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3,3,4,4,5,5,6,6-Octafluorocyclohexene is a halogenated cycloalkene compound characterized by the presence of eight fluorine atoms attached to a six-carbon ring structure. This molecule is known for its unique electronic properties and chemical stability due to the strong electronegativity of fluorine atoms. It is often used as an intermediate in the synthesis of various fluorinated compounds, such as pharmaceuticals and specialty chemicals. The octafluorocyclohexene molecule exhibits a high degree of thermal and chemical resistance, making it a valuable building block in the development of new materials with enhanced properties.

775-40-6

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775-40-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 775-40-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,7 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 775-40:
(5*7)+(4*7)+(3*5)+(2*4)+(1*0)=86
86 % 10 = 6
So 775-40-6 is a valid CAS Registry Number.

775-40-6SDS

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 3,3,4,4,5,5,6,6-octafluorocyclohexene

1.2 Other means of identification

Product number -
Other names CYCLOHEXENE,3,3,4,4,5,5,6,6-OCTAFLUORO

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:775-40-6 SDS

775-40-6Relevant academic research and scientific papers

Fluorination of tetrafluorobenzenes C6HF4R with XeF2

Bardin,Shchegoleva,Frohn

, p. 153 - 159 (2007/10/03)

Replacement of hydrogen by fluorine and addition of fluorine atoms to the aromatic ring were found in the reaction of XeF2 with 1-R-2,3,4,5-tetrafluorobenzene (R = H, F, Br, NO2) or 1-R-2,3,4,6-tetrafluorobenzene (R = H, CF3) in HF or CH2Cl2-BF3·OEt2. Only fluorine addition took place in the case of 1-R-2,3,5,6-tetrafluorobenzenes (R = H, Br, CF3) or 1-Br-2,3,4,6-tetrafluorobenzene. The role of cation radicals as reactive intermediates is discusseed.

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