626-62-0 | Iodocyclohexane, stab. with copper

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$16.00	$11.00
5g	98%	in stock	$18.00	$13.00
10g	98%	in stock	$20.00	$14.00
25g	98%	in stock	$33.00	$23.00
500g	98%	in stock	$547.00	$383.00

Description

• Catalog Number: AB74786
• Chemical Name: Iodocyclohexane, stab. with copper
• CAS Number: 626-62-0
• Molecular Formula: C6H11I
• Molecular Weight: 210.056
• MDL Number: MFCD00003826
• SMILES: IC1CCCCC1
• NSC Number: 6075

Computed Properties

• Complexity: 46.1
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 7
• XLogP3: 3.8

Upstream Synthesis Route

Iodocyclohexane is a versatile compound that finds widespread application in chemical synthesis as a valuable building block. Its unique structure, consisting of a cyclohexane ring with an iodine atom attached, makes it a valuable reagent for various reactions in organic chemistry. One of the key applications of iodocyclohexane is in the halogenation of organic compounds. The iodine atom in the molecule can be easily substituted with other functional groups, allowing for the introduction of new chemical functionalities into a molecule. This property makes iodocyclohexane a valuable tool for the synthesis of complex organic molecules and pharmaceutical intermediates.Furthermore, iodocyclohexane can also participate in radical reactions, serving as a radical initiator or a radical acceptor. This property enables its use in radical halogenation, radical cyclization, and other radical-mediated transformations, making it a versatile reagent in the toolbox of synthetic chemists. Overall, the strategic placement of the iodine atom on the cyclohexane ring confers unique reactivity to iodocyclohexane, making it a valuable reagent for various chemical transformations in organic synthesis.

Literature

• Conformer specific dissociation dynamics of iodocyclohexane studied by velocity map imaging.

  The Journal of chemical physics 20110907

• Subtle factors are important: radical formation and transmetallation in reactions of butyl cuprates with cyclohexyl iodide.

  Organic & biomolecular chemistry 20050207

• Evidence for a NiI active species in the catalytic cross-coupling of alkyl electrophiles.

  Journal of the American Chemical Society 20040707