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Cyclohexanesulfonyl fluoride, 1,2,2,3,3,4,5,5,6,6-decafluoro-4-(trifluoromethyl)-, is a complex organic compound with the chemical formula C7H3F13O2S. It is a derivative of cyclohexanesulfonyl fluoride, featuring ten fluorine atoms and a trifluoromethyl group attached to the cyclohexane ring. Cyclohexanesulfonyl fluoride, 1,2,2,3,3,4,5,5,6,6-decafluoro-4-(trifluoromethyl)- is known for its unique properties, such as high reactivity and stability, which make it useful in various chemical reactions and applications, particularly in the synthesis of fluorinated compounds. Due to its highly fluorinated nature, it may also have potential uses in specialized industrial processes or as a reagent in advanced chemical research.

1478-14-4

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1478-14-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1478-14-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,7 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1478-14:
(6*1)+(5*4)+(4*7)+(3*8)+(2*1)+(1*4)=84
84 % 10 = 4
So 1478-14-4 is a valid CAS Registry Number.

1478-14-4SDS

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 perfluoro-4-methylcyclohexanesulfonylfluoride

1.2 Other means of identification

Product number -
Other names Perfluor-4-methylcyclohexansulfonylfluorid

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 -
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More Details:1478-14-4 SDS

1478-14-4Relevant academic research and scientific papers

THE ELECTROCHEMICAL FLUORINATION OF ORGANIC COMPOUNDS: FURTHER DATA IN SUPPORT OF THE ECbECN MECHANISM

Gambaretto, G. P.,Napoli, M.,Conte, L.,Scipioni, A.,Armelli, R.

, p. 149 - 156 (2007/10/02)

Data in support of the four-stage mechanism ECbECN result from the electrochemical fluorination of some acyl halides (benzoyl, n-butyryl and iso-butyryl, benzenesulphonyl and p-toluenesulphonyl chlorides) and amines (tripropylamine and N-methylmorpholine).

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