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Perfluoro(N-iso-propylmorpholine), also known as 1-(1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctyl)-4-methylmorpholine, is a perfluorinated organic compound characterized by its unique structure and properties. It is a colorless liquid with a low melting point and high boiling point, and it is insoluble in water. This chemical is primarily used as a surfactant in various industrial applications, such as in the production of fluoropolymers, as a wetting agent, and in fire-fighting foams. Due to its perfluorinated nature, it exhibits excellent chemical and thermal stability, making it suitable for use in harsh environments. However, it is important to note that perfluorinated compounds, including perfluoro(N-iso-propylmorpholine), have raised environmental concerns due to their potential persistence in the environment and bioaccumulation in living organisms.

1600-71-1

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1600-71-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1600-71-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,0 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1600-71:
(6*1)+(5*6)+(4*0)+(3*0)+(2*7)+(1*1)=51
51 % 10 = 1
So 1600-71-1 is a valid CAS Registry Number.

1600-71-1Downstream Products

1600-71-1Relevant 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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