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4,4,5,5,6,6,6-heptafluorohex-1-ene is a fluorinated organic compound with the molecular formula C6H3F7. It is a colorless liquid with a strong, pungent odor. This chemical is characterized by the presence of seven fluorine atoms and three hydrogen atoms, with the fluorine atoms being attached to the carbon chain in a specific pattern. It is used in various industrial applications, such as the production of fluoropolymers and as a chemical intermediate in the synthesis of other fluorinated compounds. Due to its highly fluorinated nature, it exhibits unique properties, such as resistance to heat, chemicals, and UV radiation, which make it valuable in specialized applications. However, it is also important to note that handling and disposal of such chemicals require careful consideration due to their potential environmental and health impacts.

2317-84-2

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2317-84-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2317-84-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,1 and 7 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2317-84:
(6*2)+(5*3)+(4*1)+(3*7)+(2*8)+(1*4)=72
72 % 10 = 2
So 2317-84-2 is a valid CAS Registry Number.

2317-84-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4,5,5,6,6,6-heptafluorohex-1-ene

1.2 Other means of identification

Product number -
Other names 4,4,5,5,6,6,6-heptafluoro-1-hexene

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:2317-84-2 SDS

2317-84-2Downstream Products

2317-84-2Relevant academic research and scientific papers

TRANSITION-METAL COMPLEX CATALYZED POLYFLUOROALKYLATION. II. NOVEL AND CONVENIENT ROUTE TO 3-POLYFLUOROALKYLPROP-1-ENES THROUGH THE REACTION OF POLYFLUOROALKYL HALIDES WITH ALLYLSILANES

Fuchikami, Takamasa,Ojima, Iwao

, p. 307 - 308 (1984)

The reactions of polyfluoroalkyl halides with allylsilanes catalyzed by iron or ruthenium carbonyl complexes give 3-polyfluoroalkylprop-1-enes in good yields under mild conditions.

Synthesis of fluorinated brassinosteroids based on alkene cross-metathesis and preliminary biological assessment

Eignerová, Barbara,Slavíkova, Barbora,Budě?ínsky, Milo?,Dra?ínsky, Martin,Klepetá?ov?a, Blanka,?t'Astná, Eva,Kotora, Martin

supporting information; experimental part, p. 5753 - 5757 (2010/03/24)

Three types of brassinosteroid analogues with perfluoroalkylated side chains were synthesized by using alkene cross-metathesis of a brassinosteroid derivative bearing a terminal alkene moiety with different (perfluoroalkyl) propenes. The presence of the d

Perfluoroalkylation through cross-metathesis between alkenes and (perfluoroalkyl)propenes

Eignerova, Barbara,Dracinsky, Martin,Kotora, Martin

supporting information; experimental part, p. 4493 - 4499 (2009/04/19)

A new approach to perfluoroalkylated compounds based on cross-metathesis between perfluoropropenes and terminal alkenes has been developed. The reaction is catalysed with high efficiency and selectivity by the Hoveyda-Grubbs second-generation catalyst under mild reaction conditions. The method is applicable to a wide range of compounds, such as vinylaromatics, isoprenoids and saccharides. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.

Synthesis of functionalized long-chain perfluoroalkanes from methyl halodifluoroacetates: a process of difluorocarbene insertion into copper-carbon bonds

Su, De-Bao,Duan, Jian-Xing,Yu, An-Juan,Chen, Qing-Yun

, p. 11 - 14 (2007/10/02)

Treatment of XCF2CO2Me (X = Cl, Br) with organic halides in the presence of KF and catalytic amounts of CuI at 80-120 deg C for 3-8 h in DMF gave long-chain perfluoroalkylated compounds which are considered to be former by the insertions of CF2(..) into carbon-copper bonds.

Process for preparing polyfluoroalkyl-substituted compounds

-

, (2008/06/13)

A process for preparing a perfluoroalkyl-substituted compound is disclosed. The process comprises reacting a halopolyfluoroalkane having 1 to 20 carbon atoms with a compound selected from the group consisting of (1) a substituted or unsubstituted ethylene, (2) a substituted or unsubstituted acetylene and (3) a substituted or unsubstituted allylsilane, in the presence of a metal-carbonyl complex of the metal of the Group VIII of the Periodic Table. Alternatively, the reaction between the halopolyfluoroalkane and the substituted or unsubstituted allylsilane is effected under radical generating condition.

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