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521582

Sigma-Aldrich

1-Chloro-6-iodohexane

96%

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About This Item

Linear Formula:
I(CH2)6Cl
CAS Number:
34683-73-3
Molecular Weight:
246.52
EC Number:
252-144-0
MDL number:
MFCD00039417
UNSPSC Code:
12352100
PubChem Substance ID:
24874214
NACRES:
NA.22

Quality Level

200

Assay

96%

refractive index

n20/D 1.5230 (lit.)

bp

110 °C (lit.)

density

1.623 g/mL at 25 °C (lit.)

functional group

chloro
iodo

SMILES string

ClCCCCCCI

InChI

1S/C6H12ClI/c7-5-3-1-2-4-6-8/h1-6H2

InChI key

QTJHNJCILMMRIQ-UHFFFAOYSA-N

General description

1-Chloro-6-iodohexane is an α,ω-dihaloalkane. 1,12-dichlorododecane is formed as a major product from the reduction of 1-chloro-6-iodohexane with nickel(I) salen. It affords 8-chloro-1-octyne on coupling with sodium acetylide.

Application

1-Chloro-6-iodohexane may be used in the preparation of 1,14-dichloro-7-tetradecyne and 10-2′-(methylphenyl)-7-decynyl chloride.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL5679
BCCG2292
BCCC2813
BCBV0954
BCBS2422V

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New synthesis of meromycolic acid.
Gensler WJ, et al.
The Journal of Organic Chemistry, 44(21), 3643-3652 (1979)
Synthesis of Methyl 11-(2'-Methylphenyl) undecanoate.
Michael WR.
Journal of Chemical and Engineering Data, 11(1), 134-135 (1996)
Homogeneous catalytic reduction of a, ?-dihaloalkanes with electrogenerated nickel (I) salen.
Mubarak MS and Peters DG.
Journal of Electroanalytical Chemistry, 388(1), 195-198 (1995)

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