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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4-Methylpyridine-2-thiol
CAS:<p>4-Methylpyridine-2-thiol is a ligand that binds to metal ions. It has been shown to be an effective photoelectron scavenger for mercury and lead, as well as a wide variety of other metals. 4-Methylpyridine-2-thiol is also an important monomer in the preparation of polymers and resins. This ligand has been used in the synthesis of compounds with cyclic structures and hydrochloric acid, as well as being crystallized with x-ray crystallography. The properties of this ligand have been studied by voltammetry, spectroscopies, and crystallography. 4-Methylpyridine-2-thiol interacts with chloride ions in acetonitrile to form a salt called methylpyridinium chloride.</p>Formula:C6H7NSPurity:Min. 95%Molecular weight:125.19 g/mol3-(3,4-Difluorophenyl)-3-methylpyrrolidine
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H13F2NPurity:Min. 95%Molecular weight:197.22 g/mol1-(4-Methylphenyl)-3-(prop-2-yn-1-yl)urea
CAS:<p>1-(4-Methylphenyl)-3-(prop-2-yn-1-yl)urea is a fluorescent derivative that can be detected with certain techniques. It has been used to detect phosphatases in cervical cancer cells and tumor cells. This compound is a ligand for the surface antigen of placental alkaline phosphatase (PLAP). It can also bind to other organic ligands, such as recombinant human erythropoietin (EPO), which may be useful for redirecting the action of this protein. 1-(4-Methylphenyl)-3-(prop-2-yn-1-yl)urea is an organic bispecific molecule that binds to two receptors, one on tumor cells and one on normal cells. This binding leads to cell death by apoptosis through the release of cytochrome c from mitochondria.</p>Formula:C11H12N2OPurity:Min. 95%Molecular weight:188.23 g/mol(2S,5S)-1-{[(9H-Fluoren-9-yl)methoxy]carbonyl}-5-phenylpyrrolidine-2-carboxylic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C26H23NO4Purity:Min. 95%Molecular weight:413.5 g/molRef: 3D-UYB95360
Discontinued product1-({2-Methyl-5H,6H,7H,8H-imidazo[1,2-a]pyridin-3-yl}methyl)piperazine
CAS:<p>Versatile small molecule scaffold</p>Formula:C13H22N4Purity:Min. 95%Molecular weight:234.34 g/molRef: 3D-CHC38025
Discontinued productrac-Methyl (1R,2R)-1-amino-2,3-dihydro-1H-indene-2-carboxylate hydrochloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H14ClNO2Purity:Min. 95%Molecular weight:227.7 g/molRef: 3D-FCA27000
Discontinued productPB-22 3-carboxyindole metabolite solution
CAS:Controlled Product<p>PB-22 is a synthetic cannabinoid, which can be classified as a CB1 receptor agonist. It is one of the many cannabinoids that have been created in an attempt to circumvent drug laws by creating compounds that are similar to those found in cannabis but have different chemical structures. PB-22 has shown to increase locomotor activity and stimulate the cb1 receptor in mice. Magnetic resonance spectroscopy (MRS) and assays were used to determine the binding affinity of PB-22 for the CB1 receptor. The MRS data showed that PB-22 bound with high affinity to the CB1 receptor and had a lower affinity for CB2 receptors. This suggests that PB-22 may be more potent than other synthetic cannabinoids, such as JWH-018 and CP 55,940, which bind better with CB2 receptors than CB1 receptors.<br>PB-22 is an analog of JWH-073 and has been shown to have a stronger effect on locomotor activity than JWH</p>Formula:C14H17NO2Purity:Min. 95%Molecular weight:231.29 g/mol3,8-Dioxa-11-azaspiro[5.6]dodecane
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H17NO2Purity:Min. 95%Molecular weight:171.24 g/molRef: 3D-WQC17744
Discontinued product2-Bromo-3,3,3-trifluoro-1-propene
CAS:Controlled Product<p>2-Bromo-3,3,3-trifluoro-1-propene is a chemical compound that has been synthesized in an asymmetric reaction. The reactant is bromopropane and the product is 2,2,2-trifluoropropene. The methylene group on the propene molecule is activated by the nucleophilic attack of a fluoride ion from hydrogen fluoride to form a cavity with a highly strained bond. The kinetic study of this reaction revealed that the activation energy for the reaction is 42 kJ/mol. Palladium-catalyzed coupling reactions are catalyzed by palladium and require nonpolar solvents such as toluene or dichloromethane. This type of reaction has been shown to be exothermic with an isolated yield of 1%.</p>Formula:C3H2BrF3Purity:Min. 95%Color and Shape:Colorless PowderMolecular weight:174.95 g/mol3-Boc-3-azabicyclo[3.2.1]octan-8-amine
CAS:<p>Versatile small molecule scaffold</p>Formula:C12H22N2O2Purity:Min. 95%Molecular weight:226.32 g/mol
