CAS 53750-52-0

4-Iodo-2-methyl-1-butene

Description:

4-Iodo-2-methyl-1-butene is an organic compound characterized by its structure, which includes a butene backbone with a methyl group and an iodine substituent. It is classified as an alkene due to the presence of a carbon-carbon double bond. The compound has a molecular formula that reflects its composition of carbon, hydrogen, and iodine atoms. Its physical properties typically include a low boiling point and moderate solubility in organic solvents, which is common for alkenes. The presence of the iodine atom can impart unique reactivity, making it a useful intermediate in organic synthesis, particularly in reactions such as nucleophilic substitutions or coupling reactions. Additionally, the compound may exhibit specific optical properties due to the arrangement of its substituents. Safety considerations should be taken into account when handling this substance, as iodine can be hazardous, and proper laboratory protocols should be followed. Overall, 4-Iodo-2-methyl-1-butene is a valuable compound in synthetic organic chemistry.

Formula: C₅H₉I

InChI: InChI=1S/C5H9I/c1-5(2)3-4-6/h1,3-4H2,2H3

InChI key: InChIKey=WOMUECWVNKNZEP-UHFFFAOYSA-N

SMILES: C(C(C)=C)CI

Synonyms:

• 3-Methyl-3-butenyl iodide
• 1-Butene, 4-iodo-2-methyl-
• 1-Iodo-3-methyl-3-butene
• 4-Iodo-2-methyl-1-butene

4-Iodo-2-methyl-1-butene

Controlled Product

CAS: 53750-52-0

Applications 4-Iodo-2-methyl-1-butene is an reagent used in the synthesis of functionalized cyclic boronates.
References Altenhofer, E., et al.: Org. Lett., 16, 3 (2014);

Formula: C₅H₉I

Color and Shape: Neat

Molecular weight: 196.03

Ref: TR-I708590

4-Iodo-2-methylbut-1-ene

CAS: 53750-52-0

4-Iodo-2-methylbut-1-ene is an alkylating agent that forms a covalent bond with DNA. It can be synthesized by the reaction of an electrophile, such as methyl iodide, with an enone. This process is stereoselective and stereoselectively mediated. The compound is used in the synthesis of pheromones and has been shown to have cytotoxic effects on tumor cells. 4-Iodo-2-methylbut-1-ene can be synthesized by the catalysis of trifluoromethanesulphonate. When this reagent reacts with an organic molecule containing a reactive group, it forms a covalent bond with DNA and inhibits protein synthesis.

Formula: C₅H₉I

Purity: Min. 95%

Molecular weight: 196.03 g/mol

Ref: 3D-DCA75052