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Methane, trifluoro(fluoromethoxy)-, also known as 1,1,1-trifluoro-N-(fluoromethoxy)methane or HFC-263fb, is a halogenated alkane with the chemical formula C2H3F5O. It is a colorless, volatile liquid with a low boiling point and is used as a refrigerant, blowing agent, and fire suppressant. HFC-263fb is a potent greenhouse gas with a high global warming potential, making it a subject of concern for its environmental impact. It is also a byproduct in the production of other fluorocarbons and is being researched for its potential use in various industrial applications.

2261-01-0

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2261-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2261-01-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,6 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2261-01:
(6*2)+(5*2)+(4*6)+(3*1)+(2*0)+(1*1)=50
50 % 10 = 0
So 2261-01-0 is a valid CAS Registry Number.

2261-01-0SDS

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 trifluoro(fluoromethoxy)methane

1.2 Other means of identification

Product number -
Other names tetrafluorodimethyl 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:2261-01-0 SDS

2261-01-0Upstream product

2261-01-0Downstream Products

2261-01-0Relevant academic research and scientific papers

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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