3D-FC42373 - 6-chloroimidazo12-apyrazine
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2-Phenyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyrazine
CAS:Formula:C12H13N3Purity:95%Color and Shape:SolidMolecular weight:199.2517Hexahydropyrrolo[1,2-a]pyrazin-4(1H)-one hydrochloride
CAS:Formula:C7H13ClN2OMolecular weight:176.64393-(Trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazine, HCl
CAS:Formula:C6H8ClF3N4Purity:97%Color and Shape:SolidMolecular weight:228.60273-Phenyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyrazine
CAS:Formula:C12H13N3Purity:97%Color and Shape:SolidMolecular weight:199.2517[1,2,4]Triazolo[1,5-a]pyrazin-2-amine
CAS:Formula:C5H5N5Purity:97%Color and Shape:SolidMolecular weight:135.1267HEXAHYDRO-PYRROLO[1,2-A]PYRAZIN-6-ONE HYDROCHLORIDE
CAS:Formula:C7H13ClN2OPurity:97%Color and Shape:SolidMolecular weight:176.64394-OXO-4,5,6,7-TETRAHYDROPYRAZOLO[1,5-A] PYRAZINE-2-CARBOXYLIC ACID
CAS:Formula:C7H7N3O3Purity:98%Color and Shape:SolidMolecular weight:181.14883-Bromo-5,6,7,8-tetrahydroimidazo[1,2-a]pyrazine dihydrochloride
CAS:Formula:C6H10BrCl2N3Molecular weight:274.9737(R)-octahydro-pyrido[1,2-a]pyrazine dihydrochloride
CAS:Formula:C8H18Cl2N2Purity:97%Color and Shape:SolidMolecular weight:213.14794,5,6,7-tetrahydro-4-oxo-Pyrazolo[1,5-a]pyrazine-2-carboxylic acid methyl ester
CAS:Formula:C8H9N3O3Purity:97%Molecular weight:195.17542-Methyl-5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyrazine
CAS:Formula:C6H10N4Purity:98%Color and Shape:SolidMolecular weight:138.1704Ethyl 5,6,7,8-tetrahydroimidazo[1,2-a]pyrazine-2-carboxylate hydrochloride
CAS:Formula:C9H14ClN3O2Purity:97%Color and Shape:SolidMolecular weight:231.67945H-5-Methyl-6,7-dihydrocyclopentapyrazine
CAS:Formula:C8H10N2Purity:>97.0%(GC)(T)Color and Shape:Colorless to Light yellow to Light orange clear liquidMolecular weight:134.182-Methyl-6,7-dihydro-5H-cyclopentapyrazine
CAS:Formula:C8H10N2Color and Shape:NeatMolecular weight:134.182-Cyanopyrazine
CAS:2-Cyanopyrazine is a molecule that belongs to the group of nitrogen-containing heterocyclic compounds. It has been shown to exhibit antiinflammatory activity in skin cancer cells and bacterial strain, group P2. This compound inhibits the growth of bacteria by binding to their pyrazinoic acid, which is an electron acceptor. 2-Cyanopyrazine also exhibits tuberculostatic activity against M. tuberculosis and M. avium complex by inhibiting the synthesis of mycolic acids and cell wall lipids, respectively. The redox cycle of this compound is coordinated with a hydrogen bond between the hydroxyl group and the carbonyl carbon atom. 2-Cyanopyrazine is oxidized from its initial state through a reaction mechanism involving molecular oxygen or hydrogen peroxide as an oxidant and water as a reductant. The oxidation products can be reduced back to 2-cyanoapyrazine using ascorbate or NADH asFormula:C5H3N3Purity:Min. 95%Color and Shape:Off-White To Light (Or Pale) Yellow Solid Or Liquid (May Vary)Molecular weight:105.1 g/molOctahydro-1H-Cyclopentapyrazine-1-carboxylic Acid 1,1-Dimethylethyl Ester
CAS:Controlled ProductFormula:C12H22N2O2Color and Shape:NeatMolecular weight:226.32(4aR,7aS)-Rel-octahydro-cyclopentapyrazine-1-carboxylic acid tert-butyl ester
CAS:Versatile small molecule scaffoldFormula:C12H22N2O2Purity:Min. 95%Molecular weight:226.32 g/mol




