Iodoform

2-Iodo-2-methylpropane was degraded by reductive dehalogenation with nickel-aluminum alloy in potassium hydroxide solution .

2-Iodo-5-methylthiophene is a halogenated thiophene. Application 2-Iodo-5-methylthiophene may be used for the preparation of: methylbis[2-(5-methyl)thienyl]borane dimethyl-terthienyl 5,5&#8242-dimethy-2,2&#8242-bithienyl

Analysis Note Purity (HPLC, area%): &#8805 99 Assay (ex N): &#8805 98 Identity (IR-spectrum): passes test Colour (2.5&#8199%, water): &#8804 50 APHA Melting point: &gt91 Fe (Iron): &#8804 20 ppm Water (according to Karl Fischer): &#8804 3

Analysis Note Purity (HPLC, area%): &#8805 99 Assay (ex N): &#8805 98 Identity (IR-spectrum): passes test Colour (2.5&#8199%, water): &#8804 50 APHA Melting point: &gt91 Fe (Iron): &#8804 20 ppm Water (according to Karl Fischer): &#8804 3

Analysis Note Purity (HPLC, area%): &#8805 99 Assay (ex N): &#8805 98 Identity (IR-spectrum): passes test Colour (2.5&#8199%, water): &#8804 50 APHA Melting point: &gt91 Fe (Iron): &#8804 20 ppm Water (according to Karl Fischer): &#8804 3

Analysis Note Purity (HPLC, area%): &#8805 99 Assay (ex N): &#8805 98 Identity (IR-spectrum): passes test Colour (2.5&#8199%, water): &#8804 50 APHA Melting point: &gt91 Fe (Iron): &#8804 20 ppm Water (according to Karl Fischer): &#8804 3

2-Iodoadenosine

2-Iodoadenosine

2-Iodoaniline is an aromatic amine that can be carbonylated to produce pentacyclic compounds.

2-Iodoaniline is an aromatic amine that can be carbonylated to produce pentacyclic compounds.

2-Iodoanisole participates in palladium catalyzed enantioselective Heck arylation of 2,3-dihydrofuran in the presence of chiral ionic liquids containing L-prolinate and L-lactate anions and non-chiral quaternary ammonium cations . Application

2-Iodoanisole participates in palladium catalyzed enantioselective Heck arylation of 2,3-dihydrofuran in the presence of chiral ionic liquids containing L-prolinate and L-lactate anions and non-chiral quaternary ammonium cations . Application