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422-54-8

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422-54-8 Usage

General Description

1,3,3-trichloro-1,1,2,2-tetrafluoropropane, also known as CFC-113a, is a chemical compound that belongs to the family of chlorofluorocarbons (CFCs). It is a colorless, odorless gas with the chemical formula C2Cl3F4. CFC-113a was used as a refrigerant and in the production of foam-blowing agents, but it has been phased out due to its ozone-depleting properties. It is a potent greenhouse gas and poses a significant threat to the ozone layer, contributing to the depletion of the Earth's protective ozone layer. As a result of international regulations such as the Montreal Protocol, the production and use of 1,3,3-trichloro-1,1,2,2-tetrafluoropropane have been largely discontinued in favor of more environmentally friendly alternatives.

Check Digit Verification of cas no

The CAS Registry Mumber 422-54-8 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 422-54:
(5*4)+(4*2)+(3*2)+(2*5)+(1*4)=48
48 % 10 = 8
So 422-54-8 is a valid CAS Registry Number.
InChI:InChI=1/C3HCl3F4/c4-1(5)2(7,8)3(6,9)10/h1H

422-54-8Relevant articles and documents

PROCESS FOR REFINING HCFC-224ca AND/OR CFO-1213ya, PROCESS FOR PRODUCING HCFC-224ca, AND PROCESS FOR PRODUCING CFO-1213ya

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Paragraph 0121; 0122, (2019/12/04)

PROBLEM TO BE SOLVED: To provide a process in which a difficult-to-separate HCFC-224ab can easily be removed and HCFC-224ca and/or CFO-1213ya can be produced with high purity and high yield. SOLUTION: Provided is a process for refining HCFC-224ca and/or CFO-1213ya, comprising a step of removing at least a portion of said HCFC-224ab from a mixture containing 1,1,3-trichloro-2,2,3,3-tetrafluoropropane (HCFC-224ca) and/or 1,1,3-trichloro-2,3,3-trifluoropropene (CFO-1213ya) and 1,2,2-trichloro-1,1,3,3-tetrafluoropropane (HCFC-224ab). SELECTED DRAWING: None COPYRIGHT: (C)2019,JPOandINPIT

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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