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91987

Sigma-Aldrich

1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10-Henicosafluoro-12-iodododecane

≥95.0% (GC)

Synonym(s):

1-Iodo-1H,1H,2H,2H-perfluorododecane, 1H,1H,2H,2H-Perfluorododecyl iodide

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About This Item

Linear Formula:
CF3(CF2)9CH2CH2I
CAS Number:
2043-54-1
Molecular Weight:
674.03
Beilstein:
1897869
EC Number:
218-054-0
MDL number:
MFCD00039412
UNSPSC Code:
12352200
PubChem Substance ID:
57653463
NACRES:
NA.22

Assay

≥95.0% (GC)

form

powder

SMILES string

FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)CCI

InChI

1S/C12H4F21I/c13-3(14,1-2-34)4(15,16)5(17,18)6(19,20)7(21,22)8(23,24)9(25,26)10(27,28)11(29,30)12(31,32)33/h1-2H2

InChI key

HVWXRMINOYZYCK-UHFFFAOYSA-N

Other Notes

Building block to introduce a fluorinated "pony tail" in compounds for fluorous phase «immobilization» by fluorous phase partition

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

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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Wilson et al.
The Journal of organic chemistry, 65(9), 2619-2623 (2000-05-16)
Fullerene (C60) Diels-Alder adducts with perfluoroalkylated 1,3-cyclopentadiene (1a,b) were synthesized and studied. The perfluoroalkylated cyclopentadiene was found to be less reactive toward C60 than cyclopentadiene itself, possibly because of the electron-withdrawing effect of the side chain. Because of the same
Armido Studer et al.
The Journal of organic chemistry, 62(9), 2917-2924 (1997-05-02)
A new protocol for multicomponent condensation reactions that uses fluorous (highly fluorinated) substrates is introduced. This method takes advantage of the ease of purification of fluorous compounds by liquid-liquid extractions between fluorous and organic solvents. The application of this method
R.P. Hughes, H.A. Trujillo
Organometallics, 15, 286-286 (1996)
Daniel Rauber et al.
Physical chemistry chemical physics : PCCP, 19(40), 27251-27258 (2017-10-11)
Ionic liquids (ILs) exhibit tunable behaviour and properties that are due to their supramolecular structure. We synthesized a series of alkylated and fluorinated phosphonium dicyanamide ILs to study the relation between molecular structure and assembly with a focus on the

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