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Key Documents

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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)

Sinónimos:

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

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About This Item

Fórmula lineal:
CF3(CF2)9CH2CH2I
Número de CAS:
2043-54-1
Peso molecular:
674.03
Beilstein/REAXYS Number:
1897869
EC Number:
218-054-0
MDL number:
MFCD00039412
UNSPSC Code:
12352200
PubChem Substance ID:
57653463
NACRES:
NA.22

Quality Level

100

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

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
BCCL8459
BCCK5713
BCCL2284
BCCJ7474
BCCC6517

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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
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
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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