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13453-52-6

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13453-52-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13453-52-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,5 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13453-52:
(7*1)+(6*3)+(5*4)+(4*5)+(3*3)+(2*5)+(1*2)=86
86 % 10 = 6
So 13453-52-6 is a valid CAS Registry Number.

13453-52-6SDS

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 monofluorocarbene

1.2 Other means of identification

Product number -
Other names fluorocarbene

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:13453-52-6 SDS

13453-52-6Relevant academic research and scientific papers

Emission from FCO in the Reactions of Ozone with Fluoroethenes

Toby, Sidney,Toby, Frina S.

, p. 4071 - 4073 (1981)

The gas-phase reactions of ozone with cis-1,2-difluoroethene, trans-1,2-difluoroethene, trifluoroethene, and chlorotrifluoroethene are all accompanied by light with a maximum intensity at approximately 425 nm.A partial vibrational analysis of this emission is presented and it is concluded that the emitting species is the FCO radical, as previously suggested.A comparison is made between the enthalpy changes of the primary reactions between ozone and the fluoroethenes and their correlation with the identity of the emitting species.The exothermicity of the reaction correlates with the chemiluminescent reaction channel.

Dissociations of Gas-Phase CHClF and CHCl2 Radicals and Cations following Collisional Electron Transfer. A Variable-Time Neutralization-Reionization and ab Initio Study

Sadilek, Martin,Turecek, Frantisek

, p. 224 - 232 (1996)

Variable-time neutralization-reionization mass spectrometry is used to generate CHClF(.) and CHCl2(.) radicals and to study their unimolecular dissociations within 0.4-4.1 μs.Loss of Cl(.) is a major dissociation of CHClF(.) following collisional neutrali

Photodissociation dynamics of trifluoroethylene at 157 nm excitation

Lin,Hsu,Hwang,Lee,Yang

, p. 10719 - 10726 (2007/10/03)

Photodissociation of trifluoroethylene (F2CCFH) at 157 nm has been investigated using photofragment translational spectroscopy. Four dissociation channels have been experimentally observed: molecular HF elimination, H atom elimination, F atom e

On the Reaction of CH2(a1A1) with HF

Wagener, R.,Wagner, H. Gg.

, p. 1096 - 1100 (2007/10/02)

The insertion reaction of singlet methylene CH2(a1A1) into the strongest element-hydrogen bond, H-F, is investigated.CH2(a1A1) is generated by pulsed UV-laser photolysis of CH2CO.Its removal is directly monitored via LIF-detection.The experiments are carried out under first order reaction conditions at temperatures T = 295, 380, and 485 K.Second order rate constants are determined from plots of first order rate constants versus the partial pressure of HF.The expression k1 = (5.5 +/- 1.5) * 1013 * (T/295 K)(-0.5 +/- 0.5) cm3/mol s is derived for the rate constant of the total depletion of CH2(a1A1 0,0,0) with HF.Thus at room temperature the reaction is slower than the analogous reactions with NH3, H2O and HCl.For the isotopically substituted CD2(a1A1 0,0,0) with HF the following rate expression is determined: k2 = (1.0 +/- 0.3) * 1014 (T/295 K)(-1.0 +/- 1.0) cm3/mol s.The reaction of vibrationally excited CH2(a1A1 0,0,0) with HF has a room temperature rate constant of k3 = (2.0 +/- 0.4) * 1014 cm3/mol s.Fluorocarbene CHF is detected as primary reaction product by LIF.Thermochemical considerations show that formation of CHF is the only exothermic reaction pathway besides physical quenching of CH2(a1A1).

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