
Heterocycles with Oxygen (O)
Heterocycles with oxygen atoms are a class of organic compounds where one or more oxygen atoms are part of the ring structure. These compounds are essential in the synthesis of pharmaceuticals, agrochemicals, and materials due to their unique reactivity and stability. Oxygen-containing heterocycles are used in various applications, including drug development and polymer science. At CymitQuimica, we offer a wide range of high-quality oxygen-containing heterocycles to support your research and industrial needs.
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5,6-Dimethoxy-7-nitro-2-benzofuran-1(3H)-one
CAS:Please enquire for more information about 5,6-Dimethoxy-7-nitro-2-benzofuran-1(3H)-one including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormula:C10H9NO6Purity:Min. 95%Molecular weight:239.18 g/mol1,4-DIOXA-SPIRO[4.5]DECAN-8-OL
CAS:Formula:C8H14O3Purity:98%Color and Shape:LiquidMolecular weight:158.1955-Boronofuran-2-carboxylic acid
CAS:Formula:C5H5BO5Purity:96%Color and Shape:SolidMolecular weight:155.9012α-D-Mannofuranose, 2,3:5,6-bis-O-(1-methylethylidene)-
CAS:Formula:C12H20O6Purity:98%Color and Shape:SolidMolecular weight:260.2836(1R,2S)-rel-2-(2,3-Dihydro-4-benzofuranyl)-cyclopropanemethanamine
CAS:Controlled ProductFormula:C12H15NOColor and Shape:NeatMolecular weight:189.2544-Amino-6-bromo-5-cyano-7-(2-β-C-methyl-2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-7H-pyrrolo[2.3-d]pyrimidine
Please enquire for more information about 4-Amino-6-bromo-5-cyano-7-(2-beta-C-methyl-2,3,5-tri-O-benzoyl-beta-D-ribofuranosyl)-7H-pyrrolo[2.3-d]pyrimidine including the price, delivery time and more detailed product information at the technical inquiry form on this pagePurity:Min. 95%3-Acetyl-2-ethylbenzofuran
CAS:Please enquire for more information about 3-Acetyl-2-ethylbenzofuran including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormula:C12H12O2Purity:Min. 95%Molecular weight:188.22 g/molFluoro 2-(5-Oxo-2H-Furan-2-Yl)Acetate
CAS:Fluoro 2-(5-Oxo-2H-Furan-2-Yl)Acetate is a structural analog of fluoroacetate. It has been shown to be metabolized by microorganisms and produces a number of reaction products, including aromatic hydrocarbons. Fluoro 2-(5-Oxo-2H-Furan-2-Yl)Acetate binds to the enzyme p450 and inhibits its activity, which may lead to drug toxicity. This compound has also been shown to inhibit amino acid synthesis and enzyme activities in staphylococcus aureus. Fluoro 2-(5-Oxo-2H-Furan-2-Yl)Acetate has an optimal pH level of 8 and is active against bacteria that grow at this pH range.Formula:C6H5FO4Purity:Min. 95%Molecular weight:160.1 g/mol3,4-Dimethylfuran
CAS:Stability Volatile Applications 3,4-Dimethylfuran (cas# 20843-07-6) is a compound useful in organic synthesis. Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the packageFormula:C6H8OColor and Shape:NeatMolecular weight:96.136-BROMO-1,4-BENZODIOXANE
CAS:Formula:C8H7BrO2Purity:97%Color and Shape:LiquidMolecular weight:215.0442-ETHOXY-3,4-DIHYDRO-2H-PYRAN
CAS:Formula:C7H12O2Purity:97%Color and Shape:LiquidMolecular weight:128.16898(2Z)-6-Hydroxy-2-(3-methoxybenzylidene)-7-methyl-1-benzofuran-3(2H)-one
CAS:Please enquire for more information about (2Z)-6-Hydroxy-2-(3-methoxybenzylidene)-7-methyl-1-benzofuran-3(2H)-one including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormula:C17H14O4Purity:Min. 95%Molecular weight:282.29 g/molRef: 3D-FH126422
Discontinued product3,5-Di-O-(tert-butyldimethylsilyl)-2-deoxy-D-ribono-1,4-lactone
CAS:Formula:C17H36O4Si2Purity:95%Color and Shape:SolidMolecular weight:360.63635-HYDROXY-1-BENZOFURAN-2-CARBOXYLIC ACID
CAS:Formula:C9H6O4Purity:95%Color and Shape:SolidMolecular weight:178.1415Benzofuran-3-ylboronic acid
CAS:Formula:C8H7BO3Purity:98%Color and Shape:SolidMolecular weight:161.9504N-[(8-Fluoro-2,3-Dihydro-1-Methyl-5-Phenyl-1H-1,4-Benzodiazepin-2-Yl)Methyl]-3-Furancarboxamide
CAS:Controlled ProductN-[(8-Fluoro-2,3-Dihydro-1-Methyl-5-Phenyl-1H-1,4-Benzodiazepin-2-Yl)Methyl]-3-Furancarboxamide is a hydrophobic, implanting drug with an iontophoresis device. It has been shown to have therapeutic effects in cancer. The drug is a targetable molecule that can be used for diagnostic purposes and the treatment of various cancers. N-[(8-Fluoro-2,3-Dihydro-1,5 -Phenyl 1H -1,4 Benzodiazepin 2 Yl) Methyl] 3 Furancarboxamide has been shown to inhibit cell proliferation by blocking the synthesis of proteins required for DNA replication and also inhibits the activity of protein kinase C.Purity:Min. 95%Benzofuran-7-carboxylic acid
CAS:Benzofuran-7-carboxylic acid is a growth factor that stimulates the release of human growth hormone. It also has been shown to stimulate the release of tryptophan and 5-hydroxytryptamine in humans. Benzofuran-7-carboxylic acid binds to receptors on gland cells, leading to increased production of peptide hormones such as ACTH. This compound can be used diagnostically for detecting the levels of camp in humans or other animals, or as a diagnostic agent for identifying human pathogens.Formula:C9H6O3Purity:Min. 95%Molecular weight:162.14 g/molRef: 3D-FB170547
Discontinued product2-Methyl-N-methyltetrahydro-2-furanmethanamine
CAS:Please enquire for more information about 2-Methyl-N-methyltetrahydro-2-furanmethanamine including the price, delivery time and more detailed product information at the technical inquiry form on this pagePurity:Min. 95%[(1S,3S)-3-[[4-Methoxy-3-(3-methoxypropoxy)phenyl]methyl]-4-methyl-1-[(2S, 4S)-tetrahydro-4-(1-methylethyl)-5-oxo-2-furanyl]pentyl]c arbamic acid 1,1-tert-butyl ester
CAS:[(1S,3S)-3-[[4-Methoxy-3-(3-methoxypropoxy)phenyl]methyl]-4-methyl-1-[(2S, 4S)-tetrahydro-4-(1-methylethyl)-5-oxo-2-furanyl]pentyl]car bamic acid 1,1-tert-butyl ester is a chiral building block that has been used in the scalable synthesis of various pharmaceuticals. The synthesis begins with ammonolysis of an amino chloride and chloroacetate. This reaction is followed by acetate extraction to yield the desired product. This process can be optimized by ring opening, magnesium removal and alkylation of aromatic hydrocarbons. The final reaction is the Suzuki coupling reaction with chromatographic purification.Formula:C30H49NO7Purity:Min. 95%Molecular weight:535.71 g/mol