the activity of hydrogen bond and nitrogen atoms that are essential for cell division and development. 2,4,6-Trimethylbenzoic acid is used as an intermediate in the production of ferrocene derivatives. It can be used for acylation reactions with aromatic or aliphatic amines under acidic conditions.</p>Formula:C10H12O2Purity:Min. 95%Color and Shape:PowderMolecular weight:164.2 g/mol2,4,6-Trimethoxybenzonitrile
CAS:<p>2,4,6-Trimethoxybenzonitrile is a ligand that forms coordination complexes with metal ions. It can be used to make N-oxide compounds and reaction products with aryl chlorides. The 2,4,6-trimethoxybenzonitrile ligand has been shown to form cross-coupling complexes with benzotriazolyl. This compound is soluble in organic solvents and has a vapor pressure of 0.0025 mm Hg at 25°C. The molecular weight of this compound is 196.2 g/mol and its melting point is 190°C. 2,4,6-Trimethoxybenzonitrile has a symmetric molecule in the gas phase and an asymmetric molecule in solution due to the interactions of hydrogen bonding and van der Waals forces.</p>Formula:C10H11NO3Purity:Min. 95%Color and Shape:PowderMolecular weight:193.2 g/mol2,4,6-Trihydroxybenzophenone
CAS:<p>2,4,6-Trihydroxybenzophenone is a phenolic compound that has been shown to have significant inhibitory activities against the growth of bacteria in vitro. It can be used as a preservative for oils and fats. This product also inhibits the benzoate degradation pathway in E. coli and inhibits the synthesis of phenylpropanoids by inhibiting the activity of phenylalanine ammonia-lyase (PAL). 2,4,6-Trihydroxybenzophenone also has an inhibitory effect on cell proliferation and induces apoptosis in human leukemia cells. 2,4,6-Trihydroxybenzophenone belongs to the group of compounds called hypericins (hyperforin) that are produced by Hypericum perforatum plants. The biosynthesis of this molecule is thought to involve two consecutive hydroxylations at positions 4 and 6 on the aromatic ring.</p>Formula:C13H10O4Purity:Min. 95%Color and Shape:Off-White PowderMolecular weight:230.22 g/mol2,4,6-Trichlorobenzonitrile
CAS:<p>2,4,6-Trichlorobenzonitrile is a chlorine-containing chemical that has been used as a pesticide. It is a highly toxic substance and can be fatal if ingested. 2,4,6-Trichlorobenzonitrile is converted to chloride in soil and water by microbial action. This chemical can be activated by light or temperature changes and is used in the production of pesticides that are phytotoxic. It also has been shown to have thermodynamic properties that allow it to act as an environmental pollutant. 2,4,6-Trichlorobenzonitrile can react with sulfoxides to form chloromethylation products such as 2,3,5-trichloroethanol. These reactions are catalyzed by metal ions such as Fe(II) and Mn(II).</p>Formula:C7H2Cl3NPurity:Min. 95%Color and Shape:PowderMolecular weight:206.46 g/mol3,4,5-Tribromobenzoic acid
CAS:<p>3,4,5-Tribromobenzoic acid is a metabolite of 3-indoleacetic acid. It is excreted in the urine and has a phaseolus-like physiological activity. This compound has been found to reduce the number of internodes in plants and increase the number of subjacent nodes. In addition, it has been shown to inhibit abscission (the separation of plant parts) by inhibiting the release of auxin from the upper node. The structural properties of 3,4,5-tribromobenzoic acid are similar to those of benzoic acid and it can be found naturally in some plants. Diversity in this chemical has been found among different species: for example, 2,3,5-triiodobenzoic acid is only present in citrus fruits such as oranges and lemons.</p>Formula:C7H3Br3O2Purity:Min. 95%Color and Shape:PowderMolecular weight:358.81 g/mol3,4,5-Trimethoxyacetophenone
CAS:<p>3,4,5-Trimethoxyacetophenone is a natural product that has been shown to be an antimycotic. It has significant cytotoxicity against A549 cells and also inhibits the growth of cancer cells in culture. 3,4,5-Trimethoxyacetophenone has a low bioavailability due to its chemical properties and inhibitory effects on CYP3A4. This compound is metabolized by the liver into metabolites with inhibitory properties. 3,4,5-Trimethoxyacetophenone also binds to methoxy groups on proteins.</p>Formula:C11H14O4Purity:Min. 99 Area-%Color and Shape:White PowderMolecular weight:210.23 g/mol3,4,5-Tribromoacetophenone
CAS:<p>3,4,5-Tribromoacetophenone is a high quality and versatile chemical with many special applications. It is an important intermediate for the production of various chemicals, such as plastics and pharmaceuticals. This compound can be used as a starting material for the synthesis of more complex compounds by reacting with other chemicals. 3,4,5-Tribromoacetophenone also has a number of useful properties that make it ideal for research purposes.</p>Formula:C8H5Br3OPurity:Min. 95%Color and Shape:PowderMolecular weight:356.84 g/mol2,4,6-Trimethoxybenzoic acid
CAS:<p>2,4,6-Trimethoxybenzoic acid (TMB) is a monomer that belongs to the class of organic compounds known as phenols. It can undergo dehydrogenation reactions with nitroethane in the presence of trifluoroacetic acid and catalytic amounts of hydrogen gas. TMB has been shown to interact with an allyl group in other molecules. The reaction system was studied under different flow rates and was found to be best described by an isotherm equation.</p>Formula:C10H12O5Purity:Min. 95%Color and Shape:PowderMolecular weight:212.2 g/mol
