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(5,780 products)
- Chiral Building Blocks(1,241 products)
- Hydrocarbon Building Blocks(6,100 products)
- Organic Building Blocks(61,029 products)
Found 205306 products of "Building Blocks"
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3-Cyclohexylaniline
CAS:Versatile small molecule scaffold
Formula:C12H17NPurity:Min. 95%Molecular weight:175.27 g/molEthyl 3,3-dimethyloxirane-2-carboxylate
CAS:Versatile small molecule scaffold
Formula:C7H12O3Purity:Min. 95%Molecular weight:144.17 g/mol(2Z)-(2,4-Dioxo-1,3-thiazolidin-5-ylidene)acetic acid
CAS:Versatile small molecule scaffoldFormula:C5H3NO4SPurity:Min. 95%Molecular weight:173.15 g/mol1-Benzyloxy-3-iodopropane
CAS:1-Benzyloxy-3-iodopropane is an enantiopure prenyl alcohol, which can be used in the alkylation of unsaturated fatty acids. It has been used to synthesize pseudoephedrine with yields of up to 97% and chirality that is stereospecific and enantiopure. In addition, it can be used as a reagent for biomolecular studies.Formula:C10H13IOPurity:Min. 95%Molecular weight:276.11 g/mol4-(1,3,4-Oxadiazol-2-yl)phenol
CAS:4-(1,3,4-Oxadiazol-2-yl)phenol (ODOP) is a potent and selective apoptosis inducer that causes the death of cancer cells by generating reactive oxygen species. ODOP activates polyphosphoric acid in the mitochondria to form reactive oxygen species. The cytotoxicity of ODOP is dose-dependent and can be reconfirmed by nucleophilic attack on DNA. ODOP has been shown to have pharmacokinetic properties that are similar to those of other drugs in the same class, such as acylhydrazides. These drugs are rapidly metabolized by esterases or glucuronidases in vivo and are excreted mainly through urine.Formula:C8H6N2O2Purity:Min. 95%Molecular weight:162.15 g/mol2-(3-Chlorophenyl)-1,3,4-oxadiazole
CAS:Versatile small molecule scaffoldFormula:C8H5ClN2OPurity:Min. 95%Molecular weight:180.59 g/mol2,3-Dihydro-1-benzofuran-3-ol
CAS:Versatile small molecule scaffoldFormula:C8H8O2Purity:Min. 95%Molecular weight:136.15 g/mol3-(Hydroxymethyl)benzo[b]thiophene
CAS:3-(Hydroxymethyl)benzo[b]thiophene is a potential anticancer agent that inhibits the PI3K/Akt pathway. It has been shown to have cytotoxic effects on colorectal adenocarcinoma cells, as well as other cancer cells. 3-(Hydroxymethyl)benzo[b]thiophene also binds to DNA and alters the structure of the double helix, leading to inhibition of DNA synthesis, which may lead to cell death. The compound has been tested in vitro and found to be effective against leukemia and colon cancer cells. It has also shown anticancer activity in vivo in mice, with no observable side effects or toxicity.Formula:C9H8OSPurity:Min. 95%Molecular weight:164.22 g/mol2,2-Bis(chloromethyl)butan-1-ol
CAS:Versatile small molecule scaffold
Formula:C6H12Cl2OPurity:Min. 95%Molecular weight:171.06 g/mol1,3-Diphenylpropan-2-ol
CAS:1,3-Diphenylpropan-2-ol is an organic molecule that can be used in analytical toxicology. It has been shown to have a nonequivalence of 1,3-diphenylpropane and 2-hydroxypentane. The functional groups present on this molecule are the silicon atom and the organic acids. This molecule is metastable due to its radical coupling. 1,3-Diphenylpropan-2-ol is found in a number of chemical reactions including bond cleavage, aldehyde formation, alkene formation, and asymmetric synthesis. Cleavage products include 3-phenylpropanoic acid, phenylacetic acid, and phenylglycolic acid.
Formula:C15H16OPurity:Min. 95%Molecular weight:212.29 g/mol2-Cyano-N-(4-methoxyphenyl)acetamide
CAS:2-Cyano-N-(4-methoxyphenyl)acetamide is a synthetic compound with inhibitory effects on the enzyme dipeptidyl peptidase IV (DPP-IV). This enzyme is involved in the degradation of incretins, such as glucagon-like peptide 1 (GLP-1), and has been implicated in the development of type 2 diabetes mellitus. The synthesis and characterization of this compound was reported in a paper published in 2000. It has been shown to be a potent inhibitor of DPP-IV, with IC50 values of 0.10 μM for rat pancreatic DPP-IV and 0.06 μM for human recombinant enzyme. The effects of this compound on GLP-1 levels were also studied, showing that it had no effect on basal levels but significantly increased postprandial GLP-1 secretion.Formula:C10H10N2O2Purity:Min. 95%Molecular weight:190.2 g/molN-(4-Carboxyphenyl)phthalimide
CAS:N-(4-Carboxyphenyl)phthalimide is a ligand that interacts with metal ions. It has been shown to bind to benzocaine and dihedral angles in polyvinyl chloride, lysine, and hydrogen bonds in hydrogen-bonded complexes. N-(4-Carboxyphenyl)phthalimide has been used as a bifunctional agent for the polymerization of vinyl chloride.Formula:C15H9NO4Purity:Min. 95%Molecular weight:267.24 g/mol1-(2-Hydroxy-3,4-dimethylphenyl)ethan-1-one
CAS:Versatile small molecule scaffoldFormula:C10H12O2Purity:Min. 95%Molecular weight:164.2 g/molTricyclo[7.2.1.0,2,7]dodeca-2,4,6-trien-8-one
CAS:Versatile small molecule scaffoldFormula:C12H12OPurity:Min. 95%Molecular weight:172.2 g/molTizanidine Related Compound C
CAS:Versatile small molecule scaffoldFormula:C5H8N2OSPurity:Min. 95%Molecular weight:144.19 g/mol1-Phenylhexan-3-amine
CAS:Versatile small molecule scaffoldFormula:C12H19NPurity:Min. 95%Molecular weight:177.29 g/mol2-Bromobenzothiophene
CAS:2-Bromobenzothiophene (BBT) is a synthetic molecule that has potent inhibitory activity against several biological targets, including hydroxy group, enantiomer and enhancement. BBT has been shown to have anticancer properties in vitro and in vivo. This compound also exhibits anti-inflammatory activities, which may be mediated by the inhibition of inflammatory cytokines such as IL-6, IL-8 and TNF-α. This heterocycle inhibits estradiol binding to estrogen receptors by competitive inhibition. The hydroxyl group on 2-bromobenzothiophene can form a covalent bond with thiols, which are abundant in proteins involved in inflammation. It also reacts with other reactive functional groups such as carbonyl groups or aromatic hydrocarbons.
Formula:C8H5BrSPurity:Min. 95%Molecular weight:213.09 g/mol4,7-Dichloro-1,10-phenanthroline
CAS:4,7-Dichloro-1,10-phenanthroline is a bidentate ligand that binds to the chloride anion and has been shown to have anticancer activity against leukemia cells. This compound has also been shown to inhibit the proliferation of cervical cancer cells and chronic myeloid leukemia cells. 4,7-Dichloro-1,10-phenanthroline enhances the fluorescence of human chronic myeloid leukemia cells in a cytometry assay by increasing hydrogen bonding between the cell membrane and fluorophore. This enhancement effect was seen at concentrations of 0.01 μM and higher. 4,7-Dichloro-1,10-phenanthroline also binds to DNA and has been shown to be effective against cancer cells in a luminescent human chronic myeloid leukemia (MRC5) assay.
Formula:C12H6Cl2N2Purity:Min. 95%Molecular weight:249.09 g/mol4-(2,5-Dimethylphenyl)-4-oxobutanoic acid
CAS:Versatile small molecule scaffoldFormula:C12H14O3Purity:Min. 95%Molecular weight:206.24 g/mol2-Phenyl-2-(propan-2-yloxy)acetic acid
CAS:2-Phenyl-2-(propan-2-yloxy)acetic acid (PPAA) is a serotonin antagonist that inhibits the binding of serotonin to its receptor. PPAA has been shown to have anti-cancer and anti-inflammatory properties. It also has antagonistic properties against azabicyclic compounds, organic acids, and tachykinin peptides. PPAA has also been found to be a prodrug for the treatment of Parkinson's disease, with the active form being 2-(benzyloxy)-2-phenylethanoic acid. The molecular weight of PPAA is 220.21 g/mol and it is soluble in water. PPAA can be synthesized from piperidine and benzyl group with amide as a byproduct. The oxygen atoms in PPAA are c1-c6 alkoxy which are esterified by propan-2-ol.Formula:C11H14O3Purity:Min. 95%Molecular weight:194.23 g/mol2-Bromo-N-propylacetamide
CAS:2-Bromo-N-propylacetamide is a protein target that has been shown to regulate the activity of amines. It has affinity for both anionic and cationic amines. 2-Bromo-N-propylacetamide is used in optimization studies to identify the fluorescent groups that can be used as labels on proteins. This drug also interacts with family members, such as elution and immobilization.Formula:C5H10BrNOPurity:Min. 95%Molecular weight:180.04 g/mol(4-Chlorophenyl)(4-methylphenyl)methanone
CAS:Versatile small molecule scaffoldFormula:C14H11ClOPurity:Min. 95%Color and Shape:PowderMolecular weight:230.69 g/molEthyl oxo(2-oxocyclohexyl)acetate
CAS:Ethyl oxo(2-oxocyclohexyl)acetate is a condensation product of glycine and anhydride, which is obtained by heating the two components in the presence of acid. The reaction yields an isomeric mixture of ethyl oxo(2-oxocyclohexyl)acetate and ethyl oxo(3-oxocyclohexyl)acetate. The condensation products are hydrolyzed to their respective amino acids with ammonia or sodium hydroxide. Ethyl oxo(2-oxocyclohexyl)acetate can also be synthesized from glycine ethyl ester and aminomalonic acid in the presence of enamine.Formula:C10H14O4Purity:Min. 95%Molecular weight:198.22 g/mol6,9-Dichloro-1,2,3,4-tetrahydroacridine
CAS:Versatile small molecule scaffoldFormula:C13H11Cl2NPurity:Min. 95%Molecular weight:252.14 g/mol2-(tert-Butylsulfanyl)ethan-1-ol
CAS:Versatile small molecule scaffold
Formula:C6H14OSPurity:Min. 95%Molecular weight:134.24 g/mol1-Chloro-3-phenylpropan-2-ol
CAS:1-Chloro-3-phenylpropan-2-ol is an alcohol that is detectable and has been shown to have a stereoselective dehydrogenase activity. The kinetic parameters of this enzyme are optimal for the detection of 1-chloro-3-phenylpropan-2-ol in complex mixtures. It has been used in pharmaceuticals as a chiral building block, where it forms a ternary complex with a chiral metal ion and an amino acid. This enzyme is also able to catalyze the conversion of phenylacetone into amphetamine.
Formula:C9H11ClOPurity:Min. 95%Molecular weight:170.63 g/mol1,5-Diphenylpentan-3-one
CAS:1,5-Diphenylpentan-3-one is a hydroxylated analog of the anti-inflammatory compound 1,5-diphenylpentan-2-one. It can be used as a reactive intermediate in the synthesis of ester compounds, hydrogen bond inhibitors, and insulin resistance inhibitors. This compound also has the ability to inhibit HDAC activity and radiation.Formula:C17H18OPurity:Min. 95%Molecular weight:238.32 g/mol5-(4-Chlorophenyl)-5-methylimidazolidine-2,4-dione
CAS:Versatile small molecule scaffoldFormula:C10H9ClN2O2Purity:Min. 95%Molecular weight:224.64 g/mol6-Methyl-3,4-dihydro-2H-pyran-5-carboxylic acid
CAS:6-Methyl-3,4-dihydro-2H-pyran-5-carboxylic acid is an organic compound that is used as a solvent. It is preferentially soluble in solvents with low boiling points and high dielectric constants. The solvation of 6-methylpyran-5-carboxylic acid can be accomplished by photooxygenation or hydroperoxide formation.Formula:C7H10O3Purity:Min. 95%Molecular weight:142.15 g/mol4-Sulfobenzoic acid potassium
CAS:4-Sulfobenzoic acid potassium salt is a quasicrystalline compound with a flow rate of 0.1 cm/s. It is a molecule with an approximate diameter of 2 nm and functional groups that include sulfonic acid, carboxylic acid, hydroxyl, and OH. 4-Sulfobenzoic acid potassium salt has a high solubility in water and can be found in the form of potassium ions or as a covalent bond to other molecules. The analytical methods for this compound include IR (infrared) spectroscopy, Raman spectroscopy, X-ray diffraction analysis, and electron microscopy. A synthetic method for 4-sulfobenzoic acid potassium salt is via reaction of benzoic acid with potassium hydroxide followed by recrystallization from ethanol. This compound can be found in the form of nanosheets or polymerized into polybenzoxazole filmsFormula:C7H6O5S•KPurity:Min. 95%Molecular weight:241.28 g/mol7-Chloro-3-methyl-1H-pyrazolo[4,3-d]pyrimidine
CAS:Formycin is a form of potassium glycolate (KG), which belongs to the class of chlorinated alkyl ethers. Formycin has been used as an antiseptic, but is no longer in use due to its toxicity. It is also a potent inhibitor of bacterial growth and was used in the past for treating tuberculosis. The methylation of KG produces formaldehyde, which can react with ethylene glycol to produce ethylene glycol monomethyl ether (EGME). EGME is highly toxic and can cause lung damage.Formula:C6H5ClN4Purity:Min. 95%Molecular weight:168.58 g/mol3-(4-Methylphenyl)propan-1-ol
CAS:3-(4-Methylphenyl)propan-1-ol is a compound that is used as an intermediate in organic synthesis. It has been shown to undergo regioselective radical cyclization reactions with cations and radical cations, yielding the corresponding methylenecyclopropane derivatives. 3-(4-Methylphenyl)propan-1-ol can be used as a precursor for various other compounds, such as ethyl (2E)-3-[4-(methylphenyl)buta-1,3-diene]propanoate.Formula:C10H14OPurity:Min. 95%Molecular weight:150.22 g/mol7-Methyloctan-3-one
CAS:7-Methyloctan-3-one is a natural product that belongs to the family of cyclic terpenes. It has been identified in the fur of the arctic fox and has been shown to be a pheromone in some species of formicidae (ants). The compound is also found in tarandus (reindeer) and formicidae species. 7-Methyloctan-3-one exhibits an endoparasitic effect on insects, including those that are pests for humans such as the Colorado potato beetle, and can be used as an insecticide. The compound is hypothesized to have a similar effect on other types of pests, including mites and ticks. 7-Methyloctan-3-one is extracted by distillation from animal fat or vegetable oils with high boiling points. Chromatographic analysis reveals its presence at Rf 0.4 on TLC plates with a solvent system of hexane/diethyl ether/Formula:C9H18OPurity:Min. 95%Molecular weight:142.24 g/mol1-(2-chlorophenyl)-2-methylpropan-1-one
CAS:Versatile small molecule scaffoldFormula:C10H11OClPurity:Min. 95%Molecular weight:182.64 g/mol2,3-Dibromobutane
CAS:2,3-Dibromobutane is a molecule that is used as a polarizer in liquid crystal composition. It is an elimination reaction product of bromine and ethylene, which also has the ability to inhibit hyperproliferative diseases. 2,3-Dibromobutane has been shown to have cancer-preventing properties by inhibiting the growth of tumor cells. The mechanism of this inhibition is not yet clear and may be due to its ability to react with reactive oxygen species or other intermediates involved in carcinogenesis. 2,3-Dibromobutane has been shown to form adducts with protonated molecules such as phenol or cresol, which are found in coal tar and cigarette smoke. These adducts have been shown to cause mutations and increase the risk for cancer.Formula:C4H8Br2Purity:Min. 95%Molecular weight:215.92 g/molBis[(pinacolato)boryl]methane
CAS:Bis[(pinacolato)boryl]methane is a bifunctional organoboron reagent with an allyl group on one end and a cyclopropane on the other end. It is useful in organic synthesis as a nucleophile for allylation, as well as for the synthesis of unsymmetrical cyclopropanes. This compound can be used to catalyze asymmetric methods, such as the synthesis of alicyclic compounds. Bis[(pinacolato)boryl]methane can also be used to synthesize biomolecules.Formula:C13H26B2O4Purity:Min. 95%Color and Shape:White To Off-White SolidMolecular weight:267.97 g/molBis[2-(perfluorooctyl)ethyl] phosphate
CAS:Controlled ProductBis[2-(perfluorooctyl)ethyl] phosphate is a perfluorinated compound that can be used as an alternative to polyvinyl chloride in the manufacture of children's toys and other consumer products. It has been shown to have no health effects on humans, unlike other perfluorinated compounds, in a study where human serum was analyzed. Bis[2-(perfluorooctyl)ethyl] phosphate also has a high affinity for polyfluoroalkyl substances (PFASs) and can be used in analytical methods for their detection. The optimised extraction procedure is simple and rapid, using ultrasonic extraction with no need for any organic solvents. Recoveries are high (>99%) and the method does not require any volatile solvents.Formula:C20H9F34O4PPurity:Min. 95%Molecular weight:990.2 g/molBenzenesulfonyl chloride
CAS:Benzenesulfonyl chloride is an antimicrobial agent that inhibits the enzyme Cox-2. It has been shown to be a potent anti-cancer compound in laboratory studies and has been found to have anti-inflammatory properties. Benzenesulfonyl chloride may also be effective against metabolic disorders such as obesity, diabetes, and cancer. The mechanism of action is currently unclear, but it has been shown to inhibit the activity of human serum xanthine oxidase, which is involved in oxidation reactions. This inhibition may lead to a decrease in the production of reactive oxygen species (ROS) that are toxic to cells. The reaction between benzenesulfonyl chloride and sulfonyl chloride is as follows: Benzenesulfonyl chloride + Sulfonyl chloride → Benzenesulfonic acid + Chlorosulfonic acidFormula:C6H5ClO2SPurity:Min. 95%Color and Shape:Clear LiquidMolecular weight:176.62 g/mol2-(Bromomethyl)-5-nitrofuran
CAS:2-(Bromomethyl)-5-nitrofuran is a hydroxyl-containing molecule that is able to target hypoxic tumor sites. It has been shown to be effective against ges-1 cells, which are the most common cell type in the bone marrow and are resistant to chemotherapy. 2-(Bromomethyl)-5-nitrofuran causes DNA damage by reacting with amines, such as methylamine, and nucleophilic groups, such as thiols. This molecule also has antibacterial properties, which may be due to its ability to react with bacterial cytochrome P450 enzymes. 2-(Bromomethyl)-5-nitrofuran can be synthesized from commercially available starting materials in an economically feasible manner.Formula:C5H4BrNO3Purity:Min. 97 Area-%Color and Shape:White PowderMolecular weight:205.99 g/mol1-Bromo-3-chloropropane
CAS:1-Bromo-3-chloropropane is a chemical that has been used in the synthesis of various organic compounds. It has been shown to exhibit neurotoxicity, as well as to be carcinogenic and mutagenic. The compound can also affect the central nervous system by decreasing locomotor activity. It has also been shown to cause respiratory problems in rats, and may be toxic if inhaled or ingested. 1-Bromo-3-chloropropane exhibits cytotoxic effects on human cells grown in vitro, which may be due to its ability to bind nucleophilic groups on proteins. This reaction is thought to yield an acylated product with a chloride ion at one terminus and a methyl anthranilate at the other terminus.Formula:C3H6BrClPurity:Min. 98 Area-%Color and Shape:Colorless Clear LiquidMolecular weight:157.44 g/mol4-Bromo-3,5-dimethylbenzoic acid methyl ester
CAS:4-Bromo-3,5-dimethylbenzoic acid methyl ester is a versatile building block that is used in the synthesis of complex compounds. 4-Bromo-3,5-dimethylbenzoic acid methyl ester is an intermediate in the synthesis of speciality chemicals and research chemicals. It is also a useful scaffold for the synthesis of high quality and useful reagents as well as reaction components.Formula:C10H11BrO2Purity:Min. 95%Color and Shape:White PowderMolecular weight:243.1 g/mol3-Phenyl-2-propyn-1-amine hydrochloride
CAS:3-Phenyl-2-propyn-1-amine hydrochloride is a dopamine β-hydroxylase inhibitor that can be detected in urine. It is used to study the effects of various drugs and chemicals on the metabolism of dopamine, noradrenaline, and other catecholamines. 3PPPA has been shown to inhibit the activity of cytochrome P450 enzymes and blocks adrenergic receptors. This drug also inhibits the synthesis of epinephrine from norepinephrine by blocking its conversion to epinephrine. 3PPPA may also be used as a receptor blocker for diagnosis or treatment of asthma or allergic reactions by preventing the release of histamine, which is released from mast cells in response to an allergen, causing inflammation.Formula:C9H10ClNPurity:Min. 95%Molecular weight:167.64 g/mol2-(2-Methylthiophen-3-yl)acetic acid
CAS:Versatile small molecule scaffoldFormula:C7H8O2SPurity:Min. 95%Molecular weight:156.2 g/mol7-Methoxy-4-phenyl-1,2-dihydroquinolin-2-one
CAS:Versatile small molecule scaffoldFormula:C16H13NO2Purity:Min. 95%Molecular weight:251.28 g/mol2-(4-Ethoxy-1H-indol-3-yl)acetonitrile
CAS:Versatile small molecule scaffold
Formula:C12H12N2OPurity:Min. 95%Molecular weight:200.24 g/mol2-Methylpropyl 4-oxopiperidine-1-carboxylate
CAS:Controlled ProductVersatile small molecule scaffoldFormula:C10H17NO3Purity:Min. 95%Molecular weight:199.25 g/mol4-(4-Chlorobenzenesulfonyl)-1H-pyrazol-5-amine
CAS:Versatile small molecule scaffoldFormula:C9H8ClN3O2SPurity:Min. 95%Molecular weight:257.7 g/molEthyl 1-bromocyclopentane-1-carboxylate
CAS:Versatile small molecule scaffoldFormula:C8H13BrO2Purity:Min. 95%Molecular weight:221.09 g/molEthyl 2-(4-cyanophenoxy)acetate
CAS:Versatile small molecule scaffold
Formula:C11H11NO3Purity:Min. 95%Molecular weight:205.21 g/mol4-(4-Chlorophenyl)morpholine-2,6-dione
CAS:Versatile small molecule scaffold
Formula:C10H8ClNO3Purity:Min. 95%Molecular weight:225.63 g/mol
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