CAS 594-38-7
:2-Iodo-2-methylbutane
Description:
2-Iodo-2-methylbutane, with the CAS number 594-38-7, is an organic compound classified as a haloalkane. It features a branched structure, consisting of a butane backbone with an iodine atom and a methyl group attached to the second carbon. This compound is typically a colorless liquid at room temperature and is known for its relatively low boiling point compared to other haloalkanes. It is soluble in organic solvents but has limited solubility in water due to its hydrophobic nature. The presence of the iodine atom makes it a good candidate for nucleophilic substitution reactions, often serving as a precursor in organic synthesis. Additionally, 2-iodo-2-methylbutane can undergo elimination reactions, leading to the formation of alkenes. Its reactivity and structural characteristics make it useful in various chemical applications, including the synthesis of pharmaceuticals and agrochemicals. Safety precautions should be taken when handling this compound, as iodine-containing compounds can be hazardous.
Formula:C5H11I
InChI:InChI=1S/C5H11I/c1-4-5(2,3)6/h4H2,1-3H3
InChI key:InChIKey=NWRZTQFWFPLHHX-UHFFFAOYSA-N
SMILES:C(CC)(C)(C)I
Synonyms:- 1,1-Dimethyl-n-propyl iodide
- 2-Iodo-2-methylbutane
- Butane, 2-iodo-2-methyl-
- tert-Amyl iodide
- tert-Pentyl iodide
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2-Iodo-2-methylbutane
CAS:<p>2-Iodo-2-methylbutane (2IMB) is an organic compound that is used as a reagent in organic chemistry. It is an alkyne that has been shown to react with tellurium, forming a tetraalkyltetrahalide. This reaction can be observed by the addition of 2IMB to a solution containing tellurium and anions in a chromatographic method. The frequency range for this reaction is between 10 and 300 MHz. 2IMB has been shown to have two chiral centers, which means it can exist as four different stereoisomers. These four stereoisomers are:</p>Formula:C5H11IPurity:Min. 95%Molecular weight:198.05 g/mol
