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23228-89-9

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23228-89-9 Usage

General Description

Propane, 1,1,1,2,3,3,3-heptafluoro-2-(1,1,2,2-tetrafluoroethoxy)-, also known as HFO 1234ze, is a colorless, odorless, and non-toxic chemical compound. It is commonly used as a refrigerant in air conditioning and refrigeration systems, as well as a blowing agent in foam insulation. HFO 1234ze has a significantly lower global warming potential compared to traditional hydrofluorocarbon (HFC) refrigerants, making it a more environmentally friendly option. It also has good thermodynamic properties, which make it an effective alternative to HFCs in a variety of applications. Additionally, HFO 1234ze has a low ozone depletion potential, further contributing to its environmental benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 23228-89-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,2,2 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 23228-89:
(7*2)+(6*3)+(5*2)+(4*2)+(3*8)+(2*8)+(1*9)=99
99 % 10 = 9
So 23228-89-9 is a valid CAS Registry Number.

23228-89-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,1,2,3,3,3-heptafluoro-2-(1,1,2,2-tetrafluoroethoxy)propane

1.2 Other means of identification

Product number -
Other names -

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:23228-89-9 SDS

23228-89-9Downstream Products

23228-89-9Relevant articles and documents

PREPARATION OF SELECTED FLUOROOLEFINS

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Page 4, (2008/06/13)

A process is disclosed for producing (CF3)2C=CH2, CF3CH=CF2, CF2=C(CF3)OCF2CHF2 and C6H5C(CF3)=CF2. The process involves contacting the corresponding fluorocarbon starting material selected from (CF3)2CFCH2F, (CF3)2CHF, (CF3)2CFOCF2CHF2 and C6H5CF(CF3)2, in the vapor phase, with a defluorination reagent selected from carbon, copper, iron, nickel and zinc at an elevated temperature of at least 300 DEG C.

SYNTHESIS AND REACTIONS OF SOME PERFLUOROALKYL ETHER SUBSTITUTED SILANES

Chen, Grace J.,Tamborsky, Christ

, p. 313 - 322 (2007/10/02)

Perfluoroalkyl ether substituted silicon compounds of the type (CH3)nSi(RfORf)4-n (n=1-3) and HSi(RfORf)3 where RfORf=F(CF3)2COCF2CF2have been synthesized in good yields (64-81percent) through the reaction between the organolithium reagent RfORfLi and the corresponding silicon chloride.The stability of these compounds towards acid, base and aqueous media were studied and the ease of cleavage of the Si-RfORf bond was found to be in the order HSi(RfORf)3>CH3Si(RfORf)3>(CH3)2Si(RfORf)2>(CH3)3SiRfORf.The influence of the RfORf group on some properties of these compounds is also described.

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