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Perfluoro(N-iso-propylpiperidine) is a synthetic chemical compound characterized by its unique structure and properties. It is a perfluorinated derivative of N-iso-propylpiperidine, where all hydrogen atoms in the molecule have been replaced by fluorine atoms. This modification significantly enhances the compound's chemical stability, thermal resistance, and non-stick properties. Perfluoro(N-iso-propylpiperidine) is often used in various industrial applications, such as in the production of high-performance lubricants, surfactants, and polymers. Due to its resistance to degradation and unique properties, it is also employed in specialized coatings and materials for aerospace, electronics, and medical industries. However, concerns about its environmental persistence and potential health impacts have led to increased scrutiny and regulations regarding its use and disposal.

3710-77-8

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3710-77-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3710-77-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,1 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3710-77:
(6*3)+(5*7)+(4*1)+(3*0)+(2*7)+(1*7)=78
78 % 10 = 8
So 3710-77-8 is a valid CAS Registry Number.

3710-77-8Downstream Products

3710-77-8Relevant academic research and scientific papers

The electrochemical fluorination of N-containing carboxylic acids (Part 4). Fluorination of methyl 3-dialkylamino-isobutyrates and methyl 3-dialkylamino-n-butyrates

Abe, Takashi,Fukaya, Haruhiko,Hayashi, Eiji,Hayakawa, Yoshio,Nishida, Masakazu,Baba, Hajime

, p. 193 - 202 (2007/10/02)

Several methyl esters of 3-dialkylamino-substituted n- and isobutyric acids have been subjected to electrochemical fluorination to give the corresponding perfluoroacid fluorides.Dimethyl, diethyl, pyrrolidino, morpholino, piperidino and N-methylpiperazino groups were investigated as dialkylamino substituents.The structure/yield relationship was evaluated both in terms of the structure of the acid and the kind of amino group, respectively.Better yields of perfluoroacid fluorides were obtained from methyl esters having isobutyric acid skeletons than those having n-butyric acid groups, and from the acids containing cyclic amino groups than those containing acyclic ones.

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