Iodoform

2-Iodobutane was degraded by reductive dehalogenation with nickel-aluminum alloy in potassium hydroxide solution . The release rate of 2-iodobutane, a volatile organoiodide, was studied .

2-Iodobutane was degraded by reductive dehalogenation with nickel-aluminum alloy in potassium hydroxide solution . The release rate of 2-iodobutane, a volatile organoiodide, was studied .

CH₃CHICH₂CH₃ CAS#: 513-48-4 F.W.: 184.02 sec-Butyl iodide. Stored over copper.

CH₃CHICH₂CH₃ CAS#: 513-48-4 F.W.: 184.02 sec-Butyl iodide. Stored over copper.

The standard molar enthalpy of 2-iodoethanol formation has been studied . Application 2-Iodoethanol was used in the synthesis of the neuroexcitants 3-(carboxymethyl)pyrrolidine-2,4-dicarboxylic acid, &#945-kainic acid, alpha-isokainic acid and

The standard molar enthalpy of 2-iodoethanol formation has been studied . Application 2-Iodoethanol was used in the synthesis of the neuroexcitants 3-(carboxymethyl)pyrrolidine-2,4-dicarboxylic acid, &#945-kainic acid, alpha-isokainic acid and

2-Iodonaphthalene

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

2-Iodophenylacetic acid is a substituted acetic acid that can be prepared from 2-iodobenzyl cyanide. It undergoes palladium-catalyzed reaction with allenes to form 1,3-butadienes.

2-Iodophenylacetic acid is a substituted acetic acid that can be prepared from 2-iodobenzyl cyanide. It undergoes palladium-catalyzed reaction with allenes to form 1,3-butadienes.

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2-Iodopropane is an organ iodine compound. It is commonly used as a homolytic and heterolytic alkylating agent and in the preparation of the &#945-isopropoxymethylene blocking group.