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Acetyl bromide, trifluoro-, also known as trifluoroacetyl bromide or CF3COBr, is a colorless, volatile, and highly reactive chemical compound with the molecular formula C2HBrF3O. It is a derivative of acetyl bromide, where the hydrogen atoms are replaced by fluorine atoms. Acetyl bromide, trifluoro- is widely used as a reagent in organic synthesis, particularly for the preparation of trifluoroacetic acid derivatives and other trifluoromethyl-containing compounds. Due to its high reactivity, it is essential to handle it with caution, as it can cause severe irritation to the eyes, skin, and respiratory system, and may also be harmful if ingested or inhaled.

354-31-4

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354-31-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 354-31-4 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 354-31:
(5*3)+(4*5)+(3*4)+(2*3)+(1*1)=54
54 % 10 = 4
So 354-31-4 is a valid CAS Registry Number.

354-31-4SDS

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 bromide

1.2 Other means of identification

Product number -
Other names Acetyl bromide,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:354-31-4 SDS

354-31-4Relevant academic research and scientific papers

Gas-phase photodissociation of CF3C(O)Cl between 193 and 280 nm

McGillen, Max R.,Burkholder, James B.

, p. 189 - 194 (2015/10/12)

Product yields were measured in the 296 K photolysis of CF3C(O)Cl at 193, 248, 254, and 280 nm. Br2 was used as a radical scavenger to convert the primary CF3 and CF3CO radical photofragments into stable bromides, CF3Br and CF3C(O)Br, which were quantified along with CO and CF2O using infrared absorption. The stabilized CF3CO radical yield increased with increasing photolysis wavelength from 3Cl quantum yield was determined to be 0.001 at all wavelengths.

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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