Description
1-(3-Fluorophenyl)-2-nitroethene is a fluorinated nitroalkene research chemical offered at a minimum purity of 95 %, with CAS number 705-84-0 and the empirical formula C₈H₆FNO₂. The molar mass is 167,14 g/mol, consistent with a compact aromatic nitroethene scaffold useful in synthetic organic chemistry. The 3-fluorophenyl substitution pattern makes it relevant for studies involving fluorine-containing building blocks, Michael acceptors, and nitroolefin chemistry. Clear specification of CAS number, formula, and molar mass supports reproducible documentation in research notebooks and quality records. This compound is available from manufacturer Carl ROTH as part of its biochemicals and fine-chemicals offering for professional laboratory use. It is suited to academic and industrial groups working on fluorinated aromatics, nitroethene intermediates, and related synthetic pathways that require a defined, catalogue-grade starting material.
This article is part of Organic building blocks & synthesis reagents, in Organic chemicals & synthesis reagents.
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Questions about 1-(3-Fluorophenyl)-2-nitroethene, min. 95 %, 500 mg
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1-(3-Fluorophenyl)-2-nitroethene, min. 95 %, 500 mg is the article on this page. Luminix Health distributes Carl Roth for laboratory use. It sits in Organic building blocks & synthesis reagents, inside Organic chemicals & synthesis reagents, in Lab chemicals.
A building block is an organic molecule bought to become part of a larger one. The structure, the CAS number and the purity decide it. A 95 percent reagent and a 99.9 percent reagent of the same name leave different impurities in the product. The functional groups are the reason it was chosen.
An organic chemical is built on carbon. In this category it is a building block or a reagent for making another molecule: a starting material, a coupling agent, a polymer, a PEG. Purity is a specification of which impurities remain. The structure, the CAS number and the grade decide whether two bottles are the same substance. Structures and properties are on PubChem. Nomenclature is IUPAC. Classification follows ECHA and the CLP Regulation.
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