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Acetyl iodide, trifluoro-, also known as trifluoroacetyl iodide or CF3COI, is a chemical compound with the molecular formula C2F3IO. It is a colorless, volatile, and highly reactive liquid that is soluble in organic solvents. Acetyl iodide, trifluoro- is an important reagent in organic synthesis, particularly in the preparation of trifluoroacetyl derivatives and as a selective acylating agent. Due to its reactivity, it is sensitive to moisture and must be handled with care under anhydrous conditions. Trifluoroacetyl iodide is used in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals, where the introduction of trifluoroacetyl groups can significantly alter the properties of the target molecules.

354-36-9

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354-36-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 354-36-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,5 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 354-36:
(5*3)+(4*5)+(3*4)+(2*3)+(1*6)=59
59 % 10 = 9
So 354-36-9 is a valid CAS Registry Number.

354-36-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,2-trifluoroacetyl iodide

1.2 Other means of identification

Product number -
Other names Acetyl iodide,trifluoro

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:354-36-9 SDS

354-36-9Relevant academic research and scientific papers

PROCESSES FOR PRODUCING TRIFLUOROIODOMETHANE AND TRIFLUOROACETYL IODIDE

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Paragraph 0102-0118, (2020/03/09)

The present disclosure provides a process for producing trifluoroiodomethane, the process comprising providing a reactant stream comprising hydrogen iodide and at least one trifluoroacetyl halide selected from the group consisting of trifluoroacetyl chloride, trifluoroacetyl fluoride, trifluoroacetyl bromide, and combinations thereof, reacting the reactant stream in the presence of a first catalyst at a first reaction temperature from about 25° C. to about 400° C. to produce an intermediate product stream comprising trifluoroacetyl iodide, and reacting the intermediate product stream in the presence of a second catalyst at a second reaction temperature from about 200° C. to about 600° C. to produce a final product stream comprising the trifluoroiodomethane.

PROCESSES FOR PRODUCING TRIFLUOROIODOMETHANE

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Paragraph 0053-0055, (2020/03/09)

The present disclosure provides a gas-phase process for producing trifluoroiodomethane, the process comprising providing a reactant stream comprising hydrogen iodide and trifluoroacetyl halide selected from the group consisting of trifluoroacetyl chloride, trifluoroacetyl fluoride, trifluoroacetyl bromide, and combinations thereof, and reacting the reactant stream in the presence of a catalyst at a temperature from about 200° C. to about 600° C. to produce a product stream comprising the trifluoroiodomethane.

Facile conversion of perfluoroacyl fluorides into other acyl halides

Fukaya, Haruhiko,Matsumoto, Tomonori,Hayashi, Eiji,Hayakawa, Yoshio,Abe, Takashi

, p. 915 - 920 (2007/10/03)

Nine perfluoroacyl fluorides underwent halogen exchange when treated with anhydrous lithium halides to give acyl chlorides, bromides and iodides in high yields. The temperature dependence of this reaction is described. In the reaction with perfluorodiacyl fluoride, the diacyl halides possessing different acyl halide-groups were also produced. Of the alkaline metal salts used halogen exchange was successful only with lithium salts because of the interaction between lithium and fluorine.

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