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(1,243 products)
- Hydrocarbon Building Blocks(6,098 products)
- Organic Building Blocks(61,057 products)
Found 200716 products of "Building Blocks"
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4-benzoyloxane
CAS:<p>Versatile small molecule scaffold</p>Formula:C12H14O2Purity:Min. 95%Molecular weight:190.23 g/molN-Methyl-1-(1-methylpiperidin-3-yl)methanamine
CAS:<p>Versatile small molecule scaffold</p>Formula:C8H18N2Purity:Min. 95%Molecular weight:142.25 g/mol3-Methoxy-2,4-dimethylaniline
CAS:Versatile small molecule scaffoldFormula:C9H13NOPurity:Min. 95%Molecular weight:151.21 g/mol2-(2-Amino-2-phenylethoxy)-1,3-dimethylbenzene
CAS:2-(2-Amino-2-phenylethoxy)-1,3-dimethylbenzene is a molecule that binds to the sodium channel of nerve cells and blocks the flow of ions. It prevents the nerve cell from transmitting its signal. This drug has been shown to be effective in animal models for muscle spasms, but it is not used clinically because it can cause paralysis.Formula:C16H19NOPurity:Min. 95%Molecular weight:241.33 g/mol2-Phenylcycloheptan-1-one
CAS:<p>2-Phenylcycloheptan-1-one is a chemical used in organic synthesis. It has been shown to undergo decarbonylation and dimerization reactions, as well as rearrangements of the carbon-carbon double bond. These reactions are used to synthesize a wide variety of other molecules. The efficiency of 2-phenylcycloheptan-1-one depends on the type and amount of reagents used in the process, as well as on the structure of the molecule being synthesized. 2-Phenylcycloheptan-1-one is often used as a sensitizer for photochemical reactions due to its ability to absorb ultraviolet light.</p>Formula:C13H16OPurity:Min. 95%Molecular weight:188.26 g/molMethyl 3-methyl-5-oxohexanoate
CAS:<p>Versatile small molecule scaffold</p>Formula:C8H14O3Purity:Min. 95%Molecular weight:158.19 g/molN,6-Dimethylpyridazin-3-amine
CAS:Versatile small molecule scaffoldFormula:C6H9N3Purity:Min. 95%Molecular weight:123.16 g/mol1-Cyclopentyl-2-methoxyethan-1-one
CAS:<p>Versatile small molecule scaffold</p>Formula:C8H14O2Purity:Min. 95%Molecular weight:142.2 g/mol3-(5-Bromo-2-methylphenyl)propanoic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H11BrO2Purity:Min. 95%Molecular weight:243.1 g/mol2-Chloro-5-methylbenzaldehyde
CAS:<p>Versatile small molecule scaffold</p>Formula:C8H7ClOPurity:Min. 95%Molecular weight:154.59 g/mol4-Methoxyisobenzofuran-1,3-dione
CAS:<p>4-Methoxyisobenzofuran-1,3-dione is a natural product that belongs to the group of hydroxybenzoic acids. It is obtained by the hydrogenation of 3-nitrophthalic anhydride and 3-hydroxyphthalic anhydride, which are obtained from anacardic acid. 4-Methoxyisobenzofuran-1,3-dione has been used as an intermediate for antibiotics and synthetic dyestuffs. The chloride salt of this compound has been used as a reagent in organic synthesis.</p>Formula:C9H6O4Purity:Min. 95%Molecular weight:178.14 g/mol4-Amino-4'-hydroxybenzophenone
CAS:4-Amino-4'-hydroxybenzophenone is a benzophenone with a hydroxyl group in the ortho position. It has absorption spectra that are similar to those of benzene, but it is less soluble in solvents and more soluble in water. The molecule has two possible conformations, both of which have an equilibrium constant (K) of 10. The two conformations can interconvert by rotation about the C=C bond, which is referred to as torsion. This conformational change in the molecule alters its light absorption properties.Formula:C13H11NO2Purity:Min. 95%Molecular weight:213.24 g/mol4-(4-Phenylpiperazin-1-yl)benzoic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C17H18N2O2Purity:Min. 95%Molecular weight:282.34 g/mol2,3,4,5-Tetrahydro-1,4-benzothiazepine hydrochloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H12ClNSPurity:Min. 95%Molecular weight:201.72 g/mol2-Chloro-N-(4-methylbenzenesulfonyl)acetamide
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H10ClNO3SPurity:Min. 95%Molecular weight:247.7 g/mol2-Iodo-4-oxatricyclo[4.2.1.0,3,7]nonan-5-one
CAS:<p>Versatile small molecule scaffold</p>Formula:C8H9IO2Purity:Min. 95%Molecular weight:264.06 g/mol1-[Amino(methylsulfanyl)methylidene]guanidine hydroiodide
CAS:<p>Versatile small molecule scaffold</p>Formula:C3H9IN4SPurity:Min. 95%Molecular weight:260.1 g/mol3-Methyl-1,2,3,4-tetrahydronaphthalen-1-one
CAS:<p>3-Methyl-1,2,3,4-tetrahydronaphthalen-1-one is a methylated natural product. It is synthesized by the metalation of 1,2,3,4-tetrahydronaphthalene with methyl iodide and zinc. This reaction proceeds in two steps: first the ortho hydrogen of 1,2,3,4-tetrahydronaphthalene is replaced by the methyl group and then the nitrogen atom is alkylated. The formation of 3-methyl-1,2,3,4-tetrahydronaphthalen-1-one can be explained by an S N 2 substitution reaction in which a hydrogen on the methyl group attacks the electron deficient carbon atom of 1,2,3,4 tetrahydronaphthalene. 3-Methyl-1,2,3 4 tetrahydronaphthalen 1 one has been shown to</p>Formula:C11H12OPurity:Min. 95%Molecular weight:160.21 g/mol2,3,4,5-Tetrahydro-1,4-benzothiazepin-5-one
CAS:<p>2,3,4,5-Tetrahydro-1,4-benzothiazepin-5-one is a crystalline dimer that has a seven membered ring and two hydrogen bonds. The conformation of the molecule is centrosymmetric and the crystal structure has been determined by X-ray diffraction.</p>Formula:C9H9NOSPurity:Min. 95%Molecular weight:179.24 g/mol2-[(2-Aminoethyl)sulfanyl]benzoic acid hydrochloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H11NO2SPurity:Min. 95%Molecular weight:197.26 g/mol
