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Methane, oxybis[trifluoro-], also known as trifluoromethane diazonium tetrafluoroborate or CF3N2BF4, is a chemical compound consisting of a methane molecule with two trifluoromethyl groups attached to a central nitrogen atom, which is further connected to a tetrafluoroborate ion. Methane, oxybis[trifluoro- is a colorless, crystalline solid that is highly sensitive to heat, shock, and friction, making it potentially explosive. It is used as a reagent in organic synthesis, particularly in the preparation of fluorinated compounds, and is also employed in the production of certain pharmaceuticals and agrochemicals. Due to its hazardous nature, it requires careful handling and storage under controlled conditions.

1479-49-8

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1479-49-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1479-49-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,7 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1479-49:
(6*1)+(5*4)+(4*7)+(3*9)+(2*4)+(1*9)=98
98 % 10 = 8
So 1479-49-8 is a valid CAS Registry Number.

1479-49-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name trifluoro(trifluoromethoxy)methane

1.2 Other means of identification

Product number -
Other names trifluoromethyl ether

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:1479-49-8 SDS

1479-49-8Relevant academic research and scientific papers

PROCESS FOR PREPARING HIGH PURITY MONOCARBOXYLIC PERFLUOROPOLYETHERS

-

Page/Page column 8, (2009/05/28)

A process for preparing monocarboxylic perfluoropolyethers of formula: A-O-(RF)z-(CFY)t-C(O)OX (I) wherein: X is H, C1-C10 alkyl, or an aryl group; Y=F, CF3; t=1, 2 or 3; A is a C1-C4 perfluoroalkyl end group; z=0 or 1; RF is a perfluorooxyalkylene chain; having a number average molecular weight in the range 180-8,000; comprising the following steps: a) one or more distillations of perfluoropolyethers (PFPE) of formula T-O-(RF)z-T′ (II) wherein: z and RF are as above defined; T, T′, equal to or different from each other, are selected from acyl fluoride or carbonyl-containing functional end groups and non functional end groups to obtain one PFPE fraction of formula (II) wherein the difference between the minimum and the maximum molecular weight of the components is lower than or equal to 600; b) partial fluorination of the fraction obtained in a); c) esterification c1) and/or hydrolysis c2) of the mixture obtained in b); d) distillation of the product obtained in c2) or in c1).

Technology for the preparation of perfluoro-organic compounds

Moldavskii, Dmitrii D.,Bispen, Tatjana A.,Kaurova, Galina I.,Furin, Georgii G.

, p. 157 - 167 (2007/10/03)

Fluorination by elemental fluorine of fluorine-containing alkenes, alkanes, ethers and tertiary amines was investigated, aimed at obtaining the perfluorinated analogs. The factors affecting yield of the target compounds were studied. Elements of technology were elucidated.

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