Allyl iodide (3-iodopropene) is an organic halide used in synthesis of other organic compounds such as N-alkyl-2-pyrrolidones, [1] [failed verification] sorbic acid esters, [1] 5,5-disubstituted barbituric acids, [2] [failed verification] and organometallic catalysts.

Allyl iodide | C3H5I | CID 11166 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.

Allyl iodide 98%; CAS Number: 556-56-9; EC Number: 209-130-4; Synonyms: 3-Iodo-1-propene; Linear Formula: CH2=CHCH2I at Sigma-Aldrich

ALLYL IODIDE is moderately reactive. Incompatible with strong oxidizing and reducing agents. Also, incompatible with many amines, nitrides, azo/diazo compounds, alkali metals, and epoxides.

Monograph ID M1555 Title Allyl Iodide UNII 46830QOA4D Molecular formula C 3 H 5 I Molecular weight 167.98 Percent composition C 21.45%, H 3.00%, I 75.55% Standard InChI

The thermochemistry of the isomerization of 3-halopropenes (allyl halides) to 1-halopropenes; entropy and enthalpy of formation contribution of the Cd- (H) (X) group, J. Chem. Thermodyn., 1973, 5, 411-420. [all data] Go To: Top, Reaction thermochemistry data, References.

Allyl iodide (3-iodopropene) is an organic halide used in synthesis of other organic compounds such as N-alkyl-2-pyrrolidones, sorbic acid esters, 5,5-disubstituted barbituric acids, and organometallic catalysts.

Allyl iodide (3-iodopropene) is an organic halide used in synthesis of other organic compounds such as N-alkyl-2-pyrrolidones, [1] [failed verification] sorbic acid esters, [1] 5,5-disubstituted barbituric acids, [2] [failed verification] and organometallic catalysts.