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422-52-6

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422-52-6 Usage

Physical state

Colorless, non-flammable gas

Uses

a. Formerly used as a refrigerant
b. Formerly used as a propellant in aerosol cans

Environmental impact

a. Harmful to the ozone layer
b. Phased out under the Montreal Protocol
c. Considered a greenhouse gas
d. Potential contributor to global warming

Health effects

a. Causes irritation to the eyes
b. Causes irritation to the skin
c. Can cause respiratory effects
d. Can cause neurological effects

Legal status

a. Production and use heavily restricted in many countries
b. Restrictions aimed at mitigating environmental and health impacts

Check Digit Verification of cas no

The CAS Registry Mumber 422-52-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,2 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 422-52:
(5*4)+(4*2)+(3*2)+(2*5)+(1*2)=46
46 % 10 = 6
So 422-52-6 is a valid CAS Registry Number.
InChI:InChI=1/C3HCl4F3/c4-1(5)2(8,9)3(6,7)10/h1H

422-52-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,3,3-tetrachloro-1,2,2-trifluoropropane

1.2 Other means of identification

Product number -
Other names 1-Hydro-2,2,3-trifluor-tetrachlor-propan

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:422-52-6 SDS

422-52-6Relevant articles and documents

19F nuclear magnetic resonance studies of halogenated propanes

Tanuma, T.,Ohnishi, K.,Okamoto, H.,Miyajima, T.,Morikawa, S.

, p. 259 - 284 (2007/10/02)

The relationship between 19F chemical shifts in halogenated propanes and their structures are elucidated using MNDO calculations to determine the population of rotamers.The pairs of atom gauche to a fluorine atom and van der Waals interaction between the two terminal substituents are responsible for the 19F chemical shifts.The differences among chemical shifts in diastereomers are also discussed in terms of the conformation of molecule.

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