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1,1-dichloro-1,2,2-trifluoro-ethane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

812-04-4

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812-04-4 Usage

Reactivity Profile

1,1-dichloro-1,2,2-trifluoro-ethane is chemically inert in many situations, but can react violently with strong reducing agents such as the very active metals and the active metals. They suffer oxidation with strong oxidizing agents and under extremes of temperature.

Check Digit Verification of cas no

The CAS Registry Mumber 812-04-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,1 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 812-04:
(5*8)+(4*1)+(3*2)+(2*0)+(1*4)=54
54 % 10 = 4
So 812-04-4 is a valid CAS Registry Number.

812-04-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-dichloro-1,2,2-trifluoroethane

1.2 Other means of identification

Product number -
Other names 1,1,2-trifluoro-2,2-dichloroethane

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:812-04-4 SDS

812-04-4Relevant articles and documents

Isomerization reaction of dichlorotrifluoroethane

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Paragraph 0022-0035, (2019/12/25)

The invention discloses an isomerization reaction of dichlorotrifluoroethane. The reaction uses 2,2-dichloro-1,1,1-trifluoroethane as a raw material, and 1,2-dichloro-1,1,2-trifluoroethane (R123a) and1,1-dichloro-1,2,2-Trifluoroethane (R123b) are prepared under the action of an isomerization catalyst, wherein the isomerization catalyst is a mixture of AlF3 and AlCl3. The reaction has the advantages of simple process, strong operability, low cost, and the like.

Selective reduction of halopolyfluorocarbons by organosilicon hydrides

Petrov, Viacheslav A.

, p. 7294 - 7297 (2007/10/03)

It is demonstrated that silicon hydrides can be used for reduction of polyfluorinated halocarbons. For example, the reaction between CF3CCl2F and excess triethylsilane, catalyzed by benzoyl peroxide, leads to the formation of a mixture containing CF3CHClF (major), CF3CH2F, and ClSi(C2H5)3. On the other hand, the reaction of chlorofluoroalkanes, containing an internal -CCl2- group readily proceeds with reduction of both chlorines, leading to compounds such as (CF3)2CH2 and CF3CH2C2F5. In contrast to chlorofluoroalkanes, bromofluoroalkanes are much more reactive and reaction with hydrosilane rapidly proceeds without the catalyst at elevated temperature.

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