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Cyclobutane, 1,1,2,2,3,4-hexafluoro- is a halogenated cyclobutane compound with the chemical formula C4F6H2. It is a colorless, volatile liquid with a molecular weight of 200.04 g/mol. Cyclobutane, 1,1,2,2,3,4-hexafluoro- is characterized by the presence of six fluorine atoms and two hydrogen atoms attached to a four-membered cyclic structure. Due to its unique structure and properties, it has potential applications in various fields, such as pharmaceuticals, agrochemicals, and materials science. It is also used as a solvent and a chemical intermediate in the synthesis of other fluorinated compounds. However, it is important to note that handling and disposal of Cyclobutane, 1,1,2,2,3,4-hexafluoro- should be done with caution, as it may have potential environmental and health risks.

377-95-7

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377-95-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 377-95-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,7 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 377-95:
(5*3)+(4*7)+(3*7)+(2*9)+(1*5)=87
87 % 10 = 7
So 377-95-7 is a valid CAS Registry Number.

377-95-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-1,2-dihydrohexafluorocyclobutane

1.2 Other means of identification

Product number -
Other names (+/-)-1,1,2,2,3r,4t-Hexafluor-cyclobutan

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:377-95-7 SDS

377-95-7Downstream Products

377-95-7Relevant academic research and scientific papers

Fluorination of fluoro-cyclobutene with high-valency metal fluoride

Mizukado, Junji,Matsukawa, Yasuhisa,Quan, Heng-Dao,Tamura, Masanori,Sekiya, Akira

, p. 79 - 84 (2007/10/03)

Fluorinations of 1,4,4-trifluorocyclobutene and 3,3,4,4- tetrafluorocyclobutene using high-valency metal fluorides such as CoF 3, MnF3, AgF2, CeF4 and KCoF 4, and elemental fluorine were examined. In these reactions with CoF3 and MnF3, vic-difluorination proceeded mainly. While, 1,4,4-trifluorocyclobutene yielded 3,3,4,4-tetrafluorocyclobutene, and 3,3,4,4-tetrafluorocyclobutene yielded 1,3,3,4,4-pentafluorocyclobutene mainly in the case of AgF2. The further fluorinated products were increased under severer conditions. Also, the plausible reaction mechanism was suggested.

Reductive dehalogenation of polyhalofluorocarbons with tributyltin hydride

Puy, Michael Van Der,Belter, Randolph K.,Borowski, Ralph J.,Ellis, Lois A. S.,Persichini, Phillip J.,et al.

, p. 59 - 64 (2007/10/02)

The reduction of polyhalofluorocarbons, including ClCF2CFClCF2Cl, (ClCF2CFCl)2, ICH2(CF2)3CH2I and vicinal dichloroperfluorocycloalkanes, with tributyltin hydride gave the corresponding hydrofluorocarbons in good to excellent yield.The results are compared with similar reductions with other reducing agents, and to tin hydride reductions of non-fluorinated analogs. - Keywords: Reductive dehalogenation; Polyfluorocarbons; Tributyltin hydride; NMR spectroscopy; Hydrofluorocarbons

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