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2356-62-9

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2356-62-9 Usage

General Description

1,2,2,2-Tetrafluoroethyl trifluoromethyl ether, also known as sevoflurane, is a colorless, nonflammable, sweet-smelling chemical widely used in medical applications as an inhalation anesthetic. It has the robustness to maintain its stability when exposed to light and air. The chemical possesses a high boiling point and, due to its high fluorine content, has low potential to deplete ozone. Apart from its prevalent use in medical anesthesia, it is also extensively studied in research for its potential applications due to its unique properties. Contact with this volatile liquid is known to cause skin and eye irritation and possible harm through ingestion or inhalation.

Check Digit Verification of cas no

The CAS Registry Mumber 2356-62-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,5 and 6 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2356-62:
(6*2)+(5*3)+(4*5)+(3*6)+(2*6)+(1*2)=79
79 % 10 = 9
So 2356-62-9 is a valid CAS Registry Number.
InChI:InChI=1/C3HF7O/c4-1(2(5,6)7)11-3(8,9)10/h1H

2356-62-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,1,2-tetrafluoro-2-(trifluoromethoxy)ethane

1.2 Other means of identification

Product number -
Other names HFE 227

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:2356-62-9 SDS

2356-62-9Downstream Products

2356-62-9Relevant articles and documents

Relative Rate Constants for the Reactions of CF3OF with Olefins in Solution

Navarrini, W.,Russo, A.,Tortelli, V.

, p. 6441 - 6443 (2007/10/03)

The addition reactions of CF3OF to chloro fluoro olefins have been studied in solution at low temperature (-78, -105 deg C), and their relative rate constants have been determined using the kinetic approach of competition reactions.The reactivity and regio- and stereoselectivity are consistent with a free radical chain-propagating reaction in which the alkenes are attacked by the CF3O* radical generated by homolytic cleavage of the O-F bond in the CF3OF molecule.

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