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760-42-9

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760-42-9 Usage

General Description

1,1,1,2,4,4,4-Heptafluoro-2-butene is a colorless, non-toxic and non-flammable chemical compound. It is commonly used as a refrigerant and in the production of fluoropolymer resins. 1,1,1,2,4,4,4-HEPTAFLUORO-2-BUTENE has a high global warming potential and is considered to be a greenhouse gas, contributing to climate change. Additionally, it is an ozone-depleting substance, with the potential to harm the atmosphere. Due to its environmental impact, efforts are being made to find alternative compounds and technologies to replace 1,1,1,2,4,4,4-heptafluoro-2-butene in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 760-42-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,6 and 0 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 760-42:
(5*7)+(4*6)+(3*0)+(2*4)+(1*2)=69
69 % 10 = 9
So 760-42-9 is a valid CAS Registry Number.
InChI:InChI=1/C4HF7/c5-2(4(9,10)11)1-3(6,7)8/h1H/b2-1-

760-42-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-1,1,1,2,4,4,4-heptafluorobut-2-ene

1.2 Other means of identification

Product number -
Other names 1,1,1,2,4,4,4-Heptafluoro-2-butene

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:760-42-9 SDS

760-42-9Relevant articles and documents

MANUFACTURING METHOD OF PERFLUOROCYCLOALKENE COMPOUND

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Paragraph 0083-0091, (2020/05/14)

PROBLEM TO BE SOLVED: To obtain a perfluorocycloalkene compound high in conversion ratio of a reaction at high yield and high selectivity. SOLUTION: A perfluorocycloalkene compound represented by (1), where R1 to R4 are same or different, and represent a fluorine atom or a perfluoroalkadiene compound, is obtained by conducting a cyclization reaction of a perfluoroalkanediene compound represented by CR12=CR2-CR3=CR42, where R1 to R4 are same or different and represent a fluorine atom or a perfluoroalkyl group. The cyclization reaction can be conducted in presence of a catalyst, by a gas phase continuous flow type, or by the gas phase continuous flow type in presence of the catalyst. SELECTED DRAWING: None COPYRIGHT: (C)2020,JPOandINPIT

Preparation method of 1,1,1,2,4,4,4-heptafluoro-2-butene

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Paragraph 0027; 0028; 0229; 0030; 0031; 0036; 0041, (2019/01/07)

The invention discloses a preparation method of 1,1,1,2,4,4,4-heptafluoro-2-butene. The method uses hexachlorobutadiene and hydrogen fluoride as raw materials and uses a chromium-based catalyst as a fluorine-chlorine exchange catalyst to form the 1,1,1,2,4,4,4-heptafluoro-2-butene under gas phase conditions through a plurality of gas-phase catalytic reactions. Compared with the prior art, the preparation method of the 1,1,1,2,4,4,4-heptafluoro-2-butene provided by the invention has the following advantages: 1, the gas phase fluorination method adopted in the method is a cycle fluorination method, has less three industrial wastes (waste water, waste gases and solid waste), and greatly reduces the production costs; 2, the method can realize rapid and multiple-cycle fluorination, improve a product yield, and have simple separation and purification of the product; and 3, the method has the advantages of cheap raw materials, convenient sources and simple operation, and is suitable for industrialized production.

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