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Cyclohexane, undecafluoromethoxy-, also known as perfluoromethylcyclohexane, is a chemical compound with the molecular formula C7H3F11O. It is a colorless, odorless, and non-toxic liquid that is insoluble in water. Cyclohexane, undecafluoromethoxy- is characterized by its unique structure, where a cyclohexane ring is substituted with an undecafluoromethoxy group (CF3O-). It is primarily used as a solvent in various chemical reactions and processes, particularly in the electronics and semiconductor industries, due to its low dielectric constant, high thermal stability, and excellent dielectric properties. Additionally, it has potential applications in the development of new materials and as a component in specialty lubricants.

4943-08-2

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4943-08-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4943-08-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,4 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4943-08:
(6*4)+(5*9)+(4*4)+(3*3)+(2*0)+(1*8)=102
102 % 10 = 2
So 4943-08-2 is a valid CAS Registry Number.

4943-08-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl undecafluorocyclohexyl ether

1.2 Other means of identification

Product number -
Other names 1,1,2,2,3,3,4,4,5,5,6-Undecafluoro-6-methoxy-cyclohexane

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:4943-08-2 SDS

4943-08-2Downstream Products

4943-08-2Relevant academic research and scientific papers

REACTION OF POLYFLUORINATED DERIVATIVES OF BENZENE CONTAINING HYDROGEN ATOMS IN THE SIDE CHAIN WITH VANADIUM PENTAFLUORIDE

Avramenko, A. A.,Bardin, V. V.,Karelin, A. I.,Krasil'nikov, V. A.,Tushin, P. P.,et al.

, p. 2318 - 2323 (2007/10/02)

The treatment of C6F5R (R=CH3, CH2F, CHF2) compounds with vanadium pentafluoride at -25 to -30 deg C leads to a 1-R-heptafluoro-1,4-cyclohexadienes, 1-R-nonafluorocyclohexenes, and products form fluorination of the side chain.Fluorination of the anisole derivatives C6F5OCH3 and C6F5OCHF2 only takes place in the aromatic ring.

POLYFLUORO-1,2-EPOXY-ALKANES AND -CYCLOALKANES. PART I. PREPARATION OF SOME POLYFLUORO-1,2-EPOXYCYCLOHEXANES

Coe, Paul L.,Mott, Andrew W.,Tatlow, John Colin

, p. 243 - 254 (2007/10/02)

Polyfluorocyclohexenes with hydrogen, bromine, and methoxy substituents yielded the corresponding 1,2-epoxides when treated with aqueous sodium hypochlorite containing some acetonitrile. 4,5-Dibromooctafluoro-1,2-epoxycyclohexane was debrominated with zin

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