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-Amino-2-(4-chlorophenyl)propanoic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H10ClNO2Purity:Min. 95%Molecular weight:199.63 g/mol1-Hydroxy-3-(4-hydroxy-3-methoxyphenyl)propan-2-one
CAS:<p>1-Hydroxy-3-(4-hydroxy-3-methoxyphenyl)propan-2-one is a chemical compound that belongs to the group of phenols. It is an intermediate in the production of lignin, which is used in the manufacture of paper and other products. The chemical structure of 1-hydroxy-3-(4-hydroxy-3 methoxyphenyl)propan-2-one can be found in coniferous plants such as pine trees, where it is generated by oxidative coupling of 4 hydroxycinnamaldehyde and 3 hydroxybenzaldehyde.</p>Formula:C10H12O4Purity:Min. 95%Molecular weight:196.2 g/mol1-Methoxy-4-nitronaphthalene
CAS:<p>1-Methoxy-4-nitronaphthalene is a yellow crystalline solid that belongs to the group of naphthalenes. It reacts with deionized water to give nitronaphthalene, which can be detected by ultrafast spectroscopy at constant temperature or by second-order rate constants. The nitro group can be reduced to an amine on treatment with phosphite or diphosphorylated. Nitro groups are also susceptible to nucleophilic attack by acetonitrile and ammonium nitrate, and can be photoreduced to the corresponding amino compound.</p>Formula:CH3OC10H6NO2Purity:Min. 95%Molecular weight:203.19 g/mol4-Oxo-1,4-dihydro-1,6-naphthyridine-3-carboxylic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H6N2O3Purity:Min. 95%Molecular weight:190.16 g/molrac-(1R,2R)-2-(Pyridin-4-yl)cyclopropane-1-carboxylic acid hydrochloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H10ClNO2Purity:Min. 95%Molecular weight:199.6 g/molrac-(1R,2S)-2-(Pyridin-4-yl)cyclopropane-1-carboxylic acid hydrochloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H10ClNO2Purity:Min. 95%Molecular weight:199.6 g/molα-Acetyltetrahydro-3-thiopheneacetic acid ethyl ester 1,1-dioxide
CAS:Versatile small molecule scaffoldFormula:C10H16O5SPurity:Min. 95%Molecular weight:248.3 g/molN,N,3,5-Tetramethylaniline
CAS:<p>N,N,3,5-Tetramethylaniline is a colorless liquid that is soluble in water. It has an aromatic odor and is used as a solvent. N,N,3,5-Tetramethylaniline has been shown to react with 4-dimethylaminobenzoic acid to form a thioxanthone by an irreversible oxidation process. This reaction requires activation energies of 34.2 kcal/mol for the initiation step and 17.1 kcal/mol for termination. The reaction mechanism can be described as:</p>Formula:C10H15NPurity:Min. 95%Molecular weight:149.24 g/mol2-Benzyl-1H-imidazol-4(5H)-one
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H10N2OPurity:Min. 95%Molecular weight:174.2 g/mol1-(4-Methoxyphenyl)-1H-1,2,3-triazole-4-carboxylic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H11N3O3Purity:Min. 95%Molecular weight:233.22 g/mol3-Hydroxy-2,2,4,4-tetramethylcyclobutan-1-one
CAS:<p>3-Hydroxy-2,2,4,4-tetramethylcyclobutan-1-one is a monomer that is soluble in organic solvents. It can be isolated by centrifugation of the reaction mixture and purified by filtration or recrystallization. 3-Hydroxy-2,2,4,4-tetramethylcyclobutan-1-one has been used as a catalyst for the polymerization of ethylene oxide to polyethers. 3-Hydroxy-2,2,4,4-tetramethylcyclobutan-1-one is also an excellent solvent for ruthenium metal and can be used as a reaction solvent for reactions involving this metal.</p>Formula:C8H14O2Purity:Min. 95%Molecular weight:142.2 g/mol2-(3-Methylcyclohexyl)ethan-1-ol
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H18OPurity:Min. 95%Molecular weight:142.24 g/mol2-(4-Methylcyclohexyl)ethan-1-ol
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H18OPurity:Min. 95%Color and Shape:Clear LiquidMolecular weight:142.24 g/mol2-(Cyclopropylamino)-1-phenylethan-1-ol hydrochloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H16ClNOPurity:Min. 95%Molecular weight:213.7 g/molDimenhydrinate Related Compound E
CAS:Controlled Product<p>Dimenhydrinate Related Compound E is a test compound that has shown potentiation of the inhibitory properties of hydrochloric acid against a variety of enzymes. This compound inhibits the enzyme activity of cyclooxygenase-1 (COX-1) and COX-2, which are important in the production of prostaglandins. Dimenhydrinate Related Compound E also has anticancer activity, which may be due to its ability to cause DNA damage by inhibiting the synthesis of proteins needed for cell replication. The use of this compound may have genotoxic effects and chronic exposure should be avoided.</p>Formula:C8H9ClN4O2Purity:Min. 95%Molecular weight:228.64 g/mol3,7-Dimethyl-2,6-dioxo-2,3,6,7-tetrahydro-1H-purine-8-carbaldehyde
CAS:Versatile small molecule scaffoldFormula:C8H10N4O3Purity:Min. 95%Molecular weight:210.19 g/mol8-Chloro-3,7-dimethyl-2,3,6,7-tetrahydro-1H-purine-2,6-dione
CAS:Controlled Product<p>Versatile small molecule scaffold</p>Formula:C7H7ClN4O2Purity:Min. 95%Molecular weight:214.61 g/mol4-(4H-1,2,4-Triazol-3-yl)aniline
CAS:<p>Versatile small molecule scaffold</p>Formula:C8H8N4Purity:Min. 95%Molecular weight:160.18 g/mol5-(Thiophen-2-yl)-4H-1,2,4-triazol-3-amine
CAS:<p>Versatile small molecule scaffold</p>Formula:C6H6N4SPurity:Min. 95%Molecular weight:166.21 g/mol2-Chloro-3-nitroimidazo[1,2-a]pyridine
CAS:<p>2-Chloro-3-nitroimidazo[1,2-a]pyridine is a chlorinated derivative of imidazo[1,2-a]pyridine. The nitro group gives the molecule two sites for functionalization and enables it to undergo Suzuki coupling reactions with anilines. The chloro substituent provides the molecule with a high degree of chemical diversity. This compound can be used in cross-coupling reactions with anilines and other heterocycles, such as thiophenes and furans. In addition, this compound has been shown to react with nucleophiles in a nucleophilic substitution reaction to form 2-chloro-5-(substituted)imidazo[1,2-a]pyridinium ions.</p>Formula:C7H4ClN3O2Purity:Min. 95%Molecular weight:197.58 g/mol
