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238244

Sigma-Aldrich

Iodocyclohexane

98%

Synonym(s):

Cyclohexyl iodide

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About This Item

Empirical Formula (Hill Notation):
C6H11I
CAS Number:
626-62-0
Molecular Weight:
210.06
Beilstein/REAXYS Number:
1900797
EC Number:
210-957-8
MDL number:
MFCD00003826
UNSPSC Code:
12352100
PubChem Substance ID:
24854149
NACRES:
NA.22

Quality Level

100

assay

98%

form

liquid

contains

copper as stabilizer

refractive index

n20/D 1.5441 (lit.)

bp

80-81 °C/20 mmHg (lit.)

density

1.624 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

IC1CCCCC1

InChI

1S/C6H11I/c7-6-4-2-1-3-5-6/h6H,1-5H2

InChI key

FUCOMWZKWIEKRK-UHFFFAOYSA-N

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General description

The photodissociation dynamics of iodocyclohexane has been studied using velocity map imaging. Nickel catalyzed coupling of iodocyclohexane with 1-octyne has been investigated.

Application

Iodocyclohexane has been employed as reagent in demethylation of aryl methyl ethers in DMF under reflux condition.

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

158.0 °F - closed cup

flash_point_c

70 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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D K Zaouris et al.
The Journal of chemical physics, 135(9), 094312-094312 (2011-09-15)
The photodissociation dynamics of iodocyclohexane has been studied using velocity map imaging following excitation at many wavelengths within its A-band (230 ≤ λ ≤ 305 nm). This molecule exists in two conformations (axial and equatorial), and one aim of the
An efficient method for demethylation of aryl methyl ethers.
Zuo L, et al.
Tetrahedron Letters, 49(25), 4054-4056 (2008)
Jun Yi et al.
Angewandte Chemie (International ed. in English), 52(47), 12409-12413 (2013-10-12)
A nicked reaction: The title reaction of terminal alkynes with non-activated secondary alkyl iodides and bromides was accomplished for the first time. This reaction provides a new and practical approach for the synthesis of substituted alkynes (see scheme; cod=cyclo-1,5-octadiene).

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