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Benzene, (dichloromethyl)pentafluoro-, also known as 1,2-dichloro-2,2,2-trifluoroethane or CCl2FCF3, is a halogenated hydrocarbon compound consisting of a benzene ring with a dichloromethyl group and five fluorine atoms. This chemical is primarily used as a refrigerant, blowing agent, and fire extinguishing agent due to its low toxicity, high stability, and excellent thermodynamic properties. It is also employed in the production of various chemicals, such as fluoropolymers and pharmaceuticals. However, due to its potential environmental impact and contribution to ozone depletion, its use has been phased out in many countries under the Montreal Protocol.

652-30-2

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652-30-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 652-30-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,5 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 652-30:
(5*6)+(4*5)+(3*2)+(2*3)+(1*0)=62
62 % 10 = 2
So 652-30-2 is a valid CAS Registry Number.

652-30-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(dichloromethyl)-2,3,4,5,6-pentafluorobenzene

1.2 Other means of identification

Product number -
Other names pentafluorobenzylidene chloride

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:652-30-2 SDS

652-30-2Relevant academic research and scientific papers

Replacement of an oxygen atom by chlorine atoms in the reaction of pentafluorobenzaldehyde with CCl3-substituted compounds in the presence of AlCl3

Petrova, T. D.,Platonov, V. E.,Pokrovskii, L. M.

, p. 544 - 546 (2002)

The interaction of pentafluorobenzaldehyde with RCCl3 (R = Cl, Ph, C6F5) in the presence of threefold molar excess of AlCl3 proceeds with replacing the oxygen atom of the aldehyde group by two chlorine atoms from the CCl3 group and results in the formatio

Reductive transformations of organofluorine compounds: II. Hydrodechlorination of chloropolyfluoroarenes by the action of zinc

Krasnov,Platonov

, p. 1488 - 1499 (2007/10/03)

Polyfluoroarenes containing chlorine atoms in the aromatic ring and/or in the benzylic position undergo hydrodechlorination by the action of zinc in aqueous dimethylformamide. The use of Zn/Cu and addition of salts (NaCl, Na2SO4, NH4Cl) favor reductive dechlorination of the Carom - Cl bond. Polyfluorobenzotrichlorides react with excess zinc to give the corresponding CH3-substituted derivatives, otherwise CH2Cl- and CHCl2-containing compounds are formed. The reduction of C6F5CCl3 and C6F5CH2Cl with zinc in the presence of copper provides lower yields of the hydrodechlorination products and leads to formation of 1,2-bis(pentafluorophenyl)ethane.

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