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(5,778 products)
- Chiral Building Blocks(1,242 products)
- Hydrocarbon Building Blocks(6,098 products)
- Organic Building Blocks(61,084 products)
Found 198714 products of "Building Blocks"
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Methyl 1-methyl-1H-pyrazole-3-carboxylate
CAS:Versatile small molecule scaffoldFormula:C6H8N2O2Purity:Min. 95%Molecular weight:140.14 g/mol4-(4-Aminophenyl)benzene-1,2-diamine
CAS:<p>4-(4-Aminophenyl)benzene-1,2-diamine (4-APB) is a neuroprotective agent that has been shown to protect neurons in vitro against oxidative stress and glutamate toxicity. 4-APB also inhibits the uptake of 4-(4-aminophenyl)benzene-1,2-diamine into cells by inhibiting the enzyme responsible for its synthesis. This inhibition leads to a decrease in cellular levels of 4-(4-aminophenyl)benzene-1,2-diamine and an increase in its concentration outside the cell. It has been shown to be effective against human ovarian carcinoma cells and ascitic cancer cells, but not against cisplatin resistant cancer cells. The mechanism of action of this drug is still unknown.</p>Formula:C12H13N3Purity:Min. 95%Molecular weight:199.25 g/mol4-Chloro-2H-chromen-2-one
CAS:<p>4-Chloro-2H-chromen-2-one is an organic compound that is used as a building block in the synthesis of coumarin derivatives. It undergoes nucleophilic substitution reactions with amines, forming 4-hydroxycoumarin. This reaction is catalyzed by organometallic compounds such as PdCl2 and Cu(OAc)2. Cross-coupling reactions have been shown to be effective for the synthesis of coumarin derivatives. The mechanism of this reaction involves oxidative addition of an organometallic reagent to the carbon atom, followed by elimination of water to form an intermediate epoxide. Deuteration is required for this reaction because hydrogen reacts too rapidly with the organometallic reagents to be useful in the coupling process. 4-Chloro-2H-chromen-2-one has been shown to react with other nucleophiles such as thiols, phenols, and alcohols at</p>Formula:C9H5ClO2Purity:Min. 95%Molecular weight:180.59 g/molN-Ethyl-2,2-dimethyl-1-propanamine hydrochloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H18ClNPurity:Min. 95%Molecular weight:151.68 g/mol2-(Prop-2-en-1-ylsulfanyl)benzoic acid
CAS:<p>2-(Prop-2-en-1-ylsulfanyl)benzoic acid is a phenyl group that has the ability to form a desorption molecule. It is light resistant and photopolymerizable, which means it can be used in the production of polymers. The alkylthio group on this molecule allows for transfer and gel permeation chromatography. 2-(Prop-2-en-1-ylsulfanyl)benzoic acid also has a vinylic group, which makes it hydrosilylation crosslinkable. This makes it an excellent candidate for copolymerization and hydrosilylation.</p>Formula:C10H10O2SPurity:Min. 95%Molecular weight:194.25 g/mol2-(Isobutyrylamino)benzoic acid
CAS:Versatile small molecule scaffoldFormula:C11H13NO3Purity:Min. 95%Molecular weight:207.23 g/mol4-(Aminomethyl)benzohydrazide hydrochloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C8H12ClN3OPurity:Min. 95%Molecular weight:201.65 g/molEthyl 4-(aminomethyl)phenylacetate hydrochloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H16ClNO2Purity:Min. 95%Molecular weight:229.7 g/mol4-Dimethylaminomethyl-benzoic acid hydrochloride
CAS:<p>4-Dimethylaminomethyl-benzoic acid hydrochloride (4DMABAH) is an antiviral agent that inhibits the replication of human immunodeficiency virus type 1 (HIV-1) by blocking the synthesis of viral DNA. 4DMABAH is a prodrug, which is metabolized to its active form, lamivudine, by esterases in the liver and other tissues. 4DMABAH has been shown to be effective against hepatitis B and C viruses in cell culture studies.</p>Formula:C10H14ClNO2Purity:Min. 95%Molecular weight:215.68 g/mol3,4-Dichloro-N-propylbenzene-1-sulfonamide
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H11Cl2NO2SPurity:Min. 95%Molecular weight:268.16 g/mol2-Chloro-3-phenylpropanenitrile
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H8ClNPurity:Min. 95%Molecular weight:165.62 g/mol1,2-Dibromo-3-methylbut-2-ene
CAS:<p>Versatile small molecule scaffold</p>Formula:C5H8Br2Purity:Min. 95%Molecular weight:227.92 g/molPentane-2-sulfonamide
CAS:<p>Versatile small molecule scaffold</p>Formula:C5H13NO2SPurity:Min. 95%Molecular weight:151.23 g/molButane-2-sulfonamide
CAS:<p>Versatile small molecule scaffold</p>Formula:C4H11NO2SPurity:Min. 95%Molecular weight:137.2 g/mol4-(Methylsulfanyl)benzene-1,2-diamine
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H10N2SPurity:Min. 95%Molecular weight:154.24 g/mol1,4-Benzodioxine-2-carboxylic acid
CAS:<p>1,4-Benzodioxine-2-carboxylic acid is a synthetic compound that is a member of the c1-6 alkyl group. It has been synthesized in four different stereoisomers, including cis and trans isomers. 1,4-Benzodioxine-2-carboxylic acid has potent inhibitory effects on protein synthesis in cell preparations at multigram concentrations. It also inhibits the activity of translation or replication of DNA or RNA by binding to the active site of the enzyme ribonuclease H and inhibiting its cleavage at the 3'-terminal nucleotide bonds. The trifluoromethyl group on 1,4-benzodioxine-2-carboxylic acid may be responsible for some of its biological properties. Molecular modeling studies have shown that 1,4 benzodioxine carboxylic acid binds to DNA through hydrogen bonding with one water molecule and two guanidine</p>Formula:C9H6O4Purity:Min. 95%Molecular weight:178.14 g/mol5-Ethoxy-1,2,4-thiadiazole-3-carboxylic acid
CAS:<p>5-Ethoxy-1,2,4-thiadiazole-3-carboxylic acid (ETT) is a metabolite of etridiazole. Etridiazole is an antihelminthic drug that is used in the treatment of intestinal roundworm infections. ETT has been shown to be excreted in urine and can be used as an analytical marker for monitoring etridazole use.</p>Formula:C5H6N2O3SPurity:Min. 95%Molecular weight:174.18 g/mol4-Hydroxymethylbenzenesulfonamide
CAS:<p>4-Hydroxymethylbenzenesulfonamide is a potent carbonic anhydrase inhibitor that has been shown to be effective against a number of different microorganisms. It inhibits the enzyme carbonic anhydrase, which is involved in hydration and the production of bicarbonate ions. 4-Hydroxymethylbenzenesulfonamide has been shown to be active against streptococci and cryptococcus neoformans, but not against bacteria such as Escherichia coli or Pseudomonas aeruginosa.</p>Formula:C7H9NO3SPurity:Min. 95%Molecular weight:187.22 g/mol1-Trityl-1H-imidazole-2-carboxaldehyde
CAS:<p>1-Trityl-1H-imidazole-2-carboxaldehyde is a formylating agent that inhibits tumor growth and has anti-proliferative effects. It binds to the c–h bond of imidazoles in human prostate cells and forms a stable, cell cycle-specific metabolite. This metabolite has been shown to inhibit tumor growth in vivo. 1-Trityl-1H-imidazole-2-carboxaldehyde may be useful as a chemotherapeutic agent for prostate cancer or other cancers with similar metabolic profiles.</p>Formula:C23H18N2OPurity:Min. 95%Molecular weight:338.41 g/mol2,2-Diethyl-1,3-dioxaindan-5-amine
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H15NO2Purity:Min. 95%Molecular weight:193.24 g/mol
