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303-04-8

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303-04-8 Usage

Chemical Properties

clear colorless liquid

General Description

The pure cis- and trans-isomers of 2,3-dichlorohexafluoro-2-butene were separated when 2,3-dichlorohexafluoro-2-butene (mixture of cis and trans) reacted with dry diglyme and sodium borohydride and was hydolyzed. The isomers were purified by preparative vapor phase chromatography technique.

Check Digit Verification of cas no

The CAS Registry Mumber 303-04-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,0 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 303-04:
(5*3)+(4*0)+(3*3)+(2*0)+(1*4)=28
28 % 10 = 8
So 303-04-8 is a valid CAS Registry Number.
InChI:InChI=1/C4Cl2F6/c5-1(3(7,8)9)2(6)4(10,11)12/b2-1-

303-04-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-DICHLOROHEXAFLUORO-2-BUTENE

1.2 Other means of identification

Product number -
Other names 2,3-DICHLOROHEXAFLUOROBUT-2-ENE

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:303-04-8 SDS

303-04-8Relevant articles and documents

Gas-phase continuous synthesis method of cis-1,1,1,4,4,4-hexafluoro-2-butene

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Paragraph 0026-0028; 0031-0033; 0036-0038; 0041-0043; 0046, (2020/01/03)

The invention discloses a gas-phase continuous synthesis method of cis-1,1,1,4,4,4-hexafluoro-2-butene. The method includes the following preparation steps: (1) mixing 1,1,1-trifluorotrichloroethane with hydrogen for a reaction so as to obtain a product stream I, transferring the product stream I to a first separation tower, absorbing the mixed product stream obtained at the tower top through a HCl absorption tower, and returning the mixed product stream to a reactor I so as to obtain 1,1,1,4,4,4-hexafluoro-2,3-dichloro-2-butene in the tower kettle; (2) transferring the tower kettle liquid obtained in the step (1) to a preheater II, introducing hydrogen at the same time, performing mixing and preheating until 200 DEG C, transferring the preheated mixture to a reactor II, performing a hydrodechlorination reaction under the action of a catalyst so as to obtain a product stream II, transferring the product stream II to a second separation tower, and circulating the tower kettle liquid tothe reactor II; and (3) transferring the tower top product obtained in the step (2) to a preheater III, performing preheating to 260 DEG C, transferring the preheated product to a reactor III, performing an isomerization reaction under the action of a catalyst so as to obtain a product stream III, transferring the product stream III to a third separation tower so as to obtain cis-1 1,1,4,4,4-hexafluoro-2-butene in the tower kettle.

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.

PROCESS FOR THE PREPARATION OF FLUORINATED CIS-ALKENE

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Page/Page column 4, (2011/12/12)

Disclosed is a process for the preparation of fluorine-containing olefins comprising contacting a chlorofluoroalkane with hydrogen in the presence of a catalyst at a temperature sufficient to cause replacement of the chlorine substituents of the chlorofluoroalkane with hydrogen to produce a fluorine-containing olefin. Also disclosed are catalyst compositions for the hydrodechlorination of chlorofluoroalkanes comprising copper metal deposited on a support, and comprising palladium deposited on calcium fluoride, poisoned with lead and reducing the in the presence or absence of a dehydrochlorination catalyst under conditions effective to form a product stream comprising cis-1,1,1,4,4,4-hexafluoro-2-butene (HFO-1336).