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(6,093 products)
- Organic Building Blocks(60,525 products)
Found 195533 products of "Building Blocks"
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2-(Pyrrolidin-1-yl)pyridin-3-amine
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H13N3Purity:Min. 95%Molecular weight:163.22 g/molN2-Methylpyridine-2,3-diamine
CAS:<p>N2-Methylpyridine-2,3-diamine is a cytotoxic agent that is hydrophobic and has been shown to be cytotoxic against human cancer cells. It has been shown to inhibit protein synthesis in cancer cells by inhibiting the translation of mRNA into proteins.<br>N2-Methylpyridine-2,3-diamine inhibits the activity of diazepinones and other compounds that are involved in the synthesis of fatty acids and cholesterol. This compound also inhibits acetonitrile reductase, an enzyme involved in the synthesis of acetoacetate, which leads to cell death.</p>Formula:C6H9N3Purity:Min. 95%Molecular weight:123.16 g/mol1-Methyl-1H-imidazo[4,5-c]pyridine
CAS:<p>1-Methyl-1H-imidazo[4,5-c]pyridine is a heterocyclic compound with low yields and low yield. It has been used as an intermediate in the synthesis of other compounds. The major use of 1-methyl-1H-imidazo[4,5-c]pyridine is as a medicinal agent for the treatment of high blood pressure. The drug is taken orally or intravenously to reduce blood pressure by blocking the action of angiotensin II on vasculature. This drug also has antihypertensive effects due to its ability to inhibit xanthine oxidase and block sodium channels in vascular smooth muscle cells.</p>Formula:C7H7N3Purity:Min. 95%Molecular weight:133.15 g/mol(2Z)-2-Iodobut-2-enedioic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C4H3IO4Purity:Min. 95%Molecular weight:241.97 g/mol(2-Aminopropan-2-yl)phosphonic acid
CAS:<p>2-Aminopropan-2-yl)phosphonic acid is a natural product that has an orthorhombic crystal structure and a zwitterionic nature. It was first obtained in the form of a single-crystal x-ray diffraction pattern. It was found to have antibacterial activity against Marcescens, Valine, Esherichia coli, and other gram-positive bacteria. The molecule is also able to transport glutamic acid and valine across the cell membrane. The molecular structure consists of two aminopropyl groups attached to the phosphate group. One aminopropyl group has a carboxylic acid substituent and the other aminopropyl group has a phosphate substituent.</p>Formula:C3H10NO3PPurity:Min. 95%Molecular weight:139.09 g/mol3-(5-Methyl-1H-pyrazol-1-yl)propan-1-amine
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H13N3Purity:Min. 95%Molecular weight:139.2 g/molCyclododecanecarbaldehyde
CAS:<p>Cyclododecanecarbaldehyde is a reactive chemical that can be used for the epoxidation of octanes. It is an anti-inflammatory and it has been shown to have antifertility properties. Cyclododecanecarbaldehyde reacts with peracid to produce a high yield of epoxy tetronic solvents. This chemical also reacts with organoaluminium compounds to produce lactams, which are useful as introducing agents in the synthesis of cyclic compounds.</p>Formula:C13H24OPurity:Min. 95%Molecular weight:196.33 g/mol5,8-dimethyl-1,2,3,4-tetrahydronaphthalen-1-one
CAS:<p>5,8-dimethyl-1,2,3,4-tetrahydronaphthalen-1-one is a pyridinium compound with an aromatic ring. It has been shown to react with amines in the presence of a hydroxyl group to form pyrylium cations. 5,8-dimethyl-1,2,3,4-tetrahydronaphthalen-1-one is also capable of forming protonated and acetonitrile adducts. The activation energy for the reaction of 5,8-dimethyl-1,2,3,4-tetrahydronaphthalen-1-one with amines is very high (near 55 kcal/mol), which explains why this reaction does not occur spontaneously. This compound can be synthesized by irradiating naphthalene with deuterium radiation or cryogenic temperatures.</p>Formula:C12H14OPurity:Min. 95%Molecular weight:174.24 g/mol2-((2-(2-Hydroxyethoxy)ethyl)amino)ethan-1-ol
CAS:<p>Versatile small molecule scaffold</p>Formula:C6H15NO3Purity:Min. 95%Color and Shape:Clear LiquidMolecular weight:149.19 g/molBenzyl allylcarbamate
CAS:<p>Benzyl allylcarbamate is a potent inhibitor of enzymes. It is an inhibitor of the enzyme CYP2E1 and prevents the formation of reactive oxygen species (ROS) in cells. Benzyl allylcarbamate also has anti-inflammatory properties that are due to its ability to inhibit the production of pro-inflammatory cytokines such as tumor necrosis factor-α (TNF-α). This drug has been shown to be effective against atherosclerotic lesions in mice and congestive heart failure in rats. The biological properties of benzyl allylcarbamate have been studied extensively, including its effects on allergic responses and Alzheimer's disease.</p>Formula:C11H13NO2Purity:Min. 95%Molecular weight:191.23 g/molSodium 3,5-dichloro-4-methylbenzene-1-sulfonate
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H5Cl2NaO3SPurity:Min. 95%Molecular weight:263.07 g/mol(Phenylthio)propanone
CAS:<p>Phenylthiopropanone (PTPA) is an organic compound that belongs to the class of sulfoxides. It can be synthesized from ethyl ester, chloroform, and phenylthiol in a three-step process using methodologies such as biotransformations or chemoenzymatic reactions. PTPA can also be obtained by reacting sodium sulfoxide with phosphorus pentachloride. PTPA has been used as a precursor for other compounds including the hydroxy group, chloride, and synthetically desulfurized phenylthioacetaldehyde. The synthesis of PTPA is usually carried out in the presence of a catalyst and kinetic control of the reaction is necessary to avoid undesired side reactions.</p>Formula:C9H10OSPurity:Min. 95%Molecular weight:166.24 g/mol6-Chloro-2-naphthoic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H7ClO2Purity:Min. 95%Molecular weight:206.63 g/mol6-(Dimethylamino)-2-naphthoic acid
CAS:<p>6-(Dimethylamino)-2-naphthoic acid is a hydrophobic molecule that interacts with the cellular membrane. It has been shown to be an effective probe for studying the interactions of hydrophobic compounds with the lipid bilayer of cells. 6-(Dimethylamino)-2-naphthoic acid can be used as a fluorescent probe to measure levels of membrane phospholipids in cells. The fluorescence intensity is proportional to the number of molecules bound, and can be monitored by measuring changes in wavelength or lifetime. 6-(Dimethylamino)-2-naphthoic acid binds to nucleosides and thus has been used as a fluorescent probe for studying biological processes such as DNA replication, transcription, and translation.</p>Formula:C13H13NO2Purity:Min. 95%Molecular weight:215.25 g/mol7-Bromo-2-naphthalenecarboxylic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H7BrO2Purity:Min. 95%Molecular weight:251.08 g/mol8-Bromonaphthalene-2-carboxylic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H7BrO2Purity:Min. 95%Molecular weight:251.08 g/mol2,5-Dimethyl-1-(4-methylphenyl)-1H-pyrrole
CAS:<p>Versatile small molecule scaffold</p>Formula:C13H15NPurity:Min. 95%Molecular weight:185.26 g/mol1-(4-Bromophenyl)pyrrole
CAS:<p>1-(4-Bromophenyl)pyrrole is a primary amine that can be synthesized by cross-coupling of 1,2-dibromobenzene and pyrrole. This process involves the use of palladium as a catalyst to promote the reaction. The catalytic activity of the palladium is increased by hydrogen sulfate and chlorine, which act as promoters in this reaction. The synthesis of 1-(4-bromophenyl)pyrrole can also be accomplished by reacting with primary amines in tetrahydrofuran at high temperatures. Reaction conditions are also dependent on the presence or absence of fluorine gas, which may cause an increase in the yield and decrease in reaction time. In addition, irradiation can be used to break down pyrrole into its constituent parts for use in synthesizing 1-(4-bromophenyl)pyrrole.</p>Formula:C10H8BrNPurity:Min. 95%Molecular weight:222.08 g/mol4-Cyclopropylpyridine hydrochloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C8H10ClNPurity:Min. 95%Molecular weight:155.62 g/mol(4-Hydroxy-3,5-dimethoxyphenyl)methanaminium chloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H14ClNO3Purity:Min. 95%Molecular weight:219.66 g/mol
