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bromotrifluoroethene epoxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54577-33-2

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54577-33-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54577-33-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,5,7 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 54577-33:
(7*5)+(6*4)+(5*5)+(4*7)+(3*7)+(2*3)+(1*3)=142
142 % 10 = 2
So 54577-33-2 is a valid CAS Registry Number.

54577-33-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name bromotrifluoroethene epoxide

1.2 Other means of identification

Product number -
Other names Bromtrifluoroxiran

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:54577-33-2 SDS

54577-33-2Downstream Products

54577-33-2Relevant academic research and scientific papers

Formation of bromodifluoroacetyl fluoride, CF2BrC(O)F, in the thermal gas-phase oxidation of bromotrifluoroethene, CF2CFBr, initiated by trifluoromethylhypofluorite, CF3OF

Czarnowski, Joanna

, p. 736 - 739 (2006)

The oxidation of CF2CFBr by molecular O2, initiated by CF3OF, has been studied at 273, 253.5, 239 and 218 K. The initial pressure of CF3OF was varied between 0.9 and 2.4 Torr, that of CF2CFBr between 11.5 and 30.7 Torr and that of O2 between 42.5 and 100.7 Torr. The main product was CF2BrC(O)F (yields 81-95% based on the CF2CFBr consumed). Minor amounts of C(O)F2 and C(O)FBr and traces of bromotrifluoroethene epoxide were also formed. The reaction is a chain reaction with bromine atoms as chain carriers. Its basic steps are: the thermal generation of CF3O{radical dot} radical by abstraction of fluorine atom from CF3OF, chain initiation by addition of CF3O{radical dot} to the double bond of alkene, leading, in presence of O2, to the formation of bromine atom and chain propagation by the reaction of bromine atom with CF2CFBr, originating CF2BrCFBrO{radical dot} radical. The predominant fate of the latter is the bromine atom extrusion with C{single bond}C bond scission playing the minor role. The full mechanism is postulated.

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