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Trifluoromethyliodine(III) bis-trifluoroacetate, also known as CF3I(OCOCF3)2, is a chemical compound consisting of a trifluoromethyl group (CF3) bonded to an iodine(III) center, with two trifluoroacetate (OCOCF3) ligands. This organoiodine compound is a valuable reagent in organic synthesis, particularly for the introduction of the trifluoromethyl group into various organic molecules. It is known for its stability and reactivity, which makes it a useful intermediate in the preparation of trifluoromethylated compounds. These compounds are important due to their unique properties and applications in pharmaceuticals, agrochemicals, and materials science. Trifluoromethyliodine(III) bis-trifluoroacetate is typically synthesized through the reaction of trifluoroacetic acid with iodine(III) trifluoride and is handled with care due to its potential reactivity and toxicity.

60669-28-5

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60669-28-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60669-28-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,6,6 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 60669-28:
(7*6)+(6*0)+(5*6)+(4*6)+(3*9)+(2*2)+(1*8)=135
135 % 10 = 5
So 60669-28-5 is a valid CAS Registry Number.

60669-28-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Trifluoromethyliodine(III) bis-trifluoroacetate

1.2 Other means of identification

Product number -
Other names Trifluormethyliod-bis-trifluoracetat

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:60669-28-5 SDS

60669-28-5Relevant academic research and scientific papers

Polar trifluoromethylation reactions: the formation of bis(trifluoromethyl)iodine(III) compounds and trifluoromethyl iodine(III) cations and anions

Tyrra, Wieland,Naumann, Dieter

, p. 327 - 333 (2007/10/02)

IX3 (X = Cl, OCOCF3, ONO2) reacts with Cd(CF3)2 complexes or Bi(CF3)3 to yield the corresponding CF3IX2 derivatives. 19F nuclear magnetic resonance spectroscopic evidence is found for + and I(CF3)2X (X = Cl, OCOCF3) in the reactions of CF3IX2 with Cd(CF3)2 complexes.During the reaction of CF3IF2 and Hg(CF3)2 the new species I(CF3)2F and cis-- are identified by nuclear magnetic resonance spectroscopy.The reactions proceed under polar conditions and can be accelerated by the addition of a Lewis acid such as BF3, B(OCOCF3)3, or Sb(V) compounds.Difluoromethyl compounds are formed as by-products.Key words: polar trifluoromethylations, trifluoromethyl iodine(III) compounds, difluoromethyl group formation.

ON SOME NEW TRIFLUOROMETHYL IODINE(III) COMPOUNDS: REACTIONS OF CF3IF2 WITH BORON AND SILICON COMPOUNDS AND CF3ICl2 WITH SILVER SALTS

Tyrra, Wieland,Naumann, Dieter

, p. 401 - 416 (2007/10/02)

CF3IF2 undergoes fluorine exchange reactions with BX3 (X = Cl, Br, I, OCOCF3) to form the compounds CF3IX2.The reactions of CF3IF2 with (CF3)2BN(CH3)2, (CH3)3SiNCO and (CH3)3SiN(CH3)COCF3 yield the corresponding new trifluoromethyl iodine (III) nitrogen compounds.A preparative method for the synthesis of CF3ICl2 is found by reacting CF3IF2 with (CH3)3SiCl.CF3ICl2 reacts with AgX (X = OCOCF3, SCF3) to yield the corresponding CF3IX2 compounds and with (C6H5)4AsCl the novel ion (-) is detected.Products were identified by n.m.r. spectroscopy.

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