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794465

Sigma-Aldrich

Ritter Pentafluoroiodoethane-TMG Reagent

Synonym(s):

TMG-CF3CF2I, Tetramethylguanidine-pentafluoroethyl iodide adduct

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About This Item

Empirical Formula (Hill Notation):
C7H13F5IN3
Molecular Weight:
361.09
UNSPSC Code:
12352101
PubChem Substance ID:
NACRES:
NA.22

form

liquid

Quality Level

reaction suitability

reaction type: C-C Bond Formation

density

1.53 g/mL

functional group

amine
fluoro
iodo

shipped in

dry ice

storage temp.

2-8°C

SMILES string

FC(F)(F)C(F)(F)I.N=C(N(C)C)N(C)C

InChI

1S/C5H13N3.C2F5I/c1-7(2)5(6)8(3)4;3-1(4,5)2(6,7)8/h6H,1-4H3;

InChI key

ZFIASFCSDAHOLE-UHFFFAOYSA-N

Application

Product is a more convenient, liquified version of pentafluoroiodoethane, which can be utilized in photocatalytic and electrophilic pentafluoroethylation of olefins and heteroatoms respectively.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

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


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The Ritter lab currently focuses on fluorination chemistry for late-stage functionalization of complex natural and unnatural products. PhenoFluor™ has been developed as a general reagent for the selective, predictable, direct deoxyfluorination of complex alcohols and phenols.

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