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Merck
CN

794473

Ritter Trifluoroiodomethane-TMG Reagent

Synonym(s):

TMG-CF3I, Tetramethylguanidine-trifluoromethyl iodide adduct

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About This Item

Empirical Formula (Hill Notation):
C6H13F3IN3
Molecular Weight:
311.09
MDL number:
UNSPSC Code:
12352101
PubChem Substance ID:
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form

liquid

Quality Level

reaction suitability

reaction type: C-C Bond Formation

refractive index

n/D 1.461

density

1.495 g/mL at 25 °C

functional group

amine, fluoro, iodo

shipped in

dry ice

storage temp.

2-8°C

SMILES string

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

InChI

1S/C5H13N3.CF3I/c1-7(2)5(6)8(3)4;2-1(3,4)5/h6H,1-4H3;

InChI key

KIOFDNCUJQQUCD-UHFFFAOYSA-N

Application

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


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

No data available

flash_point_c

No data available

Regulatory Information

新产品

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Related Content

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.





Global Trade Item Number

SKUGTIN
794473-5ML04061838085559