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2253-02-3

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2253-02-3 Usage

Physical State

Colorless, flammable gas

Molecular Structure

Cyclobutane with five fluorine atoms

Primary Use

Refrigerant in air conditioning and refrigeration systems

Environmental Impact

Low global warming potential and ozone depletion potential

Environmental Advantage

More environmentally friendly alternative to other refrigerants

Thermal Stability

High thermal stability

Toxicity

Non-toxic

Industrial Applications

Safe for use in various industrial applications

Replacement

Widespread use as a replacement for older, more harmful refrigerants

Check Digit Verification of cas no

The CAS Registry Mumber 2253-02-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,5 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2253-02:
(6*2)+(5*2)+(4*5)+(3*3)+(2*0)+(1*2)=53
53 % 10 = 3
So 2253-02-3 is a valid CAS Registry Number.
InChI:InChI=1/C4H3F5/c5-2-1-3(6,7)4(2,8)9/h2H,1H2

2253-02-3SDS

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 1,1,2,2,3-PENTAFLUOROCYCLOBUTANE

1.2 Other means of identification

Product number -
Other names 3H,4H,4H-Perfluorocyclobutane

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:2253-02-3 SDS

2253-02-3Downstream Products

2253-02-3Relevant articles and documents

METHOD FOR PRODUCING HYDROGEN-CONTAINING FLUOROOLEFIN COMPOUND

-

Page/Page column 5, (2011/04/18)

An unsaturated hydrogen-containing fluoroolefin compound is obtained by bringing an unsaturated fluorine-containing halogen compound into contact with 0.1 to 3 molar equivalents of hydrogen relative to the unsaturated fluorine-containing halogen compound in a vapor phase in the presence of a supported palladium catalyst in which an amount of supported palladium is 0.1% by weight to 2.5% by weight.

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