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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:
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.)

functional group

iodo

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 Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

158.0 °F - closed cup

Flash Point(C)

70 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

238244-25G:4548173987026
238244-100G:4548173987019
238244-VAR:
238244-BULK:

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Certificates of Analysis (COA)

Lot/Batch Number
MKCR8468
MKCS6776
MKCQ1605
MKCP6018
MKCN7116

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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).
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)

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