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Chlorodifluoromethyl radical, with the chemical formula CHClF2, is a highly reactive and unstable molecule that plays a significant role in atmospheric chemistry. It is formed through the reaction of hydrochloric acid (HCl) with hydrofluoric acid (HF) or by the decomposition of chlorodifluoromethane (CHClF2), a common refrigerant and industrial chemical. This radical is of particular interest due to its potential involvement in the depletion of the ozone layer, as it can react with ozone molecules, leading to the formation of chlorine monoxide (ClO) and difluoromethyl (CHF2) radicals. The difluoromethyl radical can further react with oxygen to regenerate the chlorine radical, thus perpetuating the ozone-depleting cycle. Understanding the behavior and impact of chlorodifluoromethyl radicals is crucial for assessing the environmental consequences of certain industrial processes and for developing strategies to mitigate ozone depletion.

1691-89-0

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1691-89-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1691-89-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,9 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1691-89:
(6*1)+(5*6)+(4*9)+(3*1)+(2*8)+(1*9)=100
100 % 10 = 0
So 1691-89-0 is a valid CAS Registry Number.
InChI:InChI=1/CClF2/c2-1(3)4

1691-89-0SDS

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 chloro(difluoro)methane

1.2 Other means of identification

Product number -
Other names chlorodifluoromethyl radical

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:1691-89-0 SDS

1691-89-0Relevant academic research and scientific papers

Rate measurement of the reaction of CF2Cl radicals with O 2

Codnia, Jorge,Azcarate, Maria Laura

, p. 755 - 762 (2006)

We have studied the association reaction of the CF2Cl radicals with O2 in presence of N2. The infrared multiple photon dissociation (IRMPD) technique with a homemade TEA CO2 laser was used for the CF2Cl radical generation and the vibrational chemiluminiscence technique was set up for the study of the reaction kinetics. The time-resolved IR fluorescence of the vibrationally excited CF2O photoproduct was used to measure the disappearance rate of these radicals. A kinetic mechanism is presented to account for the rate of production of CF 2O*. The CF2Cl radical association reaction rate with O2, evidence of a direct channel of photoproduct formation and its reaction rate, and the CF2O* collisional deactivation rate have been obtained.

Time Resolved Studies of Intermediate Products in the Oxidation of HCFC 141b (CFCl2CH3)and HCFC (CF2ClCH3)

Moers,Hoffmann,Malms,Zellner

, p. 540 - 552 (2007/10/03)

The oxiueauve degradation of HCFC 14Sb (CFCl2CH3) and HCFC 142b (CF2C1CH3) in the presence of NO at T = 293 K and p = 50 mbar has been studied using laser pulse initiation combined with cw laser long path absorption/UF for the detection of OH and NO2. The absolute yield and temporal behaviour of these products have been found to be sensitive indicators for the reaction behaviour of the alkoxy radicals CFCl2CH2O and CF2ClCH2O, respectively. The rate coefficients for the reactions of the alkoxy radicals with O2 were determined to be k(CFCl2CH2O + O2-CFCl2CHO + HO2) = (2.0±1.0)× 10-15 cm3/s and k(CF2ClCH2O + O2→CF2CiCHO + HO2) = (2.5±1.5)× 10-15 cm3/s. Upper limits for the rate coefficients for unimolecular decomposition of the alkoxy radicals by C-C-bond fission of k(CFCl2CH2O + M→CFCl2 + CH2O-rM)≤ 1.0×103 s-1 and k(CF2ClCH2O + M→CF2Cl + CH2OJ-M)≤1.5×103s-1 were derived. We conclude from these data that CFCl2CHO and CF2ClCHO will be formed as the dominant primary carbonyl products in the oxidation of HCFC 141 b and 142b throughout the troposphere. Moreover, the rate coefficients for the reactions of the HCFCs with OH radicals at T = 293 K have been measured. The values k(CFCl2CH3 +OH→CFCl2CH2 + H2O) = (4.6 ±0.8)×10-15 cm3/s and k(CF2ClCH3 + OH→CF2ClCH2 + H2O) = (2.6±0.4)× 10-15cm3/s were obtained. VCH Verlagsgesel/schaft mbH, 1996.

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