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1-Propene, 1,1,3,3,3-pentafluoro-2-methyl-, also known as 2-methyl-1-pentene, is a halogenated hydrocarbon with the chemical formula C5H7F5. It is a colorless, volatile liquid with a pungent odor. 1-Propene, 1,1,3,3,3-pentafluoro-2-methyl- is characterized by the presence of five fluorine atoms and one methyl group attached to a propene backbone. It is synthesized through various chemical reactions, such as the fluorination of 2-methylpropene or the addition of fluorine to 2-methyl-1-butene. Due to its unique structure and properties, 1-Propene, 1,1,3,3,3-pentafluoro-2-methyl- has potential applications in the production of refrigerants, propellants, and as an intermediate in the synthesis of other fluorinated compounds. However, it is essential to handle this chemical with caution, as it may pose health and environmental risks due to its potential toxicity and persistence in the environment.

2253-00-1

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2253-00-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2253-00-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,5 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2253-00:
(6*2)+(5*2)+(4*5)+(3*3)+(2*0)+(1*0)=51
51 % 10 = 1
So 2253-00-1 is a valid CAS Registry Number.

2253-00-1SDS

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 1,1,3,3,3-pentafluoro-2-methylprop-1-ene

1.2 Other means of identification

Product number -
Other names 1,1,3,3,3-pentafluoro-2-methyl-1-propene

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:2253-00-1 SDS

2253-00-1Downstream Products

2253-00-1Relevant academic research and scientific papers

PROCESS FOR MAKING 1,1,1,4,4,4-HEXAFLUORO-2-BUTENE

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Page/Page column 8-9, (2009/10/22)

A process is disclosed for making 1,1,1,4,4,4-hexafluoro-2-butene. The process involves reacting 2,2-dichloro-1,1,1-trifluoroethane with copper in the presence of an amide solvent and 2,2'-bipyridine. A process is also disclosed for making 1,1,1,4,4,4-hexafluoro-2-butene. The process involves reacting 2,2-dichloro-1,1,1-trifluoroethane with copper in the presence of an amide solvent and a Cu(I) salt. A process is further disclosed for making 1,1,1,4,4,4-hexafluoro-2-butene. The process involves reacting 2,2-dichloro-1,1,1-trifluoroethane with copper in the presence of an amide solvent, 2,2'-bipyridine and a Cu(I) salt.

FLUOROBUTENE DERIVATIVES AND PROCESS FOR PRODUCING SAME

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Page 28, (2008/06/13)

The present invention provides novel compounds, 2, 4,4,4-tetrafluoro-1-butene and (E)- and (Z)-1,1,1,3-tetrafluoro-2 butenes. Furthermore, the present invention provides the following novel first and second processes for producing 2,4,4,4-tetrafluoro-1-butene, (E)- and (Z)-1,1,1,3-tetrafluoro-2-butenes, and 1,1,3-trifluorobutadiene. The first process is a process for producing 2,4,4,4-tetrafluoro-1-butene by heating 1,1,1,3,3-pentaflurobutane at from about 200°C to about 700°C. The second process is a process for producing (E)- and (Z)-1,1,1,3-tetrafluoro-2-butenes by bringing 1,1,1,3,3-pentafluorobutane with a base. By the first and second processes, it is possible to obtain respective target fluorobutenes with high selectivity. In third to fifth processes, 2,4,4,4-tetrafluoro-1-butene, (E)- and (Z)-1,1,1,3-tetrafluoro-2-butene, and 1,1,3,-trifluorobutadiene can be produced by heating 1,1,1,3,3-pentafluorobutane in the presence of a catalyst. This catalyst can be regenerated by the contact with a halogen-containing gas in sixth process.

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