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813-75-2

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813-75-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 813-75-2 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 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 813-75:
(5*8)+(4*1)+(3*3)+(2*7)+(1*5)=72
72 % 10 = 2
So 813-75-2 is a valid CAS Registry Number.

813-75-2SDS

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 1,3-difluoro-2,2-difluoropropane

1.2 Other means of identification

Product number -
Other names 1,2,2,3-tetrafluoropropane

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:813-75-2 SDS

813-75-2Downstream Products

813-75-2Relevant articles and documents

Fluorination of propane and propene over cobalt(III) trifluoride and potassium tetrafluorocobaltate(III)

Burdon, James,Garnier, Laurent,Powell, Richard L.

, p. 625 - 632 (2007/10/03)

Fluorination of propane and propene over cobalt(III) fluoride and potassium tetrafluorocobaltate(III) gave complex mixtures of products which have been identified to the 0.5percent level.The reactions are valuelles for preparative purposes.The mechanism of the fluorinations is not a simple F-for-H replacement, but requires an initial conversion of propane into propene followed by carbocation- and radical mediated reactions: the carbocations can be quenched by fluoride ions, rearrange and eliminate, and the radicals can be oxidised to carbocations or quenched by fluorine atoms.Radical quenching tends to predominate late in the fluoronation and carbocation reactions at the beginning.

Process for producing a 2,2-difluoropropane

-

, (2008/06/13)

A process for producing a 2,2-difluoropropane of the following formula (2), which comprises fluorinating a chlorine-containing 2,2-halogenopropane of the following formula (1) by hydrogen fluoride or a fluorinating agent: wherein a, b, c and x are integers satisfying the following conditions:

REACTION OF SULPHUR TETRAFLUORIDE WITH HALOGENATED ACETONES. THE EVIDENCE FOR PARTICIPATION OF FLUOROCARBOCATIONS

Wielgat, Jerzy,Domagala, Zdzislaw,Kolinski, Ryszard A.

, p. 182 (2007/10/02)

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